Page last updated: 2024-10-17

methylmalonic acid and Pregnancy

methylmalonic acid has been researched along with Pregnancy in 118 studies

Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.

Pregnancy: The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH.

Research Excerpts

ExcerptRelevanceReference
"Despite participation in overlapping metabolic pathways, the relationship between choline and vitamin B-12 has not been well characterized especially during pregnancy."9.30Maternal choline supplementation alters vitamin B-12 status in human and murine pregnancy. ( Bae, S; Caudill, MA; Jiang, X; King, JH; Klatt, KC; Kwan, STC; Malysheva, OV; Roberson, MS; Yan, J, 2019)
"Combined methylmalonic acidemia and homocystinuria, cblC type, is an inborn error of intracellular cobalamin metabolism with a wide spectrum of clinical manifestations that is stated to be the most common inherited disorder of cobalamin metabolism."8.88Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management. ( Carrillo-Carrasco, N; Chandler, RJ; Venditti, CP, 2012)
"Fasting plasma total homocysteine (tHcy) during pregnancy and low cobalamin status during early pregnancy are associated with mid-childhood metabolic score and its components in the offspring."8.31Pregnancy homocysteine and cobalamin status predict childhood metabolic health in the offspring. ( Ballesteros, M; Cavallé-Busquets, P; Fernandez-Ballart, J; Grifoll, C; Masana, L; Murphy, MM; Ornosa-Martin, G; Ramos-Rodriguez, C; Rojas-Gómez, A; Solé-Navais, P; Ueland, PM, 2023)
"Combined methylmalonic acidemia and homocystinuria, cobalamin C type (cblC defect) is the most common inborn error of cobalamin metabolism, and different approaches have been applied to its prenatal diagnosis."8.02Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type. ( Chen, T; Gong, Z; Gu, X; Han, L; Liang, L; Qiu, W; Wang, L; Xiao, B; Xu, F; Ye, J; Zhang, H; Zhu, H, 2021)
"Plasma levels of folate, cobalamin, pyridoxal 5'-phosphate (vitamin B6), riboflavin, and the metabolic markers total homocysteine, methylmalonic acid and 3-hydro-xykynurenine were measured in pregnancy week 18 and related to reported intake of folic acid from 4 weeks prior to conception throughout week 18 in 2911 women from the Norwegian Mother and Child Cohort Study (MoBa) conducted by the Norwegian Institute of Public Health."7.79Maternal B vitamin status in pregnancy week 18 according to reported use of folic acid supplements. ( Bjørke-Monsen, AL; Magnus, P; Midttun, Ø; Nilsen, RM; Reichborn-Kjennerud, T; Roth, C; Stoltenberg, C; Susser, E; Ueland, PM; Vollset, SE, 2013)
"Hyperhomocysteinemia is a risk factor in obstetrical complications such as pre-eclampsia, 'hemolysis, elevated liver enzymes, low platelet' (HELLP)-syndrome and placental insufficiency."7.72Alteration of homocysteine catabolism in pre-eclampsia, HELLP syndrome and placental insufficiency. ( Geisel, J; Herrmann, W; Hübner, U; Koch, I; Obeid, R; Retzke, U, 2004)
"We report on a favourable pregnancy in a woman affected by mut- methylmalonic acidaemia."7.71Successful pregnancy in a woman with mut- methylmalonic acidaemia. ( Baiocco, F; Boenzi, S; Deodato, F; Dionisi-Vici, C; Rizzo, C; Sabetta, G, 2002)
"Prenatal diagnosis for combined methylmalonic aciduria and homocystinuria was performed in five at-risk pregnancies by determination of methylmalonic acid (MMA) and total homocysteine (Hcy) in amniotic fluid supernatant."7.70Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria. ( Chadefaux-Vekemans, B; Garcia, MJ; Jakobs, C; Kamoun, P; Merinero, B; Pérez-Cerdá, C; Tonetti, C; Ugarte, M; Zittoun, J, 1998)
"Methylmalonic acidaemia is an inborn error of metabolism characterized by recurrent episodes of life-threatening ketoacidosis."7.70Successful pregnancy in severe methylmalonic acidaemia. ( Desnick, RJ; Eddleman, K; Gaddipati, S; Sansaricq, C; Snyderman, SE; Wasserstein, MP, 1999)
"The role of folic acid in the primary prevention of neural tube defects (NTDs) is well established."7.69Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects. ( Adams, MJ; Cheek, JE; Haddow, JE; Henry, JP; Khoury, MJ; Knight, GJ; Scanlon, KS; Stabler, SP; Stevenson, RE; Sylvester, GC, 1995)
"In a pregnant woman, who had given birth to a child with methylmalonic acidaemia previously, urinary methylmalonate was measured at various intervals in the second half of the pregnancy."7.66Methylmalonate excretion in a pregnancy at risk for methylmalonic acidaemia. ( Bakker, HD; Duran, M; van Gennip, AH; Wadman, SK, 1978)
"Methylmalonic aciduria is treated with a natural protein-restricted diet with adequate energy intake to sustain metabolic balance."5.62Dietary Treatment from Birth to Pregnancy in a Woman with Methylmalonic Aciduria. ( Kowalik, A; MacDonald, A; Sykut-Cegielska, J, 2021)
"Methylmalonic Acidurias (MMAs) are a group of inborn errors of metabolism (IEMs), specifically of propionate catabolism characterized by gastrointestinal and neurometabolic manifestations resulting from a deficiency in the function of methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and cobalamin metabolism."5.56A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy. ( Brindisino, P; Cicalini, I; Consalvo, A; De Laurenzi, V; Dionisi-Vici, C; Gasparroni, G; Gazzolo, D; Pieragostino, D; Rizzo, C; Rossi, C; Semeraro, D; Valentinuzzi, S; Zucchelli, M, 2020)
"Presently pregnancy is no more exceptional in women with metabolic diseases."5.39Pregnancy in a methylmalonic acidemia patient with kidney transplantation: a case report. ( Bellelli, E; Carducci, C; Elli, M; Gentile, I; Labriola, D; Lubrano, R; Paoli, S; Pérez, B; Santagata, S; Ugarte, M, 2013)
"Despite participation in overlapping metabolic pathways, the relationship between choline and vitamin B-12 has not been well characterized especially during pregnancy."5.30Maternal choline supplementation alters vitamin B-12 status in human and murine pregnancy. ( Bae, S; Caudill, MA; Jiang, X; King, JH; Klatt, KC; Kwan, STC; Malysheva, OV; Roberson, MS; Yan, J, 2019)
"Methylmalonic aciduria is a rare metabolic disorder of amino acid metabolism that is characterized by accumulation of large amounts of methylmalonic acid in the blood and urine."5.29Methylmalonic aciduria in pregnancy: a case report. ( Diss, E; Iams, J; Reed, N; Roe, C; Roe, DS, 1995)
"Combined methylmalonic acidemia and homocystinuria, cblC type, is an inborn error of intracellular cobalamin metabolism with a wide spectrum of clinical manifestations that is stated to be the most common inherited disorder of cobalamin metabolism."4.88Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management. ( Carrillo-Carrasco, N; Chandler, RJ; Venditti, CP, 2012)
"Although early epidemiologic studies showed a protective effect of adequate maternal folic acid (FA) status against neural tube defects (NTDs), the role of adequate vitamin B-12 nutrition in the putative reduction of NTD frequency has remained uncertain."4.85Vitamin B-12 and neural tube defects: the Canadian experience. ( Cole, DE; Ray, JG; Thompson, MD, 2009)
"Fasting plasma total homocysteine (tHcy) during pregnancy and low cobalamin status during early pregnancy are associated with mid-childhood metabolic score and its components in the offspring."4.31Pregnancy homocysteine and cobalamin status predict childhood metabolic health in the offspring. ( Ballesteros, M; Cavallé-Busquets, P; Fernandez-Ballart, J; Grifoll, C; Masana, L; Murphy, MM; Ornosa-Martin, G; Ramos-Rodriguez, C; Rojas-Gómez, A; Solé-Navais, P; Ueland, PM, 2023)
"Combined methylmalonic acidemia and homocystinuria, cobalamin C type (cblC defect) is the most common inborn error of cobalamin metabolism, and different approaches have been applied to its prenatal diagnosis."4.02Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type. ( Chen, T; Gong, Z; Gu, X; Han, L; Liang, L; Qiu, W; Wang, L; Xiao, B; Xu, F; Ye, J; Zhang, H; Zhu, H, 2021)
"In the longitudinal Reus-Tarragona Birth Cohort study from <12 gestational weeks throughout pregnancy, fasting plasma and red blood cell (RBC) folate, plasma cobalamin, holotranscobalamin (holoTC), methylmalonic acid (MMA), total homocysteine (tHcy), hemoglobin, mean cell volume (MCV), postglucose-load serum glucose, gestational hypertension, gestational age at birth, and birth weight were recorded in 563 participants."3.88Early pregnancy folate-cobalamin interactions and their effects on cobalamin status and hematologic variables throughout pregnancy. ( Ballesteros, M; Cavallé-Busquets, P; Colomina, JM; Fernandez-Ballart, J; Inglès-Puig, M; Murphy, MM; Ornosa-Martín, G; Salat-Batlle, J; Solé-Navais, P; Ueland, PM, 2018)
"This study aimed to investigate serum methylmalonic acid (MMA) and homocysteine levels and to assess their effects on pregnancy and neonatal outcomes."3.83A Prospective Study on Serum Methylmalonic Acid and Homocysteine in Pregnant Women. ( Cho, YY; Choi, R; Choi, S; Chung, JH; Kim, HJ; Kim, SW; Lee, SY; Lim, Y; Oh, SY, 2016)
