Page last updated: 2024-08-17

methionine and Deficiency, Mental

methionine has been researched along with Deficiency, Mental in 77 studies

Research

Studies (77)

Timeframe	Studies, this research(%)	All Research%
pre-1990	70 (90.91)	18.7374
1990's	2 (2.60)	18.2507
2000's	3 (3.90)	29.6817
2010's	1 (1.30)	24.3611
2020's	1 (1.30)	2.80

Authors

Authors	Studies
Aukland, SM; Elgen, IB; Fehn, JR; Fevang, SKE; Irgens, H; Njølstad, PR; Sirnes, E; Sulen, Å; Svalastoga, P; Valen, E	1
Baumgartner, MR; Burda, P; Chinnery, PF; Demirkol, M; Dionisi-Vici, C; Dobbelaere, D; Fowler, B; Froese, DS; Gökcay, G; Häberle, J; Huemer, M; Lossos, A; Mengel, E; Morris, AA; Mulder-Bleile, R; Niezen-Koning, KE; Parini, R; Plecko, B; Rokicki, D; Schiff, M; Schimmel, M; Sewell, AC; Sperl, W; Spiekerkoetter, U; Steinmann, B; Suormala, T; Taddeucci, G; Trefz, F; Trejo-Gabriel-Galán, JM; Tsuji, M; Vilaseca, MA; von Kleist-Retzow, JC; Walker, V; Zeev, BB; Zeman, J	1
Jiang, T; Li, J; Li, K; Li, Y; Liu, B; Liu, Y; Shu, N; Song, M; Yu, C; Zhou, Y; Zhu, W	1
FINKELSTEIN, JD; IRREVERRE, F; LASTER, L; MUDD, SH	2
GERRITSEN, T; WAISMAN, HA	1
ANTENER, I; HOOFT, C; OYAERT, W; SNOECK, J; TIMMERMANS, J; VANDENHENDE, C	1
CARSON, NA; DENT, CE; FIELD, CM; GAULL, GE	1
BRENTON, DP; CUSWORTH, DC; GAULL, GE	1
HOLT, LE; NORTON, PM; ROITMAN, E; SNYDERMAN, SE	1
Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J	1
Waisman, HA	1
Frimpter, GW; Fuchs, F; Greenberg, AJ; Hilgartner, M	1
Carson, NA	2
Hansen, S; MacDougall, L; Perry, TL; Warrington, PD	1
Martenet, AC; Speiser, P; Witmer, R	1
Chase, HP; Goodman, SI; O'Brien, D	1
Arakawa, T; Dancis, J; Hutzler, J; Morikawa, T; Tada, K; Wada, Y	1
Carton, D; Hooft, C	1
Arakawa, T; Hirono, H; Tada, K; Yoshida, T	1
Schneiderman, LJ	1
Gardner, AP; Howell, RT; McDermott, A	1
Howard-Peebles, PN; Pryor, JC	1
Bender, AN; Gaull, GE; Schaffner, F; Tallan, HH; Vulovic, D	1
Bakker, C; Galjaard, H; Hoogeveen, AT; Oostra, BA; Sacchi, N; Tamanini, F; Van Unen, L	1
Bassan, H; Fattal-Valevski, A; Gutman, A; Harel, S; Korman, SH; Lerman-Sagie, T	1
Enzenauer, J; Matz, D; Menne, F	1
Brunet, C; Charpentier, C; Labrune, P; Lutun, H; Odievre, M; Perignon, JL; Rault, M; Saudubray, JM	1
Andria, G; Boers, GH; Bromberg, IL; Cerone, R; Levy, HL; Mudd, SH; Pettigrew, KD; Pyeritz, RE; Skovby, F; Wilcken, B	1
Bracken, P; Coll, P	1
Corbeel, L; Eeckels, R; Jaeken, J; Van den Berghe, G; Van Tornout, J	1
Crawford, LE; Hansen, S; Love, DL; Perry, TL; Tischler, B	1
Donnell, GN; Koch, R; Lieberman, E; Shaw, KN	1
Fekete, G	1
Sviatkina, OB; Vel'tishchev, IuE	1
Crawhall, JC; Purkiss, P; Stanbury, JB	1
Gröbe, H	1
Oldendorf, WH	1
de Groot, CJ; Grüttner, R; Koepp, P; Rybak, C	1
Gebala, A; Kozlowska, T	1
Iivanainen, M; Palo, J; Savolainen, H	1
AvRuskin, TW; Kang, ES	1
Dillon, MJ; England, JM; Gompertz, D; Goodey, PA; Grant, DB; Hussein, HA; Linnell, JC; Matthews, DM; Mudd, SH; Newns, GH; Seakins, JW; Uhlendorf, BW; Wise, IJ	1
Menne, F	1
Hagge, W	1
Cernea, P; Zbranca, E	1
Oldendorf, WH; Silverstein, A; Sisson, BW	1
van der Horst, JL; Wadman, SK	1
Griffiths, MI	1
Bir, K; Crawhall, JC; Purkiss, P; Stanbury, JB	1
Alpers, DH; Bartoscas, CS; Bixby, EM; Shih, VE; Thier, SO	1
Berger, R; Broyer, M	1
Chiang-Teng, C; Clark, SH; Dassell, SW; Scott, CR; Swedberg, KR	1
De Groot, CJ; Hommes, FA; Troelstra, JA	1
Agrawal, HC; Bone, AH; Davison, AN	1
Falk, W	1
Narayanan, HS; Rao, R; Reddy, GN; Sridhara, BS	1
Lowman, JT; Ulstrom, RA; Walker, WA	1
Gjessing, LR	1
Anders, PW; Curtius, HC; Martenet, AC	1
Mudd, SH; Uhlendorf, BW	1
Antener, I; Carton, D; Hooft, C; Snoeck, J; Timmermans, J; van den Hende, C	1
Antener, I; Hooft, C	1
Ketting, D; Maas, JW; van Sprang, FJ; Wadman, SK	1
Gershon, ES; Shader, RI	1
Harper, JR; Parkinson, MS	1
Schimke, RN; Spiro, HR; Welch, JP	1
