Page last updated: 2024-08-17

methionine and Developmental Disabilities

methionine has been researched along with Developmental Disabilities in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (7.69)	18.7374
1990's	3 (23.08)	18.2507
2000's	5 (38.46)	29.6817
2010's	4 (30.77)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abbott, GW; Alachkar, A; Civelli, O; Hamzeh, AR; Lee, SM; Sanathara, N; Wang, L; Wang, Z; Xu, X; Yoshimura, R	1
Rogers, E; Shea, TB	1
Berry, SA; Bishop, L; Charnas, L; Kanoff, R; Krenzel, C; Schimmenti, LA	1
Stover, PJ	1
Hattersley, AT; Jones, AG	1
Balasubramaniam, S; Bjursell, MK; Blom, HJ; Brandberg, G; Cayuela, JA; Engvall, ML; Falkenberg, M; Gustafsson, CM; Halldin, M; Jakobs, C; Lesko, N; Lundeberg, J; Smith, D; Struys, E; von Döbeln, U; Wedell, A	1
Robertson, SP	1
Antonarakis, SE; Gothelf, D; Hallmayer, JF; Hinard, C; Hoeft, F; Morris, MA; Reiss, AL; Stoecker, JV	1
Buckley, MF; Elakis, G; Gardener, G; Inglis, G; Roscioli, T; Susman, RD; Zankl, A	1
Boles, RG; Horwich, AL; Kratz, LE; Ment, LR; Meyn, MS; Rinaldo, P	1
Arnold, G; Barness, LA; Harding, CO; Rosenblatt, DS; Wolff, JA	1
Bamshad, MJ; Bellus, GA; Curry, CJ; Dorst, J; Francomano, CA; Hurko, O; Jabs, EW; Lachman, RS; Lee, RR; Przylepa, KA; Rimoin, DL; Wilcox, WR	1
Bierich, JR; Fryklund, LM; Ranke, MB	1

Reviews

2 review(s) available for methionine and Developmental Disabilities

Article	Year
Lifetime requirement of the methionine cycle for neuronal development and maintenance. Current opinion in psychiatry, 2014, Volume: 27, Issue:2 Topics: Developmental Disabilities; Female; Folic Acid; Homocysteine; Humans; Methionine; Pregnancy; Prenatal Care; S-Adenosylmethionine; Vitamin B 12; Vitamin B Complex	2014
Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review. American journal of medical genetics, 1997, Sep-05, Volume: 71, Issue:4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Macrocytic; Anemia, Megaloblastic; Anorexia; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Genetic Complementation Test; Homocystine; Homocystinuria; Humans; Male; Methionine; Skin; Vitamin B 12	1997

Article

Year

Lifetime requirement of the methionine cycle for neuronal development and maintenance.

Current opinion in psychiatry, 2014, Volume: 27, Issue:2

Topics: Developmental Disabilities; Female; Folic Acid; Homocysteine; Humans; Methionine; Pregnancy; Prenatal Care; S-Adenosylmethionine; Vitamin B 12; Vitamin B Complex

2014

Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.

American journal of medical genetics, 1997, Sep-05, Volume: 71, Issue:4

Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Macrocytic; Anemia, Megaloblastic; Anorexia; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Genetic Complementation Test; Homocystine; Homocystinuria; Humans; Male; Methionine; Skin; Vitamin B 12

