Page last updated: 2024-10-20

pteridines and Deficiency, Mental

pteridines has been researched along with Deficiency, Mental in 6 studies

Research Excerpts

ExcerptRelevanceReference
"He showed mild mental retardation, and the WAIS was 46 in PIQ, 70 in VIQ and 53 in total IQ."1.29[A case report of mild from of phenylketonuria]. ( Komada, S; Kuzuhara, S; Masuzugawa, S; Narita, Y; Taniguchi, A, 1996)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aziz, AA1
Blair, JA1
Leeming, RJ1
Sylvester, PE1
Johnson, JL1
Waud, WR1
Rajagopalan, KV1
Duran, M1
Beemer, FA1
Wadman, SK1
Komada, S1
Masuzugawa, S1
Taniguchi, A1
Narita, Y1
Kuzuhara, S1
Aukett, A1
Bennett, MJ1
Hosking, GP1
Sahota, A1
Leeming, R1
Blair, J1
Hagberg, B1
Frézal, J1

Other Studies

6 other studies available for pteridines and Deficiency, Mental

ArticleYear
Tetrahydrobiopterin metabolism in Down's syndrome and in non-Down's syndrome mental retardation.
    Journal of mental deficiency research, 1982, Volume: 26 (Pt 2)

    Topics: Adult; Aged; Biopterins; Down Syndrome; Female; Humans; Intellectual Disability; Male; Middle Aged;

1982
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.
    Proceedings of the National Academy of Sciences of the United States of America, 1980, Volume: 77, Issue:6

    Topics: Child, Preschool; Coenzymes; Female; Fibroblasts; Humans; Immunologic Techniques; Intellectual Disab

1980
[A case report of mild from of phenylketonuria].
    Rinsho shinkeigaku = Clinical neurology, 1996, Volume: 36, Issue:5

    Topics: Adult; Biomarkers; Humans; Intellectual Disability; Male; Phenylalanine; Phenylketonurias; Pteridine

1996
Molybdenum co-factor deficiency: an easily missed inborn error of metabolism.
    Developmental medicine and child neurology, 1988, Volume: 30, Issue:4

    Topics: Aldehyde Oxidase; Aldehyde Oxidoreductases; Chromosome Aberrations; Chromosome Disorders; Coenzymes;

1988
Tetrahydrobiopterin metabolism in the Rett disease.
    Brain & development, 1985, Volume: 7, Issue:3

    Topics: Biopterins; Child; Dihydropteridine Reductase; Female; Humans; Intellectual Disability; NADH, NADPH

1985
Medical physiopathology, enzymology and diagnosis.
    Monographs in human genetics, 1972, Volume: 6

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Homocystinuria; Humans; Intellectual Disability; Mapl

1972