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6. Nonketotic hyperglycinaemia. Clinical findings and amino acid analyses on the plasma of a new case. Ferdinand W; Gordon RR; Owen G Clin Chim Acta; 1970 Dec; 30(3):745-9. PubMed ID: 5493897 [No Abstract] [Full Text] [Related]
7. Hyperprolinaemia in two successive generations of a North American Indian family. Perry TL; Hardwick DF; Lowry RB; Hansen S Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764 [No Abstract] [Full Text] [Related]
8. [Familial hyperprolinemia--a case in a family]. Oknińska A; Grygalewicz J; Kowalewska-Kantecka B; Iwańska J Pol Arch Med Wewn; 1974 Feb; 51(2):189-97. PubMed ID: 4816363 [No Abstract] [Full Text] [Related]
9. Letter: Homocarnosinosis: a new metabolic disorder associated with spasticity and mental retardation. Gjessing LR; Sjaastad O Lancet; 1974 Oct; 2(7887):1028. PubMed ID: 4138320 [No Abstract] [Full Text] [Related]
10. FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT. EFRON ML N Engl J Med; 1965 Jun; 272():1243-54. PubMed ID: 14290545 [No Abstract] [Full Text] [Related]
12. The clinical findings in a patient with nonketotic hyperglycinemia. Reploh H; Gröbe H; Diekmann L; Palm D; von Bassewitz DB; Jenett W Z Kinderheilkd; 1973; 114(3):191-204. PubMed ID: 4723704 [No Abstract] [Full Text] [Related]
19. MENTAL RETARDATION AND ABNORMAL AMINOACIDURIAS OCCURRING IN A FAMILY. ANYON CP N Z Med J; 1965 Jan; 64():3-7. PubMed ID: 14259628 [No Abstract] [Full Text] [Related]
20. Urinary aminoacids in mental retardation. Dhatt PS; Gupta HL; Saini AS Indian J Pediatr; 1968 Oct; 35(249):469-75. PubMed ID: 5719650 [No Abstract] [Full Text] [Related] [Next] [New Search]