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5. Congenital lysinuria: a new inherited transport disorder of dibasic amino acids. Oyanagi K; Miura R; Yamanouchi T J Pediatr; 1970 Aug; 77(2):259-66. PubMed ID: 5431208 [No Abstract] [Full Text] [Related]
6. 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]
7. Hypervalinemia. A defect in valine transamination. Dancis J; Hutzler J; Tada K; Wada Y; Morikawa T; Arakawa T Pediatrics; 1967 Jun; 39(6):813-7. PubMed ID: 6067402 [No Abstract] [Full Text] [Related]
8. 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]
9. Salient features of histidinemia. Ghadimi H; Partington MW Am J Dis Child; 1967 Jan; 113(1):83-7. PubMed ID: 6015913 [No Abstract] [Full Text] [Related]
11. Hereditary disorders of amino acid metabolism associated with mental deficiency. Berry HK Ann N Y Acad Sci; 1969 Sep; 166(1):66-73. PubMed ID: 5262032 [No Abstract] [Full Text] [Related]
12. [Amino acid imbalance as a pathogenetic factor in mental retardation (author's transl)]. Fekete G Klin Wochenschr; 1974 May; 52(6):276-82. PubMed ID: 4408538 [No Abstract] [Full Text] [Related]
13. Screening for aminoacidurias in psychiatric inpatients. Gershon ES; Shader RI Arch Gen Psychiatry; 1969 Jul; 21(1):82-8. PubMed ID: 5793684 [No Abstract] [Full Text] [Related]
14. Neurometabolic disorders in infancy, childhood and adolescence. Hagberg B Acta Neurol Scand; 1967; 43(S31):13-19. PubMed ID: 5583240 [No Abstract] [Full Text] [Related]
15. Further studies on hyperlysinemia associated with retardation. Ghadimi H; Zischka R; Binnington VI Am J Dis Child; 1967 Jan; 113(1):146-51. PubMed ID: 6015892 [No Abstract] [Full Text] [Related]