Araki, S; Cowen, D; Rowland, LP; Thompson, HL; White, HH	1
Antener, I; Hooft, C; Oyaert, W; Snoeck, J; Timmermans, J; Van den Hende, C	2
Berlow, S	1
Dolman, CL; Dunn, HG; Perry, TL	1
Cusworth, DC; Komrower, GM; Lambert, AM; Westall, RG	1
Gaitonde, MK; Gaull, G	1

Reviews

3 review(s) available for methionine and Deficiency, Mental

Article	Year
[Hereditary anomalies of methionine metabolism in children]. Pediatriia, 1972, Volume: 51, Issue:4 Topics: Age Factors; Child; Flatfoot; Folic Acid; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Kyphosis; Marfan Syndrome; Metabolism, Inborn Errors; Methionine; Scoliosis	1972
[Feeble mindedness caused by genetic disorders of amino acid metabolism]. Hippokrates, 1968, May-31, Volume: 39, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine	1968
Too much of a good thing. Food and cosmetics toxicology, 1971, Volume: 9, Issue:1 Topics: Amino Acids; Animals; Blood Pressure; Central Nervous System; Eye Diseases; Food Additives; Glutamates; Glycine; Hepatic Encephalopathy; Humans; Hypothalamus; Intellectual Disability; Metabolism, Inborn Errors; Methionine; Mice; Nausea; Necrosis; Neurons; Rats; Retina; Vomiting	1971

Other Studies

74 other study(ies) available for methionine and Deficiency, Mental

Article	Year
Intellectual Disability in K Diabetes care, 2020, Volume: 43, Issue:3 Topics: Adolescent; Amino Acid Substitution; Case-Control Studies; Child; Child, Preschool; Codon, Nonsense; Cohort Studies; Diabetes Mellitus, Type 1; Female; Genetic Association Studies; Genotype; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Male; Methionine; Mutation, Missense; Norway; Potassium Channels, Inwardly Rectifying; Sulfonylurea Receptors; Valine	2020
Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency. Journal of inherited metabolic disease, 2016, Volume: 39, Issue:1 Topics: Ataxia; Betaine; Child; Female; Folic Acid; Genetic Association Studies; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Mutation; Phenotype; Psychotic Disorders; Retrospective Studies; Spinal Cord Diseases; Vitamin B 12	2016
COMT val158met modulates association between brain white matter architecture and IQ. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009, Apr-05, Volume: 150B, Issue:3 Topics: Adolescent; Adult; Amino Acid Substitution; Anisotropy; Brain; Case-Control Studies; Catechol O-Methyltransferase; Diagnostic and Statistical Manual of Mental Disorders; Diffusion Magnetic Resonance Imaging; Female; Frontal Lobe; Hippocampus; Humans; Intellectual Disability; Intelligence; Intelligence Tests; Male; Methionine; Nerve Fibers, Myelinated; Radiography; Valine; Young Adult	2009
HOMOCYSTINURIA: AN ENZYMATIC DEFECT. Science (New York, N.Y.), 1964, Mar-27, Volume: 143, Issue:3613 Topics: Amino Acids; Blood Protein Disorders; Carbon Isotopes; Child; Cystic Fibrosis; Cystinuria; Fatty Liver; Homocystinuria; Humans; Hypoproteinemia; Intellectual Disability; Ligases; Liver; Methionine; Pancreatic Neoplasms; Proteins; Psoriasis	1964
HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE. Pediatrics, 1964, Volume: 33 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Biochemical Phenomena; Biochemistry; Child; Homocystinuria; Humans; Infant; Intellectual Disability; Kidney; Metabolic Diseases; Methionine; Pathology; Proteins; Renal Aminoacidurias; Urologic Diseases	1964
METHIONINE MALABSORPTION IN A MENTALLY DEFECTIVE CHILD. Lancet (London, England), 1964, Jul-04, Volume: 2, Issue:7349 Topics: Amino Acid Metabolism, Inborn Errors; Child; Congenital Abnormalities; Diarrhea; Diarrhea, Infantile; Feces; Hair; Humans; Hydroxybutyrates; Intellectual Disability; Intestines; Methionine; Proteins; Respiration Disorders; Respiratory Tract Diseases; Seizures; Urine	1964
HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES. The Journal of pediatrics, 1965, Volume: 66 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Bone Diseases; Brain; Brain Diseases; Cardiovascular Diseases; Cerebrospinal Fluid; Child; Chromatography; Congenital Abnormalities; Eye Diseases; Facial Expression; Fatty Liver; Foot Diseases; Genetics, Medical; Homocystinuria; Humans; Hydro-Lyases; Infant; Intellectual Disability; Lens, Crystalline; Liver; Metabolism; Methionine; Urine	1965
HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS. The Journal of pediatrics, 1965, Volume: 67 Topics: Amino Acid Metabolism, Inborn Errors; Blood; Child; Genetics, Medical; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Metabolism; Methionine; Neomycin; Urine	1965
A new finding in maple-syrup-urine disease. Lancet (London, England), 1962, Jan-06, Volume: 1, Issue:7219 Topics: Acer; Child; Humans; Infant; Intellectual Disability; Leucine; Maple Syrup Urine Disease; Metabolic Diseases; Methionine	1962
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human molecular genetics, 2007, Jan-01, Volume: 16, Issue:1 Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors	2007
Some theoretical considerations in the treatment of homocystinuria. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Diet Therapy; Histidine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; L-Serine Dehydratase; Liver; Methionine; Rats	1967
Cystathioninuria: management. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Amniotic Fluid; Child; Child, Preschool; Cystine; Female; Humans; In Vitro Techniques; Intellectual Disability; Liver; Male; Methionine; Middle Aged; Pregnancy; Pyridoxal Phosphate; Pyridoxine; Thrombocytopenia	1967
Homocystinuria. Trial treatment of a 5-year old severely retarded child with a natural diet low in methionine. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Body Height; Body Weight; Child, Preschool; Cystine; Diet Therapy; Female; Growth; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Methionine; Neurologic Manifestations	1967
Sulfur-containing amino acids in the plasma and urine of homocystinurics. Clinica chimica acta; international journal of clinical chemistry, 1967, Volume: 15, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Homocysteine; Homocystine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Iodoacetates; Methionine; Sulfoxides; Sulfur; Ultraviolet Rays	1967
[Ocular changes in homocystinuria]. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1967, Volume: 154, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Child; Diagnosis, Differential; Eye Manifestations; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Methionine	1967
Treatment of homocystinuria. Archives of disease in childhood, 1967, Volume: 42, Issue:225 Topics: Amino Acid Metabolism, Inborn Errors; Child; Diet Therapy; Female; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Pedigree	1967
Hypervalinemia. A defect in valine transamination. Pediatrics, 1967, Volume: 39, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Carbon Isotopes; Child, Preschool; Female; Fetal Diseases; Humans; Intellectual Disability; Isoleucine; Japan; Keto Acids; Leucine; Leukocytes; Methionine; Phenylalanine; Placenta; Pregnancy; Transaminases; Valine	1967
[Homocystinuria]. Verhandelingen - Koninklijke Vlaamse Academie voor Geneeskunde van Belgie, 1967, Volume: 29, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Heterozygote; Homocystinuria; Humans; Intellectual Disability; Male; Methionine	1967
Homocystinuria: amino acid pattern of the liver. The Tohoku journal of experimental medicine, 1967, Volume: 92, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Child, Preschool; Cystine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Liver; Male; Methionine	1967
