glycine has been researched along with Acidosis in 94 studies
Acidosis: A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Metaflumizone shares a similar chemical structure to indoxacarb, which is known to be a cause of methemoglobinemia." | 7.80 | Methemoglobinemia associated with metaflumizone poisoning. ( Choi, KH; Oh, JS, 2014) |
| " Either glycine (2 mM) or extracellular fluid acidosis (pH 7." | 7.68 | Acute phosphate depletion and in vitro rat proximal tubule injury: protection by glycine and acidosis. ( Almeida, AR; Bunnachak, D; Burke, TJ; Chaimovitz, C; Hammond, WS; Schrier, RW; Wetzels, JF, 1992) |
| "Strychnine poisoning results in a predictable and treatable sequence of events involving blockade of the inhibitory neurotransmitter, extensor muscle spasms, seizures, and respiratory paralysis." | 7.66 | Strychnine poisoning. Recovery from profound lactic acidosis, hyperthermia, and rhabdomyolysis. ( Boyd, RE; Brennan, PT; Deng, JF; Rochester, DF; Spyker, DA, 1983) |
| "Ingestion of glyphosate-surfactant herbicides (GlySH) can result in acute kidney injury, electrolyte abnormalities, acidosis, cardiovascular collapse, and death." | 3.80 | Hemodialysis clearance of glyphosate following a life-threatening ingestion of glyphosate-surfactant herbicide. ( Allan, MJ; Garlich, FM; Goldfarb, DS; Goldman, M; Goldstein, DA; Hoffman, RS; Nelson, LS; Pepe, J, 2014) |
| "Metaflumizone shares a similar chemical structure to indoxacarb, which is known to be a cause of methemoglobinemia." | 3.80 | Methemoglobinemia associated with metaflumizone poisoning. ( Choi, KH; Oh, JS, 2014) |
| " Biochemically, beta-ketothiolase deficiency is characterized by intermittent ketoacidosis and urinary excretion of 2-methyl-acetoacetate (MAA), 2-methyl-3-hydroxybutyrate (MHB) and tiglylglycine (TG), whereas in MHBD deficiency only MHB and tiglylglycine accumulate." | 3.73 | Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats. ( da C Ferreira, G; Dalcin, KB; de Assis, DR; Filho, CS; Latini, A; Leipnitz, G; Maria, RC; Perry, ML; Ribeiro, CA; Rosa, RB; Schuck, PF; Wajner, M; Wannmacher, CM; Wyse, AT, 2005) |
| " Either glycine (2 mM) or extracellular fluid acidosis (pH 7." | 3.68 | Acute phosphate depletion and in vitro rat proximal tubule injury: protection by glycine and acidosis. ( Almeida, AR; Bunnachak, D; Burke, TJ; Chaimovitz, C; Hammond, WS; Schrier, RW; Wetzels, JF, 1992) |
| "A child with a history of episodes of metabolic acidosis was found to excrete 3-hydroxyisovaleric acid and 3-methylcrotonylglycine." | 3.66 | A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria. ( Bartlett, K; Leonard, JV; Ng, H, 1980) |
| "Strychnine poisoning results in a predictable and treatable sequence of events involving blockade of the inhibitory neurotransmitter, extensor muscle spasms, seizures, and respiratory paralysis." | 3.66 | Strychnine poisoning. Recovery from profound lactic acidosis, hyperthermia, and rhabdomyolysis. ( Boyd, RE; Brennan, PT; Deng, JF; Rochester, DF; Spyker, DA, 1983) |
| "The tendency towards metabolic acidosis developing during simple infections lead to the detection of hyperglycinemia which was shown to be caused by the rare inborn error of metabolism, which was shown to be a methylmalonic acidemia, in identical twins." | 3.66 | [Vitamin-B12-dependent methylmalonic acidemia in twins]. ( Hansen, HG; Heuer, R; Karsten, J; Kneer, J; Wulff, UC, 1983) |