"Plasma levels of folate, cobalamin, pyridoxal 5'-phosphate (vitamin B6), riboflavin, and the metabolic markers total homocysteine, methylmalonic acid and 3-hydro-xykynurenine were measured in pregnancy week 18 and related to reported intake of folic acid from 4 weeks prior to conception throughout week 18 in 2911 women from the Norwegian Mother and Child Cohort Study (MoBa) conducted by the Norwegian Institute of Public Health."3.79Maternal B vitamin status in pregnancy week 18 according to reported use of folic acid supplements. ( Bjørke-Monsen, AL; Magnus, P; Midttun, Ø; Nilsen, RM; Reichborn-Kjennerud, T; Roth, C; Stoltenberg, C; Susser, E; Ueland, PM; Vollset, SE, 2013)
"Hyperhomocysteinemia is a risk factor in obstetrical complications such as pre-eclampsia, 'hemolysis, elevated liver enzymes, low platelet' (HELLP)-syndrome and placental insufficiency."3.72Alteration of homocysteine catabolism in pre-eclampsia, HELLP syndrome and placental insufficiency. ( Geisel, J; Herrmann, W; Hübner, U; Koch, I; Obeid, R; Retzke, U, 2004)
"We report on a favourable pregnancy in a woman affected by mut- methylmalonic acidaemia."3.71Successful pregnancy in a woman with mut- methylmalonic acidaemia. ( Baiocco, F; Boenzi, S; Deodato, F; Dionisi-Vici, C; Rizzo, C; Sabetta, G, 2002)
"Prenatal diagnosis for combined methylmalonic aciduria and homocystinuria was performed in five at-risk pregnancies by determination of methylmalonic acid (MMA) and total homocysteine (Hcy) in amniotic fluid supernatant."3.70Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria. ( Chadefaux-Vekemans, B; Garcia, MJ; Jakobs, C; Kamoun, P; Merinero, B; Pérez-Cerdá, C; Tonetti, C; Ugarte, M; Zittoun, J, 1998)
"Methylmalonic acidaemia is an inborn error of metabolism characterized by recurrent episodes of life-threatening ketoacidosis."3.70Successful pregnancy in severe methylmalonic acidaemia. ( Desnick, RJ; Eddleman, K; Gaddipati, S; Sansaricq, C; Snyderman, SE; Wasserstein, MP, 1999)
"To determine the significance of the commonly observed fall in serum vitamin B12 levels during pregnancy, serum levels of the B12 metabolites methylmalonic acid (MMA) and homocysteine (Hcy) were measured in a group of 50 pregnant patients with subnormal serum B12 (range 45-199 pg/ml) and the results compared with those of 25 pregnant controls (serum B12(208-580) pg/ml)."3.69Biochemical indices of vitamin B12 nutrition in pregnant patients with subnormal serum vitamin B12 levels. ( Bennett, M; Bottiglieri, T; Hyland, K; McGrath, K; Metz, J, 1995)
"The role of folic acid in the primary prevention of neural tube defects (NTDs) is well established."3.69Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects. ( Adams, MJ; Cheek, JE; Haddow, JE; Henry, JP; Khoury, MJ; Knight, GJ; Scanlon, KS; Stabler, SP; Stevenson, RE; Sylvester, GC, 1995)
" We considered whether homocysteine metabolism via the enzyme methionine synthase, which requires both folate and B12, could be the critical defect in folate-related neural tube defects."3.69Homocysteine metabolism in pregnancies complicated by neural-tube defects. ( Conley, MR; Kirke, PN; Lee, YJ; McPartlin, JM; Mills, JL; Scott, JM; Weir, DG, 1995)
" Two groups of ewes were fed on a cobalt-deficient diet throughout pregnancy; one group (group A) was given the diet from the beginning of pregnancy, whilst the other (group B) received the diet for 16 weeks before mating."3.66Effects of cobalt deficiency in pregnant and post-parturient ewes and their lambs. ( Duncan, WR; Garton, GA; Morrison, ER, 1981)
"In a pregnant woman, who had given birth to a child with methylmalonic acidaemia previously, urinary methylmalonate was measured at various intervals in the second half of the pregnancy."3.66Methylmalonate excretion in a pregnancy at risk for methylmalonic acidaemia. ( Bakker, HD; Duran, M; van Gennip, AH; Wadman, SK, 1978)
"Women were immunized with pandemic influenza A (H1N1) vaccine at 26- to 28-week gestation."2.82Vitamin B12 supplementation during pregnancy and postpartum improves B12 status of both mothers and infants but vaccine response in mothers only: a randomized clinical trial in Bangladesh. ( Ahmad, SM; Ahmed, T; Ahsan, KB; Allen, LH; Hampel, D; Rahman, SM; Raqib, R; Rashid, M; Roy, A; Shahab-Ferdows, S; Siddiqua, TJ, 2016)
"Vitamin B12 deficiency is common in certain populations, such as in India, where there is also a rising prevalence of Type 2 diabetes, obesity and their complications."2.50The role of the one-carbon cycle in the developmental origins of Type 2 diabetes and obesity. ( Finer, S; Hitman, G; Saravanan, P; Yajnik, C, 2014)
"A total of 63."1.62Maternal vitamin B12 deficiency and perinatal outcomes in southern India. ( Dwarkanath, P; Finkelstein, JL; Fothergill, A; Krisher, JT; Kurpad, AV; Thomas, T, 2021)
"Pregnancy is a state of increased demand and delayed postpartum repletion of nutrients may predispose women to depression."1.62Cross-sectional association between vitamin B12 status and probable postpartum depression in Indian women. ( Bharadwaj, B; Dhiman, P; Pillai, RR; Premkumar, N; Rajendiran, S; Ranjan, VP; Wilson, AB, 2021)
"Methylmalonic aciduria is treated with a natural protein-restricted diet with adequate energy intake to sustain metabolic balance."1.62Dietary Treatment from Birth to Pregnancy in a Woman with Methylmalonic Aciduria. ( Kowalik, A; MacDonald, A; Sykut-Cegielska, J, 2021)
"Methylmalonic Acidurias (MMAs) are a group of inborn errors of metabolism (IEMs), specifically of propionate catabolism characterized by gastrointestinal and neurometabolic manifestations resulting from a deficiency in the function of methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and cobalamin metabolism."1.56A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy. ( Brindisino, P; Cicalini, I; Consalvo, A; De Laurenzi, V; Dionisi-Vici, C; Gasparroni, G; Gazzolo, D; Pieragostino, D; Rizzo, C; Rossi, C; Semeraro, D; Valentinuzzi, S; Zucchelli, M, 2020)
"Methylmalonic acid (MMA) is a sensitive indicator of B12 status."1.46South Asian Ethnicity Is Related to the Highest Risk of Vitamin B12 Deficiency in Pregnant Canadian Women. ( Green, TJ; Isman, C; Jeruszka-Bielak, M; Lamers, Y; Li, W; Schroder, TH, 2017)
"Methylmalonic acid (MMA) is a by-product of propionic acid metabolism through the vitamin B12 (cobalamin)-dependent enzyme methylmalonyl CoA mutase."1.43A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. ( Abaan, HO; Bailey-Wilson, JE; Brody, LC; Casey, M; Cropp, CD; Cunningham, C; Kim, Y; McGaughey, DM; McNulty, H; Mills, JL; Molloy, AM; O'Neill, MB; Pangilinan, F; Shane, B; Strain, JJ; Ueland, PM; Velkova, A; Ward, M; Wilson, AF, 2016)
"Presently pregnancy is no more exceptional in women with metabolic diseases."1.39Pregnancy in a methylmalonic acidemia patient with kidney transplantation: a case report. ( Bellelli, E; Carducci, C; Elli, M; Gentile, I; Labriola, D; Lubrano, R; Paoli, S; Pérez, B; Santagata, S; Ugarte, M, 2013)
"Methylmalonic aciduria is an inborn error of metabolism characterized by accumulation of methylmalonate (MMA), propionate and 2-methylcitrate (2-MCA) in body fluids."1.39Brain damage in methylmalonic aciduria: 2-methylcitrate induces cerebral ammonium accumulation and apoptosis in 3D organotypic brain cell cultures. ( Ballhausen, D; Bonafé, L; Braissant, O; Henry, H; Jafari, P; Zavadakova, P, 2013)
"Methylmalonic aciduria is a common inherited metabolic disorder."1.37Prenatal diagnosis of methylmalonic aciduria by measuring methylmalonic acid in dried amniotic fluid on filter paper using gas chromatography-mass spectrometry. ( Inoue, Y; Ohse, M, 2011)
"The occurrence of non-mosaic double trisomy is exceptional in newborns."1.35Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism. ( Alves da Silva, AF; Biselli, JM; Carvalho, VM; Eberlin, MN; Goloni-Bertollo, EM; Haddad, R; Machado, FB; Medina-Acosta, E; Pavarino-Bertelli, EC; Vannucchi, H; Zampieri, BL, 2009)
"Thereby, the underlying pernicious anemia was masked."1.35[Thromboembolic events, abortions and a sick infant--unusual presentation of a vitamin deficiency]. ( Driever, PH; Hennermann, JB; Massenkeil, G; Sturm, I; von Arnim-Baas, A, 2008)
" The pathomechanisms involved are still unknown, a contribution of toxic organic acids, in particular MMA, has been suggested."1.31Neurodegeneration in methylmalonic aciduria involves inhibition of complex II and the tricarboxylic acid cycle, and synergistically acting excitotoxicity. ( Farkas, LM; Feyh, P; Hinz, A; Hoffmann, GF; Hörster, F; Kölker, S; Mayatepek, E; Okun, JG; Sauer, S; Unsicker, K, 2002)
" The dosage of these two substances help to differenciate between both carencies, but it is not determinant of any of them and is an expensive method."1.30[Megaloblastic anemia: rapid and economical study]. ( Cicchetti, G; Marín, GH; Tentoni, J, 1997)
"Methylmalonic aciduria is a rare metabolic disorder of amino acid metabolism that is characterized by accumulation of large amounts of methylmalonic acid in the blood and urine."1.29Methylmalonic aciduria in pregnancy: a case report. ( Diss, E; Iams, J; Reed, N; Roe, C; Roe, DS, 1995)
"Methylmalonic acid was measured in cattle urine by decarboxylating it to propionate with sulfuric acid and heat and quantifying the propionate so formed by gas-liquid chromatography."1.26A technique for measurement of methylmalonic acid in cattle urine. ( Barton, EP; Elliot, JM, 1977)

