pteridines has been researched along with Deficiency, Mental in 6 studies
Excerpt | Relevance | Reference |
---|---|---|
"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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (83.33) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aziz, AA | 1 |
Blair, JA | 1 |
Leeming, RJ | 1 |
Sylvester, PE | 1 |
Johnson, JL | 1 |
Waud, WR | 1 |
Rajagopalan, KV | 1 |
Duran, M | 1 |
Beemer, FA | 1 |
Wadman, SK | 1 |
Komada, S | 1 |
Masuzugawa, S | 1 |
Taniguchi, A | 1 |
Narita, Y | 1 |
Kuzuhara, S | 1 |
Aukett, A | 1 |
Bennett, MJ | 1 |
Hosking, GP | 1 |
Sahota, A | 1 |
Leeming, R | 1 |
Blair, J | 1 |
Hagberg, B | 1 |
Frézal, J | 1 |
6 other studies available for pteridines and Deficiency, Mental
Article | Year |
---|---|
Tetrahydrobiopterin metabolism in Down's syndrome and in non-Down's syndrome mental retardation.
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.
Topics: Child, Preschool; Coenzymes; Female; Fibroblasts; Humans; Immunologic Techniques; Intellectual Disab | 1980 |
[A case report of mild from of phenylketonuria].
Topics: Adult; Biomarkers; Humans; Intellectual Disability; Male; Phenylalanine; Phenylketonurias; Pteridine | 1996 |
Molybdenum co-factor deficiency: an easily missed inborn error of metabolism.
Topics: Aldehyde Oxidase; Aldehyde Oxidoreductases; Chromosome Aberrations; Chromosome Disorders; Coenzymes; | 1988 |
Tetrahydrobiopterin metabolism in the Rett disease.
Topics: Biopterins; Child; Dihydropteridine Reductase; Female; Humans; Intellectual Disability; NADH, NADPH | 1985 |
Medical physiopathology, enzymology and diagnosis.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Homocystinuria; Humans; Intellectual Disability; Mapl | 1972 |