| " The patients suffered from distinct variants of maple syrup urine disease, propionic acidaemia, methylmalonic acidaemia, lactic acidosis and hyperglycinuria." | 3.66 | [Human fibroblast bank for studying amino acid disorders and organic acidemias]. ( del Valle, JA; Merinero, B; Pérez-Cerdá, C; Ugarte, M, 1982) |
| "A patient presenting with severe metabolic acidosis accompanied by hyperglycinemia, hyperuricemia, hypoglycemia and hypertammonemia is described." | 3.66 | Methylmalonic acidemia. ( Akaboshi, I; Hattori, S; Matsuda, I; Nagata, N; Oka, Y; Shinozuka, S; Terashima, T; Yamamoto, J, 1978) |
| "Chronic low-grade metabolic acidosis is now a common phenomenon in the Western world." | 1.91 | Dietary Acid Load Correlates with Serum Amino Acid Concentrations after a Four-Week Intervention with Vegan vs. Meat-Rich Diets: A Secondary Data Analysis. ( Hannibal, L; Herter, J; Huber, R; Lederer, AK; Ronco, AL; Storz, MA, 2023) |
| "Carnitine conjugates were however detected." | 1.29 | The detection of 3-methylglutarylcarnitine and a new dicarboxylic conjugate, 3-methylglutaconylcarnitine, in 3-methylglutaconic aciduria. ( de Wet, WJ; Erasmus, E; Gibson, KM; Jooste, S; Mienie, LJ, 1994) |
| "[15N]Glycine was infused into fed, fasted or acidotic humans." | 1.26 | [15N]Glycine metabolism in normal man: the metabolic alpha-amino-nitrogen pool. ( Golden, MH; Jackson, AA, 1980) |
| "However, ketonuria was not a consistent part of his clinical picture, and he had at least two episodes of acute overwhelming illness, the latter one fatal, in which ketones were never found in the urine." | 1.25 | Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis. ( Ando, T; Kilroy, A; Nyhan, WL; Sweetman, L; Wadlington, WB, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 68 (72.34) | 18.7374 |
| 1990's | 11 (11.70) | 18.2507 |
| 2000's | 3 (3.19) | 29.6817 |
| 2010's | 10 (10.64) | 24.3611 |
| 2020's | 2 (2.13) | 2.80 |
| Authors | Studies |
|---|---|
| Mpabanzi, L | 1 |
| Wainwright, J | 1 |
| Boonen, B | 1 |
| van Eijk, H | 1 |
| Dhar, D | 1 |
| Karssemeijer, E | 1 |
| Dejong, CHC | 1 |
| Jalan, R | 1 |
| Schwartz, JM | 1 |
| Olde Damink, SWM | 1 |
| Soons, Z | 1 |
| Herter, J | 1 |
| Lederer, AK | 1 |
| Ronco, AL | 1 |
| Hannibal, L | 1 |
| Huber, R | 1 |
| Storz, MA | 1 |
| Bancel, LP | 1 |
| Germain, N | 1 |
| Guemann, AS | 1 |
| Joncquel Chevalier Curt, M | 1 |
| Dessein, AF | 1 |
| Jović-Stošić, J | 1 |
| Putić, V | 1 |
| Perković-Vukčević, N | 1 |
| Babić, G | 1 |
| Đorđević, S | 1 |
| Šegrt, Z | 1 |
| Chen, N | 1 |
| Hao, C | 1 |
| Peng, X | 1 |
| Lin, H | 1 |
| Yin, A | 1 |
| Hao, L | 1 |
| Tao, Y | 1 |
| Liang, X | 1 |
| Liu, Z | 1 |
| Xing, C | 1 |
| Chen, J | 1 |
| Luo, L | 1 |
| Zuo, L | 1 |
| Liao, Y | 1 |
| Liu, BC | 1 |
| Leong, R | 1 |
| Wang, C | 1 |
| Liu, C | 1 |
| Neff, T | 1 |
| Szczech, L | 1 |
| Yu, KP | 1 |
| Santarelli, F | 1 |
| Cassanello, M | 1 |
| Enea, A | 1 |
| Poma, F | 1 |
| D'Onofrio, V | 1 |
| Guala, G | 1 |
| Garrone, G | 1 |
| Puccinelli, P | 1 |
| Caruso, U | 2 |
| Porta, F | 1 |
| Spada, M | 1 |
| Akira, K | 1 |
| Hichiya, H | 1 |
| Morita, M | 1 |
| Shimizu, A | 1 |
| Mitome, H | 1 |
| Garlich, FM | 1 |
| Goldman, M | 1 |
| Pepe, J | 1 |
| Nelson, LS | 1 |
| Allan, MJ | 1 |
| Goldstein, DA | 1 |
| Goldfarb, DS | 1 |
| Hoffman, RS | 1 |
| Oh, JS | 1 |
| Choi, KH | 1 |
| Malhotra, RC | 1 |
| Ghia, DK | 1 |
| Cordato, DJ | 1 |
| Beran, RG | 1 |
| Jing, L | 1 |