Research

Studies (118)

TimeframeStudies, this research(%)All Research%
pre-199028 (23.73)18.7374
1990's19 (16.10)18.2507
2000's32 (27.12)29.6817
2010's27 (22.88)24.3611
2020's12 (10.17)2.80

Authors

AuthorsStudies
Liu, Y3
Chen, Z1
Kang, L1
He, R1
Song, J1
Shi, C1
Chen, J1
Dong, H2
Zhang, Y3
Ma, Y1
Wu, T1
Wang, Q2
Ding, Y2
Li, X1
Li, D1
Li, M1
Jin, Y2
Qin, J3
Yang, Y1
Rojas-Gómez, A1
Solé-Navais, P2
Cavallé-Busquets, P2
Ornosa-Martin, G2
Grifoll, C1
Ramos-Rodriguez, C1
Fernandez-Ballart, J2
Masana, L1
Ballesteros, M2
Ueland, PM9
Murphy, MM3
Lipari Pinto, P1
Florindo, C1
Janeiro, P1
Santos, RL1
Mexia, S1
Rocha, H1
Tavares de Almeida, I1
Vilarinho, L1
Gaspar, A1
Delgado, JA1
Pastor García, MI1
Márquez Jiménez, N1
Costa Petit, G1
Regís Perelló, A1
Robles, J1
Bauça, JM1
King, JH1
Kwan, STC1
Bae, S2
Klatt, KC1
Yan, J2
Malysheva, OV1
Jiang, X2
Roberson, MS1
Caudill, MA2
Rossi, C1
Cicalini, I1
Rizzo, C2
Zucchelli, M1
Consalvo, A1
Valentinuzzi, S1
Semeraro, D1
Gasparroni, G1
Brindisino, P1
Gazzolo, D1
Dionisi-Vici, C3
De Laurenzi, V1
Pieragostino, D1
Kowalik, A1
MacDonald, A1
Sykut-Cegielska, J1
Dhiman, P1
Pillai, RR1
Wilson, AB1
Premkumar, N1
Bharadwaj, B1
Ranjan, VP1
Rajendiran, S1
Gabriel, MC1
Rice, SM1
Sloan, JL1
Mossayebi, MH1
Venditti, CP2
Al-Kouatly, HB1
Chen, T1
Liang, L1
Zhang, H1
Ye, J1
Qiu, W1
Xiao, B1
Zhu, H1
Wang, L1
Xu, F1
Gong, Z1
Gu, X1
Han, L1
Finkelstein, JL1
Fothergill, A1
Krisher, JT1
Thomas, T2
Kurpad, AV2
Dwarkanath, P1
Zharmakhanova, G1
Syrlybayeva, L1
Kononets, V1
Nurbaulina, E1
Baikadamova, L1
Schwinger, C1
Sharma, S1
Chandyo, RK1
Hysing, M1
Kvestad, I1
Ulak, M1
Ranjitkar, S1
Shrestha, M1
Shrestha, LP1
McCann, A1
Strand, TA1
Jeruszka-Bielak, M1
Isman, C1
Schroder, TH3
Li, W1
Green, TJ1
Lamers, Y3
Salat-Batlle, J1
Inglès-Puig, M1
Colomina, JM1
Liu, YP1
Song, JQ2
Zheng, H1
Ma, YY1
Wu, TF1
Li, XY1
Li, DX1
Li, MQ1
Wang, ZX1
Yuan, Y1
Li, HX1
Yang, YL2
Huemer, M1
Diodato, D1
Martinelli, D1
Olivieri, G1
Blom, H1
Gleich, F1
Kölker, S2
Kožich, V1
Morris, AA1
Seifert, B1
Froese, DS1
Baumgartner, MR1
Martin, CA1
Baethmann, M1
Ballhausen, D2
Blasco-Alonso, J1
Boy, N1
Bueno, M1
Burgos Peláez, R1
Cerone, R1
Chabrol, B1
Chapman, KA1
Couce, ML1
Crushell, E1
Dalmau Serra, J1
Diogo, L1
Ficicioglu, C2
García Jimenez, MC1
García Silva, MT1
Gaspar, AM1
Gautschi, M1
González-Lamuño, D1
Gouveia, S1
Grünewald, S1
Hendriksz, C2
Janssen, MCH1
Jesina, P1
Koch, J1
Konstantopoulou, V1
Lavigne, C1
Lund, AM1
Martins, EG1
Meavilla Olivas, S1
Mention, K1
Mochel, F1
Mundy, H1
Murphy, E1
Paquay, S1
Pedrón-Giner, C1
Ruiz Gómez, MA1
Santra, S1
Schiff, M1
Schwartz, IV1
Scholl-Bürgi, S1
Servais, A1
Skouma, A1
Tran, C1
Vives Piñera, I1
Walter, J1
Weisfeld-Adams, J1
Sukumar, N1
Saravanan, P2
Tan, A1
Mattman, A1
Sinclair, G1
Barr, SI1
Vallance, HD1
Lubrano, R1
Bellelli, E1
Gentile, I1
Paoli, S1
Carducci, C2
Santagata, S1
Pérez, B1
Ugarte, M2
Labriola, D1
Elli, M1
Donti, TR1
Stromberger, C1
Ge, M1
Eldin, KW1
Craigen, WJ1
Graham, BH1
Finer, S1
Hitman, G1
Yajnik, C1
Scolamiero, E1
Villani, GR1
Ingenito, L1
Pecce, R1
Albano, L1
Caterino, M1
di Girolamo, MG1
Di Stefano, C1
Franzese, I1
Gallo, G1
Ruoppolo, M1
Kalay, Z1
Islek, A1
Parlak, M1
Kirecci, A1
Guney, O1
Koklu, E1
Kalay, S1
Siddiqua, TJ1
Ahmad, SM1
Ahsan, KB1
Rashid, M1
Roy, A1
Rahman, SM1
Shahab-Ferdows, S1
Hampel, D1
Ahmed, T1
Allen, LH1
Raqib, R1
West, AA1
Perry, CA1
Malysheva, O1
Stabler, SP6
Allen, RH5
Visentin, CE1
Masih, SP1
Plumptre, L1
Sohn, KJ1
Ly, A1
Lausman, AY1
Berger, H1
Croxford, R1
Kim, YI1
O'Connor, DL1
Molloy, AM2
Pangilinan, F1
Mills, JL2
Shane, B1
O'Neill, MB1
McGaughey, DM1
Velkova, A1
Abaan, HO1
McNulty, H1
Ward, M1
Strain, JJ1
Cunningham, C1
Casey, M1
Cropp, CD1
Kim, Y1
Bailey-Wilson, JE1
Wilson, AF1
Brody, LC1
Choi, R1
Choi, S1
Lim, Y1
Cho, YY1
Kim, HJ1
Kim, SW1
Chung, JH1
Oh, SY1
Lee, SY1
Sturm, I1
Hennermann, JB1
von Arnim-Baas, A1
Driever, PH1
Massenkeil, G1
Lopreato, FR1
Carvalho, FR1
Hirata, RD2
Hirata, MH2
Robi, DL1
Sampaio-Neto, LF2
Guerra-Shinohara, EM3
Thompson, MD1
Cole, DE1
Ray, JG1
Tang, H1
Hao, H2
Tang, SH1
Chen, X1
Liu, F1
Cha, QB1
Li, YQ1
Li, HJ1
Sun, L1
Yu, M1
Xiao, X1
Zhou, TH1
Vanderjagt, DJ1
Ujah, IA1
Patel, A1
Kellywood, J1
Crossey, MJ1
Obande, OS1
Glew, RH1