Latent cystathioninuria. Journal of medical genetics, 1967, Volume: 4, Issue:4 Topics: Adult; Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Female; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Pedigree	1967
Fragile X chromosome: consistent demonstration of fragile site in fibroblast cultures. Lancet (London, England), 1982, Jan-09, Volume: 1, Issue:8263 Topics: Adult; Aged; Cells, Cultured; Chromosome Fragile Sites; Chromosome Fragility; Cytological Techniques; Female; Fibroblasts; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Sex Chromosomes; X Chromosome	1982
Fragile sites in human chromosomes I. The effect of methionine on the Xq fragile site. Clinical genetics, 1981, Volume: 19, Issue:4 Topics: Cells, Cultured; Chromosome Banding; Chromosome Fragile Sites; Chromosome Fragility; Culture Media; Female; Genetic Markers; Humans; Intellectual Disability; Male; Methionine; Sex Chromosomes; X Chromosome	1981
Methioninemia and myopathy: a new disorder. Annals of neurology, 1981, Volume: 9, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child; Diagnosis, Differential; Female; Humans; Intellectual Disability; Liver; Methionine; Methionine Adenosyltransferase; Microscopy, Electron; Muscles; Muscular Diseases; Syndrome	1981
Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P. The Biochemical journal, 1999, Nov-01, Volume: 343 Pt 3 Topics: Animals; Chromatography, Gel; COS Cells; Fragile X Mental Retardation Protein; Fragile X Syndrome; Humans; Intellectual Disability; Methionine; Molecular Weight; Nerve Tissue Proteins; Recombinant Proteins; RNA-Binding Proteins; Sulfur Radioisotopes; Transfection	1999
Methylenetetrahydrofolate reductase deficiency: importance of early diagnosis. Journal of child neurology, 2000, Volume: 15, Issue:8 Topics: Betaine; Child, Preschool; Diagnosis, Differential; Fatal Outcome; Fibroblasts; Folic Acid; Hematinics; Homocysteine; Homocystinuria; Homozygote; Humans; Infant; Intellectual Disability; Lipotropic Agents; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Treatment Outcome	2000
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2]. Medizinische Klinik, 1976, Apr-30, Volume: 71, Issue:18 Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases	1976
Familial hypermethioninemia partially responsive to dietary restriction. The Journal of pediatrics, 1990, Volume: 117, Issue:2 Pt 1 Topics: Adenosylhomocysteinase; Amino Acid Metabolism, Inborn Errors; Failure to Thrive; Female; Humans; Hydrolases; Infant, Newborn; Intellectual Disability; Jaundice, Neonatal; Liver; Methionine	1990
The natural history of homocystinuria due to cystathionine beta-synthase deficiency. American journal of human genetics, 1985, Volume: 37, Issue:1 Topics: Adolescent; Adult; Child; Child, Preschool; Clinical Enzyme Tests; Cystathionine beta-Synthase; Female; Fertility; Follow-Up Studies; Genetic Testing; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Lens Subluxation; Male; Methionine; Osteoporosis; Pregnancy; Pregnancy Complications; Pyridoxine; Seizures; Surveys and Questionnaires; Thromboembolism	1985
Homocystinuria and schizophrenia. Literature review and case report. The Journal of nervous and mental disease, 1985, Volume: 173, Issue:1 Topics: Adult; Animals; Chronic Disease; Female; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Mice; Rats; Schizophrenia	1985
Congenital folate malabsorption. European journal of pediatrics, 1985, Volume: 143, Issue:4 Topics: Anemia, Macrocytic; Anemia, Megaloblastic; Biological Transport; Blood-Brain Barrier; Brain Diseases; Calcinosis; Female; Folic Acid; Folic Acid Deficiency; Humans; Infant; Infections; Intellectual Disability; Intestinal Absorption; Methionine; Seizures	1985
Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor. Lancet (London, England), 1968, Aug-31, Volume: 2, Issue:7566 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Choline; Cystine; Diet Therapy; Female; Follow-Up Studies; Homocystine; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Pyridoxine; Thrombosis	1968
Cystathioninuria. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschool; Cysteine; Diet Therapy; Female; Galactosemias; Glycogen; Humans; Infant; Intellectual Disability; Liver Neoplasms; Male; Maple Syrup Urine Disease; Methionine; Middle Aged; Neuroblastoma; Phenylketonurias; Portal Vein; Pyridoxine; Serine; Sulfisoxazole; Tyrosine	1967
[Amino acid imbalance as a pathogenetic factor in mental retardation (author's transl)]. Klinische Wochenschrift, 1974, May-15, Volume: 52, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain Chemistry; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Intellectual Disability; Leucine; Methionine; Phenylalanine; Phenylketonurias; Rats; Tyrosine; Valine	1974
Metabolism of sulfur-containing amino acids in a patient excreting -mercaptolactate-cysteine disulfide. Biochemical medicine, 1973, Volume: 7, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Cysteine; Cystine; Disulfides; Humans; Intellectual Disability; Lactates; Male; Methionine; Sulfur; Sulfur Isotopes; Taurine; Time Factors	1973
[Homocystinuria: clinical picture, therapy and results in 8 patients]. Deutsche medizinische Wochenschrift (1946), 1973, Jul-06, Volume: 98, Issue:27 Topics: Body Weight; Child; Child, Preschool; Cystine; Dietary Proteins; Female; Hair; Homocystine; Homocystinuria; Humans; Infant; Intellectual Disability; Methionine; Pyridoxine	1973
Saturation of blood brain barrier transport of amino acids in phenylketonuria. Archives of neurology, 1973, Volume: 28, Issue:1 Topics: Amino Acids; Animals; Arginine; Blood-Brain Barrier; Brain; Carbon Isotopes; Dihydroxyphenylalanine; Female; Histidine; Humans; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Methionine; Ornithine; Phenylalanine; Phenylketonurias; Rats; Threonine; Tryptophan; Tyrosine; Valine	1973
Clinical finding and therapeutic problems in non-ketotic hyperglycinemia. Helvetica paediatrica acta, 1973, Volume: 28, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Carbon Radioisotopes; Diet Therapy; Glycine; Humans; Hypotension; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Male; Methionine; Seizures	1973
The role of homocystinuria in the etiopathogenesis of children's mental deficiency. Acta Universitatis Carolinae. Medica. Monographia, 1973, Volume: 56 Topics: Adolescent; Age Factors; Amino Acids; Child, Preschool; False Positive Reactions; Homocystine; Homocystinuria; Humans; Intellectual Disability; Methionine; Methods; Vision Disorders	1973
Free amino acids and carbohydrates in the cerebrospinal fluid of 305 mentally retarded patients: a screening study. Journal of mental deficiency research, 1973, Volume: 17, Issue:2 Topics: Adolescent; Adult; Alanine; Amino Acids; Arginine; Carbohydrates; Child; Child, Preschool; Chromatography, Thin Layer; Cystine; Epilepsy; Female; Glutamates; Glutamine; Humans; Intellectual Disability; Intelligence Tests; Isoleucine; Leucine; Lysine; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Ornithine; Phenylalanine; Pneumoencephalography; Threonine; Valine	1973
Cystathioninuria, mental retardation, and juvenile diabetes mellitus. American journal of diseases of children (1960), 1974, Volume: 127, Issue:2 Topics: Adolescent; Child; Consanguinity; Cystathionine; Diabetes Mellitus; Diabetes Mellitus, Type 1; Homozygote; Humans; Intellectual Disability; Male; Methionine; Pyridoxine; Vitamin B 6 Deficiency	1974
Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism. Clinical science and molecular medicine, 1974, Volume: 47, Issue:1 Topics: Amino Acid Isomerases; Amino Acids; Anemia, Macrocytic; Autopsy; Brain; Brain Chemistry; Cells, Cultured; Child; Culture Media; Fibroblasts; Homocysteine; Humans; Intellectual Disability; Liver; Lung; Lyases; Malonates; Metabolism, Inborn Errors; Methionine; Spleen; Vitamin B 12	1974
Chemical pathology of amino acid diseases. Acta neurologica et psychiatrica Belgica, 1968, Volume: 68, Issue:4 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child, Preschool; Female; Homocystine; Humans; Hypoglycemia; Infant; Intellectual Disability; Leucine; Male; Maple Syrup Urine Disease; Methionine; Pyridoxine; Valine	1968
[Amino acid metabolism and mental retardation]. Die Medizinische Welt, 1972, Apr-15, Volume: 23, Issue:16 Topics: Diet Therapy; Female; Homocystinuria; Humans; Intellectual Disability; Intelligence; Male; Methionine; Phenylalanine; Phenylketonurias; Pregnancy; Pyridoxine	1972
[Homocystinuria and Marfan's syndrome]. Annales d'oculistique, 1972, Volume: 205, Issue:2 Topics: Adolescent; Adult; Cervical Vertebrae; Child; Female; Growth Disorders; Homocystinuria; Humans; Intellectual Disability; Lens, Crystalline; Male; Marfan Syndrome; Methionine; Osteoporosis; Pedigree; Spine	1972
Brain uptake of selenomethionine Se 75. II. Reduced brain uptake of selenomethionine Se 75 in phenylketonuria. Archives of neurology, 1971, Volume: 24, Issue:6 Topics: Blood-Brain Barrier; Brain; Humans; Injections, Intravenous; Intellectual Disability; Methionine; Phenylalanine; Phenylketonurias; Radioisotopes; Radiometry; Selenium	1971
A variant form of branched-chain keto aciduria. Acta paediatrica Scandinavica, 1971, Volume: 60, Issue:5 Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine	1971
Implications for clinical implementation of results of metabolic screening for amino acidopathies in the newborn. Archives of disease in childhood, 1971, Volume: 46, Issue:250 Topics: Amino Acid Metabolism, Inborn Errors; Follow-Up Studies; Histidine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature, Diseases; Intellectual Disability; Mass Screening; Methionine; Proline	1971
Sulfur amino acids as precursors of beta-mercaptolactate-cysteine disulfide in human subjects. Biochemical medicine, 1971, Volume: 5, Issue:2 Topics: Adult; Anilides; Cysteine; Diet; Dietary Proteins; Disulfides; Electrophoresis; Female; Humans; Intellectual Disability; Lactates; Male; Metabolism; Methionine; Models, Biological; Neomycin; Phthalic Acids; Pyridoxine; Sulfates; Sulfathiazoles; Sulfur; Taurine; Thiosulfates	1971
Studies of intestinal transport defect in Hartnup disease. Gastroenterology, 1971, Volume: 61, Issue:4 Topics: Adolescent; Biological Transport; Carbon Isotopes; Child; Culture Techniques; Feces; Genes, Recessive; Hartnup Disease; Humans; Intellectual Disability; Intestinal Mucosa; Jejunum; Leucine; Lysine; Male; Methionine; Phenylalanine; Proline; Tryptophan	1971
[Cystathioninuria]. La Presse medicale, 1969, Oct-22, Volume: 77, Issue:44 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Chromosome Aberrations; Chromosome Disorders; Humans; Intellectual Disability; Methionine; Pyridoxine	1969
Cystathioninemia: a benign genetic condition. The Journal of pediatrics, 1970, Volume: 76, Issue:4 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Butyrates; Child; Child, Preschool; Congenital Abnormalities; Cysteine; Female; Homozygote; Humans; Intellectual Disability; Keto Acids; Male; Methionine; Pyridoxine	1970
Nonketotic hyperglycinemia: an in vitro study of the glycine-serine conversion in liver of three patients and the effect of dietary methionine. Pediatric research, 1970, Volume: 4, Issue:3 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Biopsy; Carbon Isotopes; Culture Techniques; Diet Therapy; Female; Glycine; Humans; Infant; Infant, Newborn; Intellectual Disability; Liver; Methionine; Serine	1970