| Chu, XP | 1 |
| Jiang, YQ | 1 |
| Collier, DM | 1 |
| Wang, B | 1 |
| Jiang, Q | 1 |
| Snyder, PM | 1 |
| Zha, XM | 1 |
| Zouaoui, K | 1 |
| Dulaurent, S | 1 |
| Gaulier, JM | 1 |
| Moesch, C | 1 |
| Lachâtre, G | 1 |
| NYHAN, WL | 10 |
| CHISOLM, JJ | 1 |
| EDWARDS, RO | 1 |
| CHILDS, B | 1 |
| CRISTOFORI, FC | 1 |
| DUNCAN, GG | 1 |
| PITTS, RF | 3 |
| PILKINGTON, LA | 2 |
| DEHAAS, JC | 1 |
| GEROK, W | 1 |
| PABST, K | 1 |
| WELCH, J | 1 |
| SAUER, F | 1 |
| Stella, J | 1 |
| Ryan, M | 1 |
| Rosa, RB | 1 |
| Schuck, PF | 1 |
| de Assis, DR | 1 |
| Latini, A | 1 |
| Dalcin, KB | 1 |
| Ribeiro, CA | 1 |
| da C Ferreira, G | 1 |
| Maria, RC | 1 |
| Leipnitz, G | 1 |
| Perry, ML | 1 |
| Filho, CS | 1 |
| Wyse, AT | 1 |
| Wannmacher, CM | 1 |
| Wajner, M | 1 |
| Cohen, MV | 1 |
| Yang, XM | 1 |
| Downey, JM | 1 |
| Soriano, JR | 1 |
| Taitz, LS | 1 |
| Finberg, L | 1 |
| Edelmann, CM | 1 |
| Bennett, MJ | 1 |
| Littlewood, JM | 1 |
| MacDonald, A | 1 |
| Pollitt, RJ | 1 |
| Thompson, J | 1 |
| Schoos-Barbette, S | 1 |
| Gerard, J | 1 |
| Francotte, N | 1 |
| Lambotte, C | 1 |
| Bartlett, K | 1 |
| Ng, H | 1 |
| Leonard, JV | 2 |
| Merinero, B | 2 |
| DelValle, JA | 1 |
| Jiménez, A | 1 |
| Garcia, MJ | 1 |
| Ugarte, M | 2 |
| Solaguren, R | 1 |
| López, O | 1 |
| Condado, I | 1 |
| Boyd, RE | 1 |
| Brennan, PT | 1 |
| Deng, JF | 1 |
| Rochester, DF | 1 |
| Spyker, DA | 1 |
| Karsten, J | 1 |
| Hansen, HG | 1 |
| Heuer, R | 1 |
| Wulff, UC | 1 |
| Kneer, J | 1 |
| Tizianello, A | 1 |
| Deferrari, G | 1 |
| Garibotto, G | 1 |
| Robaudo, C | 1 |
| Acquarone, N | 1 |
| Ghiggeri, GM | 1 |
| Hayasaka, K | 1 |
| Narisawa, K | 1 |
| Satoh, T | 1 |
| Tateda, H | 1 |
| Metoki, K | 1 |
| Tada, K | 2 |
| Hiraga, K | 1 |
| Aoki, T | 1 |
| Kawakami, T | 1 |
| Akamatsu, H | 1 |
| Matsuo, N | 1 |
| del Valle, JA | 1 |
| Pérez-Cerdá, C | 1 |
| Schutgens, RB | 1 |
| Middleton, B | 2 |
| vd Blij, JF | 1 |
| Oorthuys, JW | 1 |
| Veder, HA | 1 |
| Vulsma, T | 1 |
| Tegelaers, WH | 1 |
| Jackson, AA | 1 |
| Golden, MH | 1 |
| Pillière, F | 1 |
| Maigret, P | 1 |
| Garnier, R | 1 |
| Harry, P | 1 |
| Baud, F | 1 |
| Efthymiou, ML | 1 |
| Weinberg, JM | 2 |
| Venkatachalam, MA | 2 |
| Goldberg, H | 1 |
| Roeser, NF | 2 |
| Davis, JA | 2 |
| Jooste, S | 1 |
| Erasmus, E | 1 |
| Mienie, LJ | 1 |
| de Wet, WJ | 1 |
| Gibson, KM | 1 |
| Ito, T | 1 |
| Kidouchi, K | 1 |
| Sugiyama, N | 1 |
| Kajita, M | 1 |
| Chiba, T | 1 |
| Niwa, T | 1 |
| Wada, Y | 1 |
| Fukao, T | 1 |
| Kodama, A | 1 |
| Aoyanagi, N | 1 |
| Tsukino, R | 1 |
| Uemura, S | 1 |
| Song, XQ | 1 |
| Watanebe, H | 1 |
| Kuhara, T | 1 |
| Matsumoto, I | 1 |
| Orii, T | 1 |
| Kondo, N | 1 |
| Mályusz, M | 1 |
| Rudolph, N | 1 |
| Barth, A | 1 |
| Gronow, G | 1 |
| Mályusz, T | 1 |
| van den Berg, H | 1 |
| Boelkens, MT | 1 |
| Hommes, FA | 3 |
| Musil, J | 1 |
| Matsuda, I | 1 |
| Terashima, T | 1 |
| Yamamoto, J | 1 |
| Akaboshi, I | 1 |
| Shinozuka, S | 1 |
| Hattori, S | 1 |
| Nagata, N | 1 |
| Oka, Y | 1 |
| Lehtonen, T | 1 |
| Yudkoff, M | 1 |
| Cohn, RM | 1 |
| Puschak, R | 1 |
| Rothman, R | 1 |
| Segal, S | 1 |
| O'Brien, WE | 1 |
| Wadlington, WB | 1 |
| Kilroy, A | 1 |
| Ando, T | 7 |
| Sweetman, L | 1 |
| Rowley, BO | 1 |
| Brothers, V | 1 |
| Gerritsen, T | 3 |
| Krieger, I | 1 |
| Tanaka, K | 2 |
| Dodelson de Kremer, R | 1 |
| Depetris de Boldini, C | 1 |
| Paschini de Capra, A | 1 |
| Hliba, E | 1 |
| Corbella, L | 1 |