Biselli, JM2
Machado, FB1
Zampieri, BL2
Alves da Silva, AF1
Goloni-Bertollo, EM2
Haddad, R1
Eberlin, MN1
Vannucchi, H2
Carvalho, VM2
Medina-Acosta, E1
Pavarino-Bertelli, EC1
Pereira, PM1
Kubota, AM1
Silva, TA1
Reis, JL1
Miyashita, GS1
D'Almeida, V1
Quadros, EV1
Lai, SC1
Nakayama, Y1
Sequeira, JM1
Hannibal, L1
Wang, S1
Jacobsen, DW1
Fedosov, S1
Wright, E1
Gallagher, RC1
Anastasio, N1
Watkins, D1
Rosenblatt, DS3
Hussein, L1
Abdel Aziz, S1
Tapouzada, S1
Boehles, H1
Weber-Ferro, W1
Hertzberg, C1
Röder, H1
Timme, K1
Rossi, R1
Inoue, Y1
Ohse, M1
Carrillo-Carrasco, N1
Chandler, RJ1
Greibe, E1
Andreasen, BH1
Lildballe, DL1
Morkbak, AL1
Hvas, AM3
Nexo, E1
Cordeiro, JA1
Pavarino, EC1
Bjørke-Monsen, AL1
Roth, C1
Magnus, P1
Midttun, Ø1
Nilsen, RM1
Reichborn-Kjennerud, T1
Stoltenberg, C1
Susser, E1
Vollset, SE3
Jafari, P1
Braissant, O1
Zavadakova, P1
Henry, H1
Bonafé, L1
Samuel, TM1
Duggan, C1
Bosch, R1
Rajendran, R1
Virtanen, SM1
Srinivasan, K1
Boneh, A1
Greaves, RF1
Garra, G1
Pitt, JJ1
Deodato, F1
Boenzi, S1
Baiocco, F1
Sabetta, G1
WHITE, AM1
COX, EV1
Bjørke Monsen, AL3
Refsum, H4
Markestad, T2
Francis, PJ1
Calver, DM1
Barnfield, P1
Turner, C1
Dalton, RN1
Champion, MP1
Luo, X1
Zhang, L1
Wei, H1
Liu, W1
Wang, M1
Ning, Q1
Herrmann, W2
Hübner, U1
Koch, I1
Obeid, R2
Retzke, U1
Geisel, J1
Hasegawa, Y2
Iga, M1
Kimura, M1
Shigematsu, Y1
Yamaguchi, S2
Munz, W1
Jäger, M1
Schmidt, W1
Adeyemi, OA1
Girish, T1
Mukhopadhyay, S1
Olczak, SA1
Ahmed, Z1
Cavicchi, C1
Donati, MA1
Funghini, S1
la Marca, G1
Malvagia, S1
Ciani, F1
Poggi, GM1
Pasquini, E1
Zammarchi, E1
Morrone, A1
Campbell, CD1
Ganesh, J1
Milman, N2
Byg, KE2
Bergholt, T2
Eriksen, L2
Barbosa, PR1
Machado, AL1
Braga, RC1
Fernandez-Ballart, JD1
Schneede, J2
Arija, V1
Scott, JM2
Silf, K1
McMaster, P1
Yajnik, CS1
Deshpande, SS1
Jackson, AA1
Rao, S1
Fisher, DJ1
Bhat, DS1
Naik, SS1
Coyaji, KJ1
Joglekar, CV1
Joshi, N1
Lubree, HG1
Deshpande, VU1
Rege, SS1
Fall, CH1
Song, YZ1
Li, BX1
Xin, RL1
Zhang, T1
Zhang, CH1
Kobayashi, K1
Wang, ZN1
Zheng, XY1
Shi, CY1
Sayami, S1
Liu, P1
Yan, R1
Dong, JH1
Kleijer, WJ2
Thoomes, R1
Galjaard, H1
Wendel, U4
Fowler, B3
Fensom, AH1
Benson, PF1
Chalmers, RA1
Tracey, BM1
Watson, D1
King, GS1
Pettit, BR1
Rodeck, CH1
Jakobs, C4
Sweetman, L4
Nyhan, WL4
Dorland, L1
Duran, M2
Wadman, SK2
Zinn, AB1
Hine, DG1
Mahoney, MJ2
Tanaka, K3
Naylor, G1
Hornbeck, C1
Griffiths, J1
Mörch, L1
Brandänge, S1
Croom, WJ1
Bauman, DE1
Davis, CL1
Duncan, WR1
Morrison, ER1
Garton, GA1
Trefz, FK1
Schmidt, H1
Tauscher, B1
Depène, E1
Baumgartner, R2
Hammersen, G1
Kochen, W1
Soda, H1
Ohura, T1
Yoshida, I1
Aramaki, S1
Aoki, K1
Inokuchi, T1
Mikami, H1
Narisawa, K1
Adams, MJ1
Khoury, MJ1
Scanlon, KS1
Stevenson, RE1
Knight, GJ1
Haddow, JE1
Sylvester, GC1
Cheek, JE1
Henry, JP1
Parvy, P1
Bardet, J1
Chadefaux-Vekemans, B3
Rabier, D2
Gasquet, M1
Aupetit, J1
Kamoun, P3
Zass, R1
Leupold, D2
Fernandez, MA1
Metz, J1
McGrath, K1
Bennett, M1
Hyland, K1
Bottiglieri, T1
McPartlin, JM1
Kirke, PN1
Lee, YJ1
Conley, MR1
Weir, DG1
Diss, E1
Iams, J1
Reed, N1
Roe, DS1
Roe, C1
Rolland, MO1
Lyonnet, S1
Divry, P1
Bose, S1
Komorowski, R1
Seetharam, S1
Gilfix, B1
Seetharam, B1
Aspler, AL1
Shevell, MI1
Pletcher, BA1
Fenton, WA1
Seashore, MR1
Marín, GH1
Tentoni, J1
Cicchetti, G1
Merinero, B1
Pérez-Cerdá, C1
Garcia, MJ1
Tonetti, C1
Zittoun, J1
Norberg, B1
Wasserstein, MP1
Gaddipati, S1
Snyderman, SE1
Eddleman, K1
Desnick, RJ1
Sansaricq, C1
Pardo, J1
Peled, Y1
Bar, J1
Hod, M1
Sela, BA1
Rafael, ZB1
Orvieto, R1
Guttormsen, AB1
Solheim, E1
McMullin, MF1
Young, PB1
Bailie, KE1
Savage, GA1
Lappin, TR1
White, R1
Bondevik, GT1
Lie, RT1
Ulstein, M1
Kvåle, G1
Okun, JG1
Hörster, F1
Farkas, LM1
Feyh, P1
Hinz, A1
Sauer, S1
Hoffmann, GF1
Unsicker, K1
Mayatepek, E1
Morrow, G1
Revsin, B1
Lebowitz, J1
Britt, W1
Giles, H1
Ampola, MG1
Nakamura, E2
Kalamegham, R1
Krishnaswamy, K1
Bakker, HD1
van Gennip, AH1
Woolf, LI1
Barton, EP1
Elliot, JM1
Petersen, BJ1
Vahouny, GV1
Rosenberg, LE1
Kamoun, PP1
Chadefaux, B1
van der Meer, SB2
Spaapen, LJ2
Evans, MI2
Schulman, JD3
Fisher, GE1
Holm, J1
Ponders, L1
MacPherson, A1
Giles, L1
Sardharwalla, IB1
Donnai, P1
Clayton, JK1
Kretschmer, RE1
Bachmann, C1
Tsukahara, M1
Endo, F1
Aoki, Y1
Matsuo, K1
Kajii, T1
Royer, P1