1997

Other Studies

11 other study(ies) available for methionine and Developmental Disabilities

Article	Year
Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits. Molecular psychiatry, 2018, Volume: 23, Issue:2 Topics: Animals; Antipsychotic Agents; Basic Helix-Loop-Helix Transcription Factors; CA1 Region, Hippocampal; Clozapine; Developmental Disabilities; Disease Models, Animal; Female; Folic Acid; Haloperidol; Humans; Male; Methionine; Mice; Neurogenesis; Neuronal Plasticity; One-Carbon Group Transferases; Prefrontal Cortex; Pregnancy; Prenatal Exposure Delayed Effects; Schizophrenia; Stereotyped Behavior; Tetrahydrofolates	2018
Severe methylenetetrahydrofolate reductase (MTHFR) deficiency: a case report of nonclassical homocystinuria. Journal of child neurology, 2008, Volume: 23, Issue:7 Topics: Child; Developmental Disabilities; Female; Homocysteine; Homocystinuria; Humans; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Severity of Illness Index; Vitamin B 12	2008
One-carbon metabolism-genome interactions in folate-associated pathologies. The Journal of nutrition, 2009, Volume: 139, Issue:12 Topics: Animals; Carbon; Child; Developmental Disabilities; Disease Models, Animal; Environment; Folic Acid; Gastrointestinal Neoplasms; Genetic Phenomena; Genome, Human; Homocysteine; Humans; Methionine; Mice; Neural Tube Defects; Purines; Risk Factors; Thymidine Monophosphate	2009
Reevaluation of a case of type 1 diabetes mellitus diagnosed before 6 months of age. Nature reviews. Endocrinology, 2010, Volume: 6, Issue:6 Topics: Administration, Oral; Adolescent; Amino Acid Substitution; Developmental Disabilities; Diabetes Mellitus, Type 1; Dose-Response Relationship, Drug; Epilepsy; Female; Glyburide; Glycated Hemoglobin; Humans; Hypoglycemic Agents; Infant; Methionine; Mutation; Potassium Channels, Inwardly Rectifying; Syndrome; Valine	2010
Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function. American journal of human genetics, 2011, Oct-07, Volume: 89, Issue:4 Topics: Adenosine Kinase; Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases; Child; Developmental Disabilities; Family Health; Female; Fibroblasts; Homocysteine; Humans; Liver Diseases; Male; Methionine; S-Adenosylhomocysteine; S-Adenosylmethionine	2011
Filamin a, periventricular nodular heterotopia, and West syndrome. Epilepsia, 2006, Volume: 47, Issue:6 Topics: Brain Diseases; Cerebral Ventricles; Choristoma; Contractile Proteins; Developmental Disabilities; Electroencephalography; Exons; Female; Filamins; Genetic Diseases, X-Linked; Humans; Infant; Male; Methionine; Microfilament Proteins; Mutation; Mutation, Missense; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Sequence Analysis, Protein; Spasms, Infantile; Threonine	2006
Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome. Human brain mapping, 2007, Volume: 28, Issue:6 Topics: Adolescent; Adult; Brain Mapping; Case-Control Studies; Catechol O-Methyltransferase; Cerebral Cortex; Chromosome Deletion; Chromosomes, Human, Pair 22; Developmental Disabilities; Female; Humans; Image Processing, Computer-Assisted; Inhibition, Psychological; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Oxygen; Schizophrenia; Valine	2007
Prenatal and postnatal presentation of severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) due to the FGFR3 Lys650Met mutation. American journal of medical genetics. Part A, 2008, Jan-15, Volume: 146A, Issue:2 Topics: Acanthosis Nigricans; Achondroplasia; Amino Acid Substitution; Developmental Disabilities; Female; Fetus; Humans; Infant, Newborn; Lysine; Male; Methionine; Mutation, Missense; Pregnancy; Receptor, Fibroblast Growth Factor, Type 3; Ultrasonography, Prenatal	2008
Short-term response to dietary therapy in molybdenum cofactor deficiency. Annals of neurology, 1993, Volume: 34, Issue:5 Topics: Acidosis, Lactic; Coenzymes; Cysteine; Developmental Disabilities; Female; Food, Fortified; Humans; Infant; Lactates; Metabolism, Inborn Errors; Metalloproteins; Methionine; Microcephaly; Molybdenum Cofactors; Pteridines	1993
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3. American journal of medical genetics, 1999, Jul-02, Volume: 85, Issue:1 Topics: Acanthosis Nigricans; Developmental Disabilities; Female; Humans; Infant, Newborn; Lysine; Male; Methionine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Skull	1999
Recombinant human growth hormone. Clinics in endocrinology and metabolism, 1986, Volume: 15, Issue:3 Topics: Alkaline Phosphatase; Amino Acid Sequence; Amino Acids; Base Sequence; Child; Cross Reactions; Developmental Disabilities; DNA; Growth Hormone; Human Growth Hormone; Humans; Macromolecular Substances; Methionine; Molecular Weight; Plasmids; Protein Conformation; Receptors, Somatotropin; Recombinant Proteins; Somatomedins	1986