| Almeida, AR | 1 |
| Wetzels, JF | 1 |
| Bunnachak, D | 1 |
| Burke, TJ | 1 |
| Chaimovitz, C | 1 |
| Hammond, WS | 1 |
| Schrier, RW | 1 |
| Pesce, F | 1 |
| Cerone, R | 1 |
| Romano, C | 1 |
| Indo, Y | 1 |
| Glassberg, R | 1 |
| Yokota, I | 1 |
| Seakins, JW | 1 |
| Gompertz, D | 3 |
| Draffan, GH | 1 |
| Watts, JL | 1 |
| Hull, D | 4 |
| Eldjarn, L | 1 |
| Jellum, E | 1 |
| Stokke, O | 1 |
| Hsia, YE | 3 |
| Scully, KJ | 1 |
| Rosenberg, LE | 2 |
| Haworth, JC | 1 |
| Ford, JD | 1 |
| Storrs, CN | 1 |
| Bau, DC | 1 |
| Peters, TJ | 1 |
| Hughes, EA | 1 |
| Barnes, ND | 2 |
| Balgobin, L | 1 |
| Wei, EP | 1 |
| Thames, MD | 2 |
| Kontos, HA | 2 |
| Patterson, JL | 1 |
| Guibaud, P | 2 |
| Frimpter, GW | 1 |
| Host, WR | 1 |
| Serlin, O | 1 |
| Rush, BF | 1 |
| Keating, JP | 2 |
| Feigin, RD | 1 |
| Tenenbaum, SM | 1 |
| Hillman, RE | 2 |
| Daum, RS | 1 |
| Scriver, CR | 1 |
| Mamer, OA | 1 |
| Delvin, E | 1 |
| Lamm, P | 1 |
| Goldman, H | 1 |
| Duran, M | 1 |
| Ketting, D | 1 |
| Wadman, SK | 1 |
| Trijbels, JM | 1 |
| Bakkeren, JA | 1 |
| Waelkens, JJ | 1 |
| Brandt, IK | 1 |
| Clement, DH | 1 |
| Provence, SA | 1 |
| Bergman, EN | 1 |
| Kaufman, CF | 1 |
| Wolff, JE | 1 |
| Williams, HH | 1 |
| Rasmussen, K | 3 |
| Cottom, D | 2 |
| Donnell, G | 2 |
| Wadlington, W | 1 |
| Kilroy, AW | 1 |
| Connor, JD | 1 |
| Barnes, N | 1 |
| Lombana, A | 1 |
| Watlington, CO | 1 |
| Jessee, F | 1 |
| Centa, A | 1 |
| Pedersen, VF | 1 |
| De Groot, CJ | 2 |
| Troelstra, JA | 1 |
| Larbre, F | 1 |
| Hartemann, E | 1 |
| Collombel, C | 1 |
| Guerrier, G | 1 |
| Okken, A | 1 |
| Ferdinand, W | 1 |
| Gordon, RR | 1 |
| Owen, G | 1 |
| Christophe, J | 1 |
| Winand, J | 1 |
| Kutzner, R | 1 |
| Hebbelinck, M | 1 |
| Donnell, GN | 1 |
| Rampini, S | 1 |
| Vischer, D | 1 |
| Curtius, HC | 1 |
| Anders, PW | 1 |
| Tancredi, F | 1 |
| Frischknecht, W | 1 |
| Prader, A | 1 |
| Lilljeqvist, AC | 1 |
| Campanacci, L | 1 |
| Guarnieri, GF | 1 |
| Siliprandi, N | 1 |
| Fiaschi, E | 1 |
| Gong, L | 1 |
| Heiner, DC | 1 |
| Bray, PF | 1 |
| Lindblad, B | 1 |
| Lindblad, BS | 1 |
| Olin, P | 1 |
| Svanberg, B | 1 |
| Zetterström, R | 1 |
| Broyer, M | 1 |
| Berger, R | 1 |
| Morrow, G | 1 |
| Barness, LA | 1 |
| Auerbach, VH | 1 |
| DiGeorge, AM | 1 |
| Rehberg, ML | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of FG-4592 for Treatment of Anemia in Subjects With Chronic Kidney Disease Not on Dialysis[NCT02652819] | Phase 3 | 154 participants (Actual) | Interventional | 2015-12-31 | Completed | ||
| A Randomized Controlled Trial to Evaluate the Safety and Efficacy of Roxadustat in Patients With Acute ST Elevation Myocardial Infarction[NCT04803864] | Phase 2 | 158 participants (Anticipated) | Interventional | 2021-06-10 | Recruiting | ||
| Roxadustat Reduces the Incidence of Acute Kidney Injury After Coronary Artery Bypass Grafting: a Multicenter, Randomized, Double-blind, Placebo-controlled Study[NCT05010460] | Phase 2 | 318 participants (Anticipated) | Interventional | 2021-09-30 | Recruiting | ||
| Sodium Bicarbonate to Treat Severe Acidosis in the Critically Ill : A Multiple Center Randomized Clinical Trial (BICAR-ICU)[NCT02476253] | Phase 3 | 400 participants (Anticipated) | Interventional | 2015-05-05 | Recruiting | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for glycine and Acidosis
| Article | Year |
|---|---|
[ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].