Clinical Trials (8)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phase 1 Study of the Effect of Maternal Nutritional Status on Placental Vascular Function, Fetal Growth and Intrauterine Growth Retardation.[NCT01778205]831 participants (Actual)Observational2005-01-31Completed
Effect of Maternal Choline Intake on Maternal/Fetal Biomarkers of Choline Status[NCT01127022]82 participants (Actual)Interventional2009-01-31Completed
[NCT02244684]368 participants (Actual)Observational2010-09-30Completed
Supplementation of Vitamin B12 in Pregnancy and Postpartum on Growth and Cognitive Functioning in Early Childhood: A Randomized, Placebo Controlled Trial[NCT03071666]Phase 2/Phase 3800 participants (Actual)Interventional2017-03-27Active, not recruiting
Cobalamin Status in Young Children With Gastrointestinal Symptoms or Feeding Problems[NCT00710359]100 participants (Anticipated)Interventional2008-04-30Completed
Cobalamin Supplementation During Infancy; Effect on B-vitamin Status, Growth and Psychomotor Development[NCT00479479]107 participants (Actual)Interventional2004-12-31Completed
Cobalamin Status in Young Children With Developmental Delay and Regression[NCT00710138]100 participants (Anticipated)Interventional2008-06-30Completed
Micronutrient Status in Pregnant and Lactating Women and Their Infants[NCT03272022]272 participants (Actual)Observational2011-12-14Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

6 reviews available for methylmalonic acid and Pregnancy

ArticleYear
The role of the one-carbon cycle in the developmental origins of Type 2 diabetes and obesity.
    Diabetic medicine : a journal of the British Diabetic Association, 2014, Volume: 31, Issue:3

    Topics: Adiposity; Carbon Cycle; Diabetes Mellitus, Type 2; Environmental Exposure; Female; Fetal Developmen

2014
Vitamin B-12 and neural tube defects: the Canadian experience.
    The American journal of clinical nutrition, 2009, Volume: 89, Issue:2

    Topics: Adult; Biological Availability; Biomarkers; Canada; Female; Flour; Folic Acid; Food, Fortified; Huma

2009
Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:1

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Carrier Proteins; Child; Child, Preschool; Female;

2012
[Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].
    Klinische Wochenschrift, 1977, Jan-15, Volume: 55, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant, Newborn; Ketosis; Malonates; Methylmal

1977
The dietary treatment of inborn errors of metabolism.
    The Proceedings of the Nutrition Society, 1976, Volume: 35, Issue:1

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anemia, Megaloblastic; Child; Female; Folic Acid;

1976
In utero treatment of fetal metabolic disorders.
    Clinical obstetrics and gynecology, 1991, Volume: 34, Issue:2

    Topics: Adrenal Hyperplasia, Congenital; Female; Fetal Diseases; Humans; Metabolism, Inborn Errors; Methylma

1991

Trials

6 trials available for methylmalonic acid and Pregnancy

ArticleYear
Maternal choline supplementation alters vitamin B-12 status in human and murine pregnancy.
    The Journal of nutritional biochemistry, 2019, Volume: 72

    Topics: Adult; Animals; Betaine-Homocysteine S-Methyltransferase; Choline; Choline Dehydrogenase; Dietary Su

2019
Cobalamin and folate status in women during early pregnancy in Bhaktapur, Nepal.
    Journal of nutritional science, 2021, Volume: 10

    Topics: Female; Folic Acid; Homocysteine; Humans; Methylmalonic Acid; Nepal; Pregnancy; Vitamin B 12; Vitami

2021
Vitamin B12 supplementation during pregnancy and postpartum improves B12 status of both mothers and infants but vaccine response in mothers only: a randomized clinical trial in Bangladesh.
    European journal of nutrition, 2016, Volume: 55, Issue:1

    Topics: Adolescent; Adult; Bangladesh; Biomarkers; C-Reactive Protein; Dietary Supplements; Dose-Response Re

2016
Vitamin B-12 Status Differs among Pregnant, Lactating, and Control Women with Equivalent Nutrient Intakes.
    The Journal of nutrition, 2015, Volume: 145, Issue:7

    Topics: Adult; Biomarkers; Breast Feeding; Choline; Dietary Supplements; Dose-Response Relationship, Drug; D

2015
Biochemical indexes of the B vitamins in cord serum are predicted by maternal B vitamin status.
    The American journal of clinical nutrition, 2005, Volume: 82, Issue:1

    Topics: Adult; Female; Fetal Blood; Gestational Age; Homocysteine; Humans; Infant, Newborn; Male; Maternal-F

2005
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001
Determinants of cobalamin status in newborns.
    Pediatrics, 2001, Volume: 108, Issue:3

    Topics: Adult; Biomarkers; Female; Homocysteine; Humans; Infant, Newborn; Logistic Models; Maternal-Fetal Ex

2001

Other Studies

106 other studies available for methylmalonic acid and Pregnancy

ArticleYear
Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduria.
    PloS one, 2022, Volume: 17, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Child; Female; Humans; Methylmalonic Acid; Pre

2022
Pregnancy homocysteine and cobalamin status predict childhood metabolic health in the offspring.
    Pediatric research, 2023, Volume: 93, Issue:3

    Topics: Birth Weight; Child; Female; Folic Acid; Homocysteine; Humans; Male; Methylmalonic Acid; Pregnancy;

2023
Acquired Vitamin B12 Deficiency in Newborns: Positive Impact on Newborn Health through Early Detection.
    Nutrients, 2022, Oct-20, Volume: 14, Issue:20

    Topics: Biomarkers; Early Diagnosis; Female; Homocysteine; Humans; Hydroxocobalamin; Infant; Infant Health;

2022
Functional vitamin B12 deficiency: Improving methylmalonic acid reference intervals in urine.
    Clinica chimica acta; international journal of clinical chemistry, 2023, Apr-01, Volume: 544

    Topics: Biomarkers; Female; Humans; Methylmalonic Acid; Pregnancy; Prospective Studies; Vitamin B 12; Vitami

2023
A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy.
    International journal of environmental research and public health, 2020, 05-20, Volume: 17, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Liquid; Female; Humans; Infant, Newborn; Malnu

2020
Dietary Treatment from Birth to Pregnancy in a Woman with Methylmalonic Aciduria.
    Medicina (Kaunas, Lithuania), 2021, Feb-02, Volume: 57, Issue:2

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Diet; Dietary Supplements; Female; Humans;

2021
Cross-sectional association between vitamin B12 status and probable postpartum depression in Indian women.
    BMC pregnancy and childbirth, 2021, Feb-17, Volume: 21, Issue:1

    Topics: Adolescent; Adult; Cesarean Section; Cross-Sectional Studies; Depression, Postpartum; Diet; Female;

2021
Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria.
    Molecular genetics & genomic medicine, 2021, Volume: 9, Issue:4

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amniocentesis; Carboxy-Lyases; Coenzyme A Ligases; Fema

2021
Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type.
    Orphanet journal of rare diseases, 2021, 03-10, Volume: 16, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Homocysteine; Homocystinuria; Humans;

2021
Maternal vitamin B12 deficiency and perinatal outcomes in southern India.
    PloS one, 2021, Volume: 16, Issue:4

    Topics: Adult; Biomarkers; Cohort Studies; Female; Folic Acid; Humans; India; Infant, Newborn; Maternal Nutr

2021
[MOLECULAR-GENETIC ASPECTS OF METHYLMALONIC ACIDURIA DEVELOPMENT (REVIEW)].
    Georgian medical news, 2021, Issue:313

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Female; Humans; Methylmalonic Acid; Methylmalonyl-CoA M

2021
South Asian Ethnicity Is Related to the Highest Risk of Vitamin B12 Deficiency in Pregnant Canadian Women.
    Nutrients, 2017, Mar-23, Volume: 9, Issue:4