Effect of phenylalanine on protein synthesis in the developing rat brain. The Biochemical journal, 1970, Volume: 117, Issue:2 Topics: Acetates; Age Factors; Animals; Brain; Carbon Isotopes; Female; Glycine; Humans; Intellectual Disability; Leucine; Male; Methionine; Myelin Sheath; Phenylalanine; Phenylketonurias; Protein Biosynthesis; Rats; Sulfur Isotopes	1970
[Abortive form of homocystinuria]. Wiener klinische Wochenschrift, 1970, Oct-18, Volume: 82, Issue:42 Topics: Adolescent; Child, Preschool; Chromatography; Chromatography, Paper; Diagnosis, Differential; Eye Diseases; Female; Follow-Up Studies; Homocystine; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Methionine; Myopia; Vitreous Body	1970
Homocystinuria in three Indian children. The Indian journal of medical research, 1971, Volume: 59, Issue:4 Topics: Abnormalities, Multiple; Child; Child, Preschool; Diagnosis, Differential; Female; Homocystinuria; Humans; Intellectual Disability; Male; Methionine	1971
Albumin synthesis rates in patients with hypoproteinemia. The Journal of pediatrics, 1971, Volume: 78, Issue:5 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anaphylaxis; Anorexia Nervosa; Bile Ducts; Child; Child, Preschool; Chromatography, Gel; Colitis, Ulcerative; Cystic Fibrosis; Female; Glomerulonephritis; Humans; Hypoproteinemia; Infant; Injections, Intravenous; Intellectual Disability; Kinetics; Liver; Liver Cirrhosis; Liver Cirrhosis, Biliary; Liver Diseases; Male; Methionine; Nephrotic Syndrome; Psychomotor Disorders; Purpura; Radioisotopes; Selenium; Serum Albumin; Spectrophotometry; Tyrosine	1971
[Defects in the metabolism of methionine: methioninemia, homocystinurie, homoserinuria and cystinuria]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1967, Feb-01, Volume: 87, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Cystinuria; Homocystinuria; Humans; Intellectual Disability; Methionine	1967
[Determination of free amino acids in aqueous humor of homocystinuria patients and in control subjects]. Clinica chimica acta; international journal of clinical chemistry, 1968, Volume: 19, Issue:3 Topics: Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aqueous Humor; Autoanalysis; Child; Homocystine; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Methionine; Middle Aged	1968
Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria. Science (New York, N.Y.), 1968, May-31, Volume: 160, Issue:3831 Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Culture Techniques; Fibroblasts; Homocystine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Methionine; Skin; Transferases	1968
Further investigations in the methionine malabsorption syndrome. Helvetica paediatrica acta, 1968, Volume: 23, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Height; Body Weight; Child; Child, Preschool; Diarrhea; Feces; Female; Humans; Hydroxybutyrates; Intellectual Disability; Keto Acids; Malabsorption Syndromes; Methionine; Pedigree; Seizures	1968
Methionine malabsorption syndrome. Bibliotheca paediatrica, 1968, Volume: 87 Topics: Amino Acids; Diarrhea; Diet Therapy; Feces; Female; Homocystinuria; Humans; Hydroxybutyrates; Intellectual Disability; Malabsorption Syndromes; Male; Methionine; Pedigree; Seizures	1968
An exceptional case of tyrosinosis. Journal of mental deficiency research, 1968, Volume: 12, Issue:4 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ascorbic Acid; Cataract; Female; Humans; Intellectual Disability; Mandelic Acids; Methionine; Mixed Function Oxygenases; Phenylacetates; Phenylpyruvic Acids; Tyrosine	1968