Topics: Acidosis; Acidosis, Renal Tubular; Amino Acids; Cystinuria; Diabetes Insipidus; Glycine; Glycosuria; | 1965 |
[Propionic acidemia. New concept of hyperglycinemia with ketosis].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Glycine; Humans; Propionates | 1972 |
Aminoacidurias due to inherited disorders of metabolism. 2.
Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Arginase; Arginine; Carbamates; Citrulline; | 1973 |
2 trials available for glycine and Acidosis
| Article | Year |
|---|---|
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.
Topics: Acidosis; Adult; Aged; Anemia; Cholesterol; Double-Blind Method; Female; Glycine; Hematinics; Hemogl | 2019 |
A comparative study of Kystosol and glycine as irrigating solutions during transurethral prostatic resection.
Topics: Acetates; Acidosis; Drug Combinations; Drug Evaluation; Glycine; Humans; Male; Prostatectomy; Prosta | 1978 |
89 other studies available for glycine and Acidosis
| Article | Year |
|---|---|
Fluxomics reveals cellular and molecular basis of increased renal ammoniagenesis.
Topics: Acidosis; Amino Acids; Ammonia; Animals; Glycine; Kidney; Rats | 2022 |
Dietary Acid Load Correlates with Serum Amino Acid Concentrations after a Four-Week Intervention with Vegan vs. Meat-Rich Diets: A Secondary Data Analysis.
Topics: Acidosis; Acids; Diet; Diet, Vegan; Glutamine; Glycine; Humans; Meat; Secondary Data Analysis; Vegan | 2023 |
Abnormal Ketone Bodies in a 22-Month-Old Boy Presenting with Recurrent Vomiting and Metabolic Acidosis.
Topics: Acetoacetates; Acetyl-CoA C-Acyltransferase; Acidosis; Amino Acid Metabolism, Inborn Errors; Glycine | 2019 |
Intravenous lipid emulsion in treatment of cardiocirculatory disturbances caused by glyphosate-surfactant herbicide poisoning.
Topics: Acidosis; Electrocardiography; Fat Emulsions, Intravenous; Glycine; Glyphosate; Herbicides; Humans; | 2016 |
A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency.
Topics: Acetyl-CoA C-Acetyltransferase; Acidosis; Acute Disease; Amino Acid Metabolism, Inborn Errors; Gluta | 2013 |
Metabonomic study on the biochemical response of spontaneously hypertensive rats to chronic taurine supplementation using (1)H NMR spectroscopic urinalysis.
Topics: Acidosis; Animals; Blood Pressure; Citric Acid Cycle; Cresols; Dietary Supplements; Glycine; Magneti | 2013 |
Hemodialysis clearance of glyphosate following a life-threatening ingestion of glyphosate-surfactant herbicide.
Topics: Acidosis; Blood Chemical Analysis; Electrocardiography; Glycine; Glyphosate; Hemodynamics; Herbicide | 2014 |
Methemoglobinemia associated with metaflumizone poisoning.
Topics: Acidosis; Alcohol Drinking; Antidotes; Combined Modality Therapy; Glycine; Glyphosate; Humans; Insec | 2014 |
Glyphosate-surfactant herbicide-induced reversible encephalopathy.
Topics: Acidosis; Acute Disease; Aged; Coma; Glasgow Coma Scale; Glycine; Glyphosate; Herbicides; Humans; Ma | 2010 |
N-glycosylation of acid-sensing ion channel 1a regulates its trafficking and acidosis-induced spine remodeling.
Topics: Acid Sensing Ion Channels; Acidosis; Analysis of Variance; Animals; Animals, Newborn; Asparagine; Bi | 2012 |
Determination of glyphosate and AMPA in blood and urine from humans: about 13 cases of acute intoxication.