    Topics: Adolescent; Adult; Asia; Biomarkers; Canada; Ethnicity; Female; Gestational Age; Humans; India; Meth

2017
Early pregnancy folate-cobalamin interactions and their effects on cobalamin status and hematologic variables throughout pregnancy.
    The American journal of clinical nutrition, 2018, 02-01, Volume: 107, Issue:2

    Topics: Adult; Anemia, Iron-Deficiency; Body Mass Index; Dietary Supplements; Female; Folic Acid; Homocystei

2018
[Heterogeneous phenotypes, genotypes, treatment and prevention of 1 003 patients with methylmalonic acidemia in the mainland of China].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2018, Jun-02, Volume: 56, Issue:6

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Carrier Proteins; Child; Child, Preschool;

2018
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:2

    Topics: Adolescent; Adult; Age of Onset; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cros

2019
Investigating vitamin B12 deficiency.
    BMJ (Clinical research ed.), 2019, May-10, Volume: 365

    Topics: Adult; Aged; Biomarkers; Female; Folic Acid; Health Surveys; Homocysteine; Humans; Infant; Malabsorp

2019
Reference intervals for serum total vitamin B12 and holotranscobalamin concentrations and their change points with methylmalonic acid concentration to assess vitamin B12 status during early and mid-pregnancy.
    Clinical chemistry and laboratory medicine, 2019, Oct-25, Volume: 57, Issue:11

    Topics: Adult; Biomarkers; Female; Humans; Methylmalonic Acid; Pregnancy; Reference Values; Transcobalamins;

2019
Pregnancy in a methylmalonic acidemia patient with kidney transplantation: a case report.
    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2013, Volume: 13, Issue:7

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Follow-Up Studies; Glomerular F

2013
Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletion.
    Disease models & mechanisms, 2014, Volume: 7, Issue:2

    Topics: Alleles; Animals; Calcification, Physiologic; DNA, Mitochondrial; Embryo Loss; Embryo, Mammalian; Em

2014
Maternal vitamin B12 deficiency detected in expanded newborn screening.
    Clinical biochemistry, 2014, Volume: 47, Issue:18

    Topics: Carnitine; Female; Folic Acid; Homocysteine; Humans; Infant, Newborn; Methylmalonic Acid; Neonatal S

2014
Reliable and powerful laboratory markers of cobalamin deficiency in the newborn: plasma and urinary methylmalonic acid.
    The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2016, Volume: 29, Issue:1

    Topics: Adult; Biomarkers; Cohort Studies; Female; Homocysteine; Humans; Infant, Newborn; Methylmalonic Acid

2016
Low Serum Vitamin B-12 Concentrations Are Prevalent in a Cohort of Pregnant Canadian Women.
    The Journal of nutrition, 2016, Volume: 146, Issue:5

    Topics: Adult; Canada; Diet; Dietary Supplements; DNA Methylation; Female; Fetal Blood; Fetus; Folic Acid; H

2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin.
    American journal of human genetics, 2016, May-05, Volume: 98, Issue:5

    Topics: Abnormalities, Multiple; Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Case-Control

2016
A Prospective Study on Serum Methylmalonic Acid and Homocysteine in Pregnant Women.
    Nutrients, 2016, Dec-08, Volume: 8, Issue:12

    Topics: Adult; Female; Homocysteine; Humans; Infant, Newborn; Methylmalonic Acid; Middle Aged; Pregnancy; Pr

2016
[Thromboembolic events, abortions and a sick infant--unusual presentation of a vitamin deficiency].
    Der Internist, 2008, Volume: 49, Issue:12

    Topics: Abortion, Habitual; Adult; Anemia, Pernicious; Autoimmune Diseases; Breast Feeding; Diagnosis, Diffe

2008
Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates.
    Clinica chimica acta; international journal of clinical chemistry, 2008, Volume: 398, Issue:1-2

    Topics: Adult; Brazil; DNA; Embryonic Development; Ethnicity; Female; Folic Acid; Glutamate Carboxypeptidase

2008
[Mutation analysis of the MMACHC gene in a pedigree with methylmalonic aciduria].
    Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2009, Volume: 26, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Animals; Base Sequence; Carrier Proteins;

2009
Subclinical vitamin B12 deficiency in pregnant women attending an antenatal clinic in Nigeria.
    Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology, 2009, Volume: 29, Issue:4

    Topics: Adult; Ambulatory Care Facilities; Female; Folic Acid; Hemoglobins; Homocysteine; Humans; Methylmalo

2009
Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Genetic counseling (Geneva, Switzerland), 2009, Volume: 20, Issue:3

    Topics: Adolescent; Alleles; Aneuploidy; Brazil; Chromosomes, Human, X; Chromosomes, Human, Y; DNA Mutationa

2009
Increased MMA concentration and body mass index are associated with spontaneous abortion in Brazilian women: a pilot study.
    Clinica chimica acta; international journal of clinical chemistry, 2010, Volume: 411, Issue:5-6

    Topics: Abortion, Spontaneous; Adult; Alleles; Body Mass Index; Brazil; DNA Mutational Analysis; Female; Gen

2010
Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B(12).
    Human mutation, 2010, Volume: 31, Issue:8

    Topics: Amino Acid Sequence; Antigens, CD; Base Sequence; Cells, Cultured; DNA Mutational Analysis; Female;

2010
Serum vitamin B(12) concentrations among mothers and newborns and follow-up study to assess implication on the growth velocity and the urinary methylmalonic acid excretion.
    International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 2009, Volume: 79, Issue:5-6

    Topics: Adolescent; Adult; Birth Weight; Body Weight; Child Development; Female; Humans; Infant, Newborn; Li

2009
Intact recovery from early 'acquired methylmalonic aciduria' secondary to maternal atrophic gastritis.
    Acta paediatrica (Oslo, Norway : 1992), 2011, Volume: 100, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Dietary Supplements; Female; Gastritis, Atrophic; Humans; Infa

2011
Prenatal diagnosis of methylmalonic aciduria by measuring methylmalonic acid in dried amniotic fluid on filter paper using gas chromatography-mass spectrometry.
    Analytical and bioanalytical chemistry, 2011, Volume: 400, Issue:7

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Gas Chromatography-Mass Spectrometry;

2011
Uptake of cobalamin and markers of cobalamin status: a longitudinal study of healthy pregnant women.
    Clinical chemistry and laboratory medicine, 2011, Volume: 49, Issue:11

    Topics: Adult; Biomarkers; Denmark; Female; Homocysteine; Humans; Longitudinal Studies; Methylmalonic Acid;

2011
Maternal risk for Down syndrome is modulated by genes involved in folate metabolism.
    Disease markers, 2012, Volume: 32, Issue:2

    Topics: Adult; Betaine-Homocysteine S-Methyltransferase; Biosynthetic Pathways; Case-Control Studies; Down S

2012
Maternal B vitamin status in pregnancy week 18 according to reported use of folic acid supplements.
    Molecular nutrition & food research, 2013, Volume: 57, Issue:4

    Topics: Adult; Biomarkers; Dietary Supplements; Fatty Acids, Omega-3; Female; Folic Acid; Homocysteine; Huma

2013
Brain damage in methylmalonic aciduria: 2-methylcitrate induces cerebral ammonium accumulation and apoptosis in 3D organotypic brain cell cultures.
    Orphanet journal of rare diseases, 2013, Jan-08, Volume: 8

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Apoptosis; Blotting, Western; Brain; Caspase 3; Cells

2013
Vitamin B(12) intake and status in early pregnancy among urban South Indian women.
    Annals of nutrition & metabolism, 2013, Volume: 62, Issue:2

    Topics: Adolescent; Adult; Anthropometry; Cross-Sectional Studies; Diet; Dietary Supplements; Erythrocytes;

2013
Metabolic treatment of pregnancy and postdelivery period in a patient with cobalamin A disease.
    American journal of obstetrics and gynecology, 2002, Volume: 187, Issue:1

    Topics: Cobamides; Female; Humans; Hydroxocobalamin; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnanc

2002
Successful pregnancy in a woman with mut- methylmalonic acidaemia.
    Journal of inherited metabolic disease, 2002, Volume: 25, Issue:2

    Topics: Adult; Carnitine; Female; Humans; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnancy; Pregnanc

2002
METHYLMALONIC ACID EXCRETION AND VITAMIN B12 DEFICIENCY IN THE HUMAN.
    Annals of the New York Academy of Sciences, 1964, Apr-24, Volume: 112

    Topics: Anemia; Anemia, Macrocytic; Anemia, Pernicious; Carcinoma; Celiac Disease; Chromatography; Crohn Dis