Screening for aminoacidurias in psychiatric inpatients. Archives of general psychiatry, 1969, Volume: 21, Issue:1 Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Brain Damage, Chronic; Depression; Drug Synergism; Hartnup Disease; Homocystinuria; Hospitals, Psychiatric; Humans; Intellectual Disability; Mass Screening; Massachusetts; Mental Disorders; Methionine; Monoamine Oxidase Inhibitors; Neurotic Disorders; Personality Disorders; Phenylketonurias; Schizophrenia; Substance-Related Disorders; Tryptophan	1969
Therapeutic problems of adolescent homocystinuria. Proceedings of the Royal Society of Medicine, 1969, Volume: 62, Issue:9 Topics: Child; Diet Therapy; Homocystine; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Thromboembolism	1969
Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine. The Journal of clinical investigation, 1965, Volume: 44, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Ion Exchange; Cysteine; Humans; Hydro-Lyases; Intellectual Disability; Liver; Methionine; Sulfates; Urine	1965
Homocystinuria due to cystathionine synthase deficiency. Annals of internal medicine, 1965, Volume: 63, Issue:6 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Female; Homocysteine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; In Vitro Techniques; Intellectual Disability; Liver; Methionine	1965
Schizophrenia in a patient with a defect in methionine metabolism. The Journal of nervous and mental disease, 1965, Volume: 141, Issue:3 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain; Female; Homocysteine; Humans; Intellectual Disability; Methionine; Schizophrenia	1965
Homocystinuria. Archives of neurology, 1965, Volume: 13, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Brain; Child; Child, Preschool; Female; Homocysteine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; In Vitro Techniques; Intellectual Disability; Intracranial Embolism and Thrombosis; Lens, Crystalline; Male; Methionine; Seizures	1965
Methionine malabsorption syndrome. Annales paediatrici. International review of pediatrics, 1965, Volume: 205, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Diarrhea; Diet Therapy; Electroencephalography; Female; Humans; Infant; Intellectual Disability; Methionine; Seizures; Urine	1965
[Methionine malabsorption]. Verhandelingen - Koninklijke Vlaamse Academie voor Geneeskunde van Belgie, 1966, Volume: 28, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Humans; Intellectual Disability; Malabsorption Syndromes; Methionine	1966
Studies in cystathioninemia. American journal of diseases of children (1960), 1966, Volume: 112, Issue:2 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Cystinuria; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Methionine; Pyridoxine	1966
Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis. Neurology, 1966, Volume: 16, Issue:4 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Animals; Blood; Blood Coagulation Disorders; Brain; Child; Child, Preschool; Cystine; Electroencephalography; Female; Homocysteine; Homocystine; Homocystinuria; Humans; In Vitro Techniques; Infant; Intellectual Disability; Intracranial Embolism and Thrombosis; Kidney Diseases; Male; Methionine; Taurine; Urine	1966
Dietary treatment of homocystinuria. Archives of disease in childhood, 1966, Volume: 41, Issue:220 Topics: Amino Acid Metabolism, Inborn Errors; Body Height; Body Weight; Cystine; Diet Therapy; Female; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Methionine	1966
Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency. Journal of medical genetics, 1966, Volume: 3, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Paper; Cystine; Homocysteine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Lens, Crystalline; Male; Methionine; Middle Aged; Sulfur Isotopes	1966