These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
136 related articles for article (PubMed ID: 5383004)
1. [Chromatographic studies in a family group with abnormalities of urea metabolism]. Colucci D'Amato F Osp Psichiatr; 1969; 37(3):363-9. PubMed ID: 5383004 [No Abstract] [Full Text] [Related]
2. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness. Sharp CW; Muir WJ; Blackwood DH; Walker M; Gosden C; St Clair DM Am J Med Genet; 1994 Dec; 54(4):354-60. PubMed ID: 7726208 [TBL] [Abstract][Full Text] [Related]
3. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation. Shih VE