1964
Hematological parameters and cobalamin status in infants born to smoking mothers.
    Biology of the neonate, 2004, Volume: 85, Issue:4

    Topics: Adult; Birth Weight; Erythrocyte Count; Female; Folic Acid; Gestational Age; Hemoglobins; Homocystei

2004
An infant with methylmalonic aciduria and homocystinuria (cblC) presenting with retinal haemorrhages and subdural haematoma mimicking non-accidental injury.
    European journal of pediatrics, 2004, Volume: 163, Issue:7

    Topics: Child Abuse; Diagnosis, Differential; Female; Hematoma; Hematoma, Subdural; Homocystinuria; Humans;

2004
Methylmalonic acid in amniotic fluid and maternal urine as a marker for neural tube defects.
    Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2004, Volume: 24, Issue:2

    Topics: Adult; Amniotic Fluid; Biomarkers; Female; Folic Acid; Humans; Methylmalonic Acid; Neural Tube Defec

2004
Alteration of homocysteine catabolism in pre-eclampsia, HELLP syndrome and placental insufficiency.
    Clinical chemistry and laboratory medicine, 2004, Volume: 42, Issue:10

    Topics: Cystathionine; Cystatin C; Cystatins; Female; Folic Acid; HELLP Syndrome; Homocysteine; Humans; Hype

2004
Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005, Aug-25, Volume: 823, Issue:1

    Topics: Amniotic Fluid; Carboxylic Acids; Carnitine; Female; Fetal Diseases; Gas Chromatography-Mass Spectro

2005
Methylmalonic acidaemia: a rare metabolic disorder in pregnancy.
    Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology, 2004, Volume: 24, Issue:8

    Topics: Adult; Cesarean Section; Female; Humans; Infant, Newborn; Infant, Premature; Metabolism, Inborn Erro

2004
Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduria.
    Clinical genetics, 2006, Volume: 69, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Base Sequence; DNA Mutational Analysis; Family Health; Female;

2006
Two newborns with nutritional vitamin B12 deficiency: challenges in newborn screening for vitamin B12 deficiency.
    Haematologica, 2005, Volume: 90, Issue:12 Suppl

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Anemia, Pernicious; Autoimmune Diseases; Biomarkers; Carnitine;

2005
Cobalamin status during normal pregnancy and postpartum: a longitudinal study comprising 406 Danish women.
    European journal of haematology, 2006, Volume: 76, Issue:6

    Topics: Adult; Cohort Studies; Denmark; Female; Follow-Up Studies; Hemoglobins; Homocysteine; Humans; Infant

2006
Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women.
    European journal of clinical nutrition, 2008, Volume: 62, Issue:8

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Adult; Alleles; Analysis of V

2008
Reference intervals for haematological variables during normal pregnancy and postpartum in 434 healthy Danish women.
    European journal of haematology, 2007, Volume: 79, Issue:1

    Topics: Creatinine; Denmark; Female; Ferritins; Folic Acid; Hematologic Tests; Homocysteine; Humans; Methylm

2007
Longitudinal study of the effect of pregnancy on maternal and fetal cobalamin status in healthy women and their offspring.
    The Journal of nutrition, 2007, Volume: 137, Issue:8

    Topics: Adult; Female; Fetus; Health; Humans; Longitudinal Studies; Maternal Nutritional Physiological Pheno

2007
Methylmalonic acidaemia in a 7-month-old following maternal highly active antiretroviral therapy during pregnancy.
    AIDS (London, England), 2007, Aug-20, Volume: 21, Issue:13

    Topics: Amino Acid Metabolism, Inborn Errors; Anti-HIV Agents; Antiretroviral Therapy, Highly Active; Female

2007
Vitamin B12 and folate concentrations during pregnancy and insulin resistance in the offspring: the Pune Maternal Nutrition Study.
    Diabetologia, 2008, Volume: 51, Issue:1

    Topics: Adipose Tissue; Anthropometry; Body Composition; Body Mass Index; Child; Female; Folic Acid; Homocys

2008
Selective screening for inborn errors of metabolism and secondary methylmalonic aciduria in pregnancy at high risk district of neural tube defects: a human metabolome study by GC-MS in China.
    Clinical biochemistry, 2008, Volume: 41, Issue:7-8

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; China; Female; Gas

2008
Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid.
    Chinese medical journal, 2008, Feb-05, Volume: 121, Issue:3

    Topics: Amniotic Fluid; Carnitine; Citrates; Female; Gas Chromatography-Mass Spectrometry; Homocysteine; Hum

2008
First-trimester (chorion biopsy) diagnosis of citrullinaemia and methylmalonicaciduria.
    Lancet (London, England), 1984, Dec-08, Volume: 2, Issue:8415

    Topics: Amino Acid Metabolism, Inborn Errors; Chorionic Villi; Citrulline; Female; Humans; Malonates; Methyl

1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria.
    Journal of inherited metabolic disease, 1984, Volume: 7 Suppl 2

    Topics: Amniotic Fluid; Carboxy-Lyases; Female; Humans; Malonates; Methylmalonic Acid; Methylmalonyl-CoA Dec

1984
Hydroxy acid metabolites of branched-chain amino acids in amniotic fluid.
    Clinica chimica acta; international journal of clinical chemistry, 1984, Jul-16, Volume: 140, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Amniotic Fluid; Caproates; Female

1984
Identification of methyl-branched chain dicarboxylic acids in amniotic fluid and urine in propionic and methylmalonic acidemia.
    Pediatric research, 1984, Volume: 18, Issue:11

    Topics: Amniotic Fluid; Chromatography, Gas; Dicarboxylic Acids; Female; Humans; Malonates; Mass Spectrometr

1984
The stable isotope dilution method for measurement of methylmalonic acid: a highly accurate approach to the prenatal diagnosis of methylmalonic acidemia.
    Pediatric research, 1982, Volume: 16, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Gas Chromatography-Mass Spectrometry;

1982
Isotope dilution analysis of methylcitric acid in amniotic fluid for the prenatal diagnosis of propionic and methylmalonic acidemia.
    Clinica chimica acta; international journal of clinical chemistry, 1980, Nov-06, Volume: 107, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Chromatography, Liquid; Citrates; Female; Gas

1980
Methylmalonic acid in low-fat milk syndrome.
    Journal of dairy science, 1981, Volume: 64, Issue:4

    Topics: Acetates; Animal Feed; Animals; Cattle; Cattle Diseases; Fatty Acids; Female; Lactation; Malonates;

1981
Effects of cobalt deficiency in pregnant and post-parturient ewes and their lambs.
    The British journal of nutrition, 1981, Volume: 46, Issue:2

    Topics: Adipose Tissue; Animals; Animals, Newborn; Cobalt; Female; Lipid Metabolism; Liver; Methylmalonic Ac

1981
Improved prenatal diagnosis of methylmalonic acidemia: mass fragmentography of methylmalonic acid in amniotic fluid and maternal urine.
    European journal of pediatrics, 1981, Volume: 137, Issue:3

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Humans; Malonates; Methylmaloni

1981
Prenatal diagnosis and therapy for a patient with vitamin B12-responsive methylmalonic acidaemia.
    Journal of inherited metabolic disease, 1995, Volume: 18, Issue:3

    Topics: Female; Fetal Diseases; Humans; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnancy; Prenatal D

1995
Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects.
    Teratology, 1995, Volume: 51, Issue:5

    Topics: Adult; Case-Control Studies; Female; Folic Acid; Gas Chromatography-Mass Spectrometry; Humans; Methy

1995
Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduria.
    Clinical chemistry, 1995, Volume: 41, Issue:11

    Topics: Amino Acids; Amniocentesis; Amniotic Fluid; Female; Gestational Age; Homocystinuria; Humans; Methylm

1995
Evaluation of prenatal treatment in newborns with cobalamin-responsive methylmalonic acidaemia.
    Journal of inherited metabolic disease, 1995, Volume: 18, Issue:1

    Topics: Adipose Tissue; Fatty Acids; Female; Humans; Infant, Newborn; Metabolism, Inborn Errors; Methylmalon

1995
Biochemical indices of vitamin B12 nutrition in pregnant patients with subnormal serum vitamin B12 levels.
    American journal of hematology, 1995, Volume: 48, Issue:4

    Topics: Female; Homocysteine; Humans; Methylmalonic Acid; Nutritional Status; Pregnancy; Pregnancy Complicat

1995
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
    Lancet (London, England), 1995, Jan-21, Volume: 345, Issue:8943

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Analysis of Variance; Female; Folic Acid;

1995
Methylmalonic aciduria in pregnancy: a case report.
    American journal of obstetrics and gynecology, 1995, Volume: 172, Issue:3