Topics: Accidents; Acidosis; Adult; Aged; Arrhythmias, Cardiac; Chemical and Drug Induced Liver Injury; Chro | 2013 |
Idiopathic hyperglycinuria. III. Report of a second case.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Glycine; Proteins; Urolithiasis | 1963 |
FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Blood; Child; Diet; Diet Therapy; Glycine; Humans; I | 1964 |
URIC ACID EXCRETION IN OBESE SUBJECTS DURING PERIODS OF TOTAL FASTING.
Topics: Acidosis; Basal Metabolism; Blood Glucose; Fasting; Glycine; Humans; Obesity; Pennsylvania; Probenec | 1964 |
N15 TRACER STUDIES ON THE ORIGIN OF URINARY AMMONIA IN THE ACIDOTIC DOG, WITH NOTES ON THE ENZYMATIC SYNTHESIS OF LABELED CLUTAMIC ACID AND GLUTAMINES.
Topics: Acidosis; Amino Acids; Ammonia; Blood; Chromatography; Creatine; Creatinine; Dogs; Glutamates; Gluta | 1965 |
RELATIONSHIP OF PNH3 OF TUBULAR CELLS TO RENAL PRODUCTION OF AMMONIA.
Topics: Acidosis; Alanine; Amino Acids; Ammonia; Ammonium Chloride; Animals; Aspartic Acid; Body Fluids; Dog | 1965 |
Acetoacetate and beta-hydroxy-beta-methyl glutaryl coenzyme A metabolism in normal and ketotic guinea pigs.
Topics: Acetoacetates; Acidosis; Acyl Coenzyme A; Coenzymes; Glycine; Guinea Pigs; Ketoses; Ketosis | 1961 |
Glyphosate herbicide formulation: a potentially lethal ingestion.
Topics: Acidosis; Administration, Oral; Adult; Aged; Drug Overdose; Emergency Medicine; Fatal Outcome; Glyci | 2004 |
Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetates; Acetoacetates; Acetyl-CoA C-Acyltransferase; Acidosis; A | 2005 |
The pH hypothesis of postconditioning: staccato reperfusion reintroduces oxygen and perpetuates myocardial acidosis.
Topics: Acidosis; Alkaloids; Animals; Apoptosis; Benzophenanthridines; Buffers; Carbon Dioxide; Catheterizat | 2007 |
Treatment of hyperglycinemia.
Topics: Acidosis; Agranulocytosis; Amino Acid Metabolism, Inborn Errors; Blood Platelet Disorders; Child; Ch | 1967 |
Hyperglycinemia with ketoacidosis and leukopenia. Metabolic studies on the nature of the defect.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Diet Therapy; Dietary Proteins | 1967 |
A case of beta-ketothiolase deficiency.
Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Acyltransferases; Dietary Proteins; Female; Glycine; Humans; | 1983 |
A treatment of non-ketotic hyperglycinaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Combined Modality Therapy; Deoxych | 1984 |
A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Topics: Acidosis; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Biotin; Butyrates; Carbon Dioxide; | 1980 |
Late onset type of propionic acidaemia: case report and biochemical studies.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Female; Glycine; Humans; Hydr | 1981 |
Strychnine poisoning. Recovery from profound lactic acidosis, hyperthermia, and rhabdomyolysis.
Topics: Acidosis; Adult; Body Temperature; Creatine Kinase; Female; Fever; Glycine; Humans; Hydrogen-Ion Con | 1983 |
[Vitamin-B12-dependent methylmalonic acidemia in twins].
Topics: Acidosis; Diseases in Twins; Glycine; Humans; Infant; Malonates; Metabolism, Inborn Errors; Methylma | 1983 |
Renal ammoniagenesis in an early stage of metabolic acidosis in man.
Topics: Acidosis; Adult; Amino Acids; Ammonia; Bicarbonates; Diuresis; Glutamine; Glycine; Humans; Kidney; M | 1982 |
Glycine cleavage system in ketotic hyperglycinemia: a reduction of H-protein activity.
Topics: Acidosis; Amino Acid Oxidoreductases; Carrier Proteins; Female; Glycine; Glycine Decarboxylase Compl | 1982 |
[Human fibroblast bank for studying amino acid disorders and organic acidemias].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Cell Line; Cells, Cultured; Child; Child, Preschool; | 1982 |
Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts.
Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Acyltransferases; Adult; Child; Fibroblasts; Glycine; Humans | 1982 |
[15N]Glycine metabolism in normal man: the metabolic alpha-amino-nitrogen pool.
Topics: Acidosis; Adult; Alanine; Ammonia; Deamination; Fasting; Glutamates; Glycine; Humans; Male; Nitrogen | 1980 |
[Intoxications by a weedkiller preparation containing glyphosate].
Topics: Acidosis; Acute Kidney Injury; Amylases; Burns, Chemical; Digestive System Diseases; Glycine; Glypho | 1993 |
Modulation by Gly, Ca, and acidosis of injury-associated unesterified fatty acid accumulation in proximal tubule cells.
