homocysteine and Intellectual Disability

homocysteine has been researched along with Intellectual Disability in 17 studies

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-199013 (76.47)18.7374
1990's0 (0.00)18.2507
2000's4 (23.53)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chatterjee, A; Chattopadhyay, A; Dutta, S; Mukhopadhyay, K; Sinha, S1
Burlina, AB; Burlina, AP; Edini, C1
Bernardino, L; Brito, AP; Fonseca, N; InĂªs, L; Santos, J; Silvestre, I; Vidal, N1
CARSON, NA; CUSWORTH, DC; DENT, CE; FIELD, CM; NEILL, DW; WESTALL, RG1
COFFEY, VP1
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D1
BRENTON, DP; CUSWORTH, DC; GAULL, GE1
Hansen, S; MacDougall, L; Perry, TL; Warrington, PD1
Erbe, RW; Wang, JC1
Bassan, H; Fattal-Valevski, A; Gutman, A; Harel, S; Korman, SH; Lerman-Sagie, T1
Sviatkina, OB; Vel'tishchev, IuE1
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, IJ1
Schimke, RN; Spiro, HR; Welch, JP1
Araki, S; Cowen, D; Rowland, LP; Thompson, HL; White, HH1
Dolman, CL; Dunn, HG; Perry, TL1
Gaitonde, MK; Gaull, G1

Reviews

1 review(s) available for homocysteine and Intellectual Disability

ArticleYear
[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

Other Studies

16 other study(ies) available for homocysteine and Intellectual Disability

ArticleYear
Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata.
    Neuroscience letters, 2009, Apr-10, Volume: 453, Issue:3

    Topics: Adolescent; Adult; Case-Control Studies; Child; Child, Preschool; Cystathionine beta-Synthase; Female; Gene Frequency; Genotype; Haplotypes; Homocysteine; Humans; Intellectual Disability; Male; Polymorphism, Genetic; Sex Factors; White People; Young Adult

2009
Treatment of extrapyramidal symptoms in a patient with homozygous homocystinuria.
    Journal of inherited metabolic disease, 2002, Volume: 25, Issue:2

    Topics: Adult; Anticonvulsants; Clonazepam; Cystathionine beta-Synthase; Dystonia; Female; Homocysteine; Homocystinuria; Humans; Intellectual Disability

2002
Hyperhomocysteinemia--case report.
    Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology, 2003, Volume: 22, Issue:2

    Topics: Adult; Cerebrovascular Disorders; Exophthalmos; Female; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Intellectual Disability

2003
HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
    Archives of disease in childhood, 1963, Volume: 38

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Genetics, Medical; Homocysteine; Homocystinuria; Humans; Intellectual Disability; Kidney; Northern Ireland; Renal Aminoacidurias; Urologic Diseases

1963
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    Journal of the Irish Medical Association, 1964, Volume: 54

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency

1964
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    The New England journal of medicine, 1964, Jun-25, Volume: 270

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine

1964
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
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
Folate metabolism in humans.
    American journal of medical genetics, 1984, Volume: 17, Issue:1

    Topics: Amino Acids; Cells, Cultured; Chemical Phenomena; Chemistry; Culture Media; Folic Acid; Folic Acid Deficiency; Fragile X Syndrome; Histidine; Homocysteine; Humans; Intellectual Disability; Lymphocytes; Sex Chromosome Aberrations; Tetrahydrofolates

1984
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
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
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
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
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