    Topics: Adult; Female; Humans; Infant, Newborn; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnancy; Pr

1995
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)
    Prenatal diagnosis, 1994, Volume: 14, Issue:5

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Cobamides; Female; Homocystinuria; Humans

1994
In vitro and in vivo inactivation of transcobalamin II receptor by its antiserum.
    The Journal of biological chemistry, 1996, Feb-23, Volume: 271, Issue:8

    Topics: Animals; Antibodies; Cell Line; Cell Membrane; Cobalt Radioisotopes; Female; Homocysteine; Humans; I

1996
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).
    Journal of inherited metabolic disease, 1997, Volume: 20, Issue:4

    Topics: Adolescent; Age of Onset; Amino Acid Metabolism, Inborn Errors; Cause of Death; Child; Child, Presch

1997
[Megaloblastic anemia: rapid and economical study].
    Sangre, 1997, Volume: 42, Issue:3

    Topics: Adolescent; Adult; Algorithms; Anemia, Megaloblastic; Cost Control; Diagnosis, Differential; Diagnos

1997
Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria.
    Prenatal diagnosis, 1998, Volume: 18, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Amniotic Fluid; Cells, Cultured; Chorion; Chori

1998
Turn of tide for oral vitamin B12 treatment.
    Journal of internal medicine, 1999, Volume: 246, Issue:3

    Topics: Administration, Oral; Aged; Biological Availability; Biomarkers; England; Female; Homocysteine; Huma

1999
Successful pregnancy in severe methylmalonic acidaemia.
    Journal of inherited metabolic disease, 1999, Volume: 22, Issue:7

    Topics: Acidosis; Adult; Female; Humans; Hydroxocobalamin; Infant, Newborn; Male; Metabolism, Inborn Errors;

1999
Evaluation of low serum vitamin B(12) in the non-anaemic pregnant patient.
    Human reproduction (Oxford, England), 2000, Volume: 15, Issue:1

    Topics: Adult; Erythrocyte Indices; Female; Gestational Age; Homocysteine; Humans; Methylmalonic Acid; Parit

2000
Homocysteine and methylmalonic acid as indicators of folate and vitamin B12 deficiency in pregnancy.
    Clinical and laboratory haematology, 2001, Volume: 23, Issue:3

    Topics: Adult; Biomarkers; Female; Folic Acid Deficiency; Homocysteine; Humans; Methylmalonic Acid; Pregnanc

2001
Homocysteine and methylmalonic acid levels in pregnant Nepali women. Should cobalamin supplementation be considered?
    European journal of clinical nutrition, 2001, Volume: 55, Issue:10

    Topics: Adolescent; Adult; Biomarkers; Cross-Sectional Studies; Dietary Supplements; Female; Folic Acid; Fol

2001
Total homocysteine is making its way into pediatric laboratory diagnostics.
    European journal of clinical investigation, 2001, Volume: 31, Issue:11

    Topics: Adult; Avitaminosis; Child; Diagnosis, Differential; Female; Folic Acid; Folic Acid Deficiency; HIV

2001
Neurodegeneration in methylmalonic aciduria involves inhibition of complex II and the tricarboxylic acid cycle, and synergistically acting excitotoxicity.
    The Journal of biological chemistry, 2002, Apr-26, Volume: 277, Issue:17

    Topics: Animals; Cells, Cultured; Citrates; Citric Acid Cycle; Corpus Striatum; Electron Transport Complex I

2002
Detection of errors in methylmalonyl-CoA metabolism by using amniotic fluid.
    Clinical chemistry, 1977, Volume: 23, Issue:5

    Topics: Amniotic Fluid; Cells, Cultured; Coenzyme A; False Positive Reactions; Female; Humans; Malonates; Me

1977
Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemia.
    The New England journal of medicine, 1975, Aug-14, Volume: 293, Issue:7

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Cobamides; Female; Fetal Diseases; Gestational

1975
Functional significance of low serum vitamin B12 levels in pregnancy.
    International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 1977, Volume: 47, Issue:1

    Topics: Biological Assay; Female; Hematocrit; Hemoglobins; Humans; Methylmalonic Acid; Pregnancy; Pregnancy

1977
Methylmalonate excretion in a pregnancy at risk for methylmalonic acidaemia.
    Clinica chimica acta; international journal of clinical chemistry, 1978, Jun-15, Volume: 86, Issue:3

    Topics: Female; Humans; Infant, Newborn; Male; Malonates; Metabolism, Inborn Errors; Methylmalonic Acid; Pre

1978
A technique for measurement of methylmalonic acid in cattle urine.
    Journal of dairy science, 1977, Volume: 60, Issue:11

    Topics: Animals; Cattle; Female; Lactation; Malonates; Methylmalonic Acid; Pregnancy; Propionates

1977
Editorial: Prenatal treatment of methylmalonic acidemia.
    The New England journal of medicine, 1975, Aug-14, Volume: 293, Issue:7

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Female; Fetal Diseases; Humans; Infant, Newborn

1975
Cardiac structure and function in vitamin B-12-deprived rats.
    The Journal of nutrition, 1975, Volume: 105, Issue:12

    Topics: Animals; Fatty Acids; Female; Maternal-Fetal Exchange; Methylmalonic Acid; Mitochondria, Muscle; Myo

1975
Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: use in prenatal diagnosis of methylmalonic acidemia and in studies of isovaleric acidemia.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Apr-15, Volume: 68, Issue:2

    Topics: Adult; Child; Chromatography, Gas; Colorimetry; Dicarboxylic Acids; Evaluation Studies as Topic; Fem

1976
Eleventh week amniocentesis for prenatal diagnosis of some metabolic diseases.
    Prenatal diagnosis, 1991, Volume: 11, Issue:9

    Topics: Amniocentesis; Amniotic Fluid; Argininosuccinic Acid; Chorionic Villi Sampling; Citrulline; Female;

1991
Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.
    Pediatric research, 1991, Volume: 29, Issue:4 Pt 1

    Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Fatty Acids; Female; Fetus; Humans; Infant, N

1991
Effect of cobalt deficiency in the pregnant ewe on reproductive performance and lamb viability.
    Research in veterinary science, 1991, Volume: 50, Issue:3

    Topics: Animals; Body Weight; Cobalt; Colostrum; Female; Fetal Death; Immunoglobulin G; Methylmalonic Acid;

1991
Prenatal treatment of a patient with vitamin B12-responsive methylmalonic acidemia.
    The Journal of pediatrics, 1990, Volume: 117, Issue:6

    Topics: Acidosis; Administration, Oral; Female; Humans; Metabolism, Inborn Errors; Methylmalonic Acid; Pregn

1990
Prenatal diagnosis of propionic and methylmalonic acidaemia by stable isotope dilution analysis of amniotic fluid.
    Journal of inherited metabolic disease, 1989, Volume: 12 Suppl 2

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Citrates; Female; Gas Chromatography-Mass Spect

1989
Duration of effective benefit from administration of graded oral doses of cobalt to sheep.
    The Veterinary record, 1989, Dec-09, Volume: 125, Issue:24

    Topics: Animals; Benzimidazoles; Cobalt; Drug Administration Schedule; Female; Fenbendazole; Lactation; Meth

1989
First trimester diagnosis of methylmalonic aciduria.
    Prenatal diagnosis, 1988, Volume: 8, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Chorionic Villi; Female; Humans; Malonates; Methylmalonic Acid

1988
Methylcitric acid determination in amniotic fluid by electron-impact mass fragmentography.
    Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 1988, Volume: 26, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Citrates; Female; Gas Chromatography-Mass Spec

1988
Familial supernumerary non-satellited microchromosome.
    Clinical genetics, 1986, Volume: 30, Issue:3

    Topics: Adult; Chromosome Aberrations; Chromosome Banding; Female; Genetic Markers; Humans; Male; Metabolism

1986
Biochemical fetal therapy.
    Clinical obstetrics and gynecology, 1986, Volume: 29, Issue:3

    Topics: Adrenal Hyperplasia, Congenital; Adult; Arrhythmias, Cardiac; Copper; Female; Fetal Diseases; Galact

1986
Prenatal treatment of biochemical disorders.
    Seminars in perinatology, 1985, Volume: 9, Issue:2

    Topics: Adrenal Hyperplasia, Congenital; Female; Fetal Diseases; Galactosemias; Humans; Metabolism, Inborn E

1985
Hyperuricemia in children, with the exception of the Lesch-Nyhan syndrome.
    Advances in nephrology from the Necker Hospital, 1974, Volume: 3

    Topics: Acidosis; Acute Disease; Acute Kidney Injury; Adult; Child; Child, Preschool; Chronic Disease; Femal

1974