Topics: Acidosis; Animals; Antimycin A; Biological Transport; Calcium; Cell Hypoxia; Dose-Response Relations | 1995 |
The detection of 3-methylglutarylcarnitine and a new dicarboxylic conjugate, 3-methylglutaconylcarnitine, in 3-methylglutaconic aciduria.
Topics: Acidosis; Carnitine; Chromatography, Gas; Female; Fibroblasts; Glutarates; Glycine; Humans; Hydro-Ly | 1994 |
Liquid chromatographic-atmospheric pressure chemical ionization mass spectrometric analysis of glycine conjugates and urinary isovalerylglycine in isovaleric acidemia.
Topics: Acidosis; Administration, Oral; Carnitine; Child, Preschool; Chromatography, Liquid; Female; Glucuro | 1995 |
Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytes.
Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Amino Acid Metabolism, Inborn Errors; Cell Line, Transformed | 1996 |
Hippurate as a source of renal and hepatic ammoniagenesis in different species.
Topics: Acidosis; Ammonia; Animals; Cats; Cattle; Glutamine; Glycine; Hippurates; Humans; Kidney; Kidney Tub | 1997 |
A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiency.
Topics: Acidosis; Amino Acids; Apoenzymes; Apoproteins; Glycine; Humans; Infant, Newborn; Isomerases; Male; | 1976 |
Physiological characteristics of various experimental models for the study of disorders in purine metabolism.
Topics: Acidosis; Alkalosis; Allopurinol; Animals; Cholesterol; Disease Models, Animal; Diuresis; Fructose; | 1977 |
Methylmalonic acidemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Glycine; Humans; Hypoglycemia; Infa | 1978 |
Glycine therapy in isovaleric acidemia.
Topics: Acidosis; Administration, Oral; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Drug Adminis | 1978 |
Inhibition of glycine synthase by branched-chain alpha-keto acids. A possible mechanism for abnormal glycine metabolism in ketotic hyperglycinemia.
Topics: Acidosis; Acyl Coenzyme A; Animals; Caproates; Glycine; Keto Acids; Ketosis; Liver; Male; Rats; Tran | 1978 |
Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Citrates; Coenzyme A; Creatinine; Croto | 1975 |
The vitamin B12-deficient rat as a possible model of ketotic hyperglycinemia.
Topics: Acidosis; Animals; Biotin; Carbon Dioxide; Carboxy-Lyases; Glycine; Glycine Hydroxymethyltransferase | 1975 |
Therapeutic effects of glycine in isovaleric acidemia.
Topics: Acidosis; Alkalies; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycine; Humans; Inactivati | 1976 |
[Phenotypic expression variation of isovaleric acidemia in Argentinian patients. A long term follow-up].
Topics: Acidosis; Brain; Child, Preschool; Chromatography, Thin Layer; Family; Female; Follow-Up Studies; Gl | 1992 |
Acute phosphate depletion and in vitro rat proximal tubule injury: protection by glycine and acidosis.
Topics: Acidosis; Adenosine Triphosphate; Animals; Glycine; In Vitro Techniques; Kidney Tubules, Proximal; L | 1992 |
Acute neonatal isovaleric acidaemia presented without acidosis or ketonuria.
Topics: Acidosis; Dietary Proteins; Female; Glycine; Hemiterpenes; Humans; Infant; Ketones; Male; Metabolism | 1991 |
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable matur
Topics: Acidosis; Base Sequence; Blotting, Northern; Cell Line; Electron-Transferring Flavoproteins; Flavopr | 1991 |
Role of increased cytosolic free calcium in the pathogenesis of rabbit proximal tubule cell injury and protection by glycine or acidosis.
Topics: Acidosis; Adenosine Triphosphate; Animals; Calcium; Cell Survival; Cytosol; Fura-2; Glycine; Hydroge | 1991 |
Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia.
Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acidosis; Female; Glycine; Humans | 1987 |
Biotin-responsive beta-methylcrotonylglycinuria.
Topics: Acidosis; Administration, Oral; Amino Acid Metabolism, Inborn Errors; Biotin; Butyrates; Carbon Diox | 1971 |
Application of gas chromatography-mass spectrometry in routine and research in clinical chemistry.
Topics: Acidosis; Adult; Body Fluids; Carbon Dioxide; Chemistry, Clinical; Chromatography, Gas; Clinical Lab | 1974 |
Defective propionate carboxylation in ketotic hyperglycinaemia.
Topics: Acidosis; Carbon Isotopes; Child; Coenzyme A; Female; Glycine; Humans; Infant, Newborn; Leukocytes; | 1969 |
Ketotic hyperglycinaemia.
Topics: Acidosis; Amino Acids; Child; Glycine; Humans; Lactates; Malonates; Pyruvates | 1969 |
Localisation of enzymic defect in propionicacidaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Citric Acid Cycle; Coenzyme A; Consangu | 1970 |
Biotin-responsive propionicacidaemia.
Topics: Acidosis; Biotin; Carboxy-Lyases; Child, Preschool; Chromatography, Gas; Diet Therapy; Glycine; Huma | 1970 |
Inhibition of the vasodilator effect of hypercapnic acidosis by hypercalcemia in dogs and rats.
Topics: Acidosis; Animals; Buffers; Calcium; Dogs; Glycine; Hindlimb; Hydrochloric Acid; Hypercalcemia; Hype | 1974 |
Hyperalimentation in cirrhotic patients.
Topics: Acid-Base Equilibrium; Acidosis; Alanine Transaminase; Alkaline Phosphatase; Amino Acids; Ammonia; A | 1972 |
Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Diet Therapy; Dietary Proteins | 1972 |
An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Butyrates; Cells, Cultured; Child; Child, Preschool; | 1973 |
Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered.
Topics: Acidosis; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gas; Diagnosis, Differential; Fema | 1973 |
Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".
Topics: Acetoacetates; Acidosis; Acyltransferases; Amino Acid Metabolism, Inborn Errors; Butanones; Carbon R | 1974 |
Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Body Height; Body Weight; Carboxy-Lyases; Child; Coe | 1974 |
Renal metabolism of amino acids and ammonia in fed and fasted pregnant sheep.
Topics: Acidosis; Alanine; Amino Acids; Ammonia; Animals; Arginine; Aspartic Acid; Catheterization; Citrulli | 1974 |
A block in glycine cleavage reaction as a common mechanism in ketotic and nonketotic hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon Radioisotopes; Child, Preschool; Female; Glyc | 1974 |
Excretion of propionylglycine in propionic acidaemia.
Topics: Acidosis; Acylation; Autoanalysis; Child, Preschool; Chromatography, Gas; Diet; Female; Glycine; Hum | 1972 |
The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia.
Topics: Acidosis; Body Fluids; Carbon Dioxide; Carbon Isotopes; Child, Preschool; Female; Fibroblasts; Glyci | 1972 |
Vasodilator effects of local hypercapnic acidosis in dog skeletal muscle.
Topics: Acidosis; Animals; Calcium; Carbon Dioxide; Dilatation; Dogs; Glycine; Hydrochloric Acid; Hydrogen-I | 1971 |
[A case of Ketoacidotic hyperglycinemia. 1st Italian contribution].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Infant | 1971 |
[A case of methylmalonic acid acidosis].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Infant Nutrition Disorders; | 1971 |
Nonketotic hyperglycinemia: an in vitro study of the glycine-serine conversion in liver of three patients and the effect of dietary methionine.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Biopsy; Carbon Isotopes; Culture Techniques; Diet Th | 1970 |
[Glycinosis with acidocetosis of late revelation and favorable evolution].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Glutamates; Gl | 1970 |
Nonketotic hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Glycine; Humans; Infant, Newborn; Male | 1970 |
Nonketotic hyperglycinaemia. Clinical findings and amino acid analyses on the plasma of a new case.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Diet Therapy; Dietary Proteins; Fe | 1970 |
Metabolism of amino acids by the perfused rat kidney.
Topics: Acidosis; Alanine; Amino Acids; Ammonia; Animals; Aspartic Acid; Glucose; Glutamates; Glutamine; Gly | 1971 |
Amino acid levels in plasma, liver, muscle, and kidney during and after exercise in fasted and fed rats.
Topics: Acidosis; Alanine; Amino Acids; Animals; Aspartic Acid; Fasting; Gluconeogenesis; Glutamates; Glutam | 1971 |
Propionic acidemia in patients with ketotic hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Coenzy | 1971 |
[Hereditary hyperglycinemia. Clinical picture and determination of glycoxylic and oxalic acids in the urines of one patient each with acidotic and nonacidotic form].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Body Weight; Creatinine; Female; Glycine; Glyoxylate | 1967 |
Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Chromatography, Thin Layer; Coenzyme A; Dietary Prot | 1968 |
Importance of the single case.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Coenzyme A; Glycine; Humans; Infant; Intellectual Di | 1968 |
Metabolic studies of acetoacetate, pyruvate, lactate and citrate in uremic acidosis.
Topics: Acetoacetates; Acidosis; Analysis of Variance; Chronic Disease; Citrates; Citric Acid Cycle; Creatin | 1968 |
Metabolism of glycine in the nonketotic form of hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon Dioxide; Carbon Isotopes; Child; Child, Presc | 1968 |
Methylmalonic acidemia. A disorder associated with acidosis, hyperglycinemia, and hyperlactatemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Bicarbonates; Child, Preschool; Diet Th | 1968 |
[Glycinosis (hyperglycinemia)].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child Development; Child, Preschool; Ch | 1968 |
Observations on the coexistence of methylmalonic acidemia and glycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Female; Genes, Recessive; Glycine; Hepatomegaly; Hum | 1969 |
Metabolism of glyoxylate in nonketotic hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon Dioxide; Carbon Isotopes; Child; Child, Presc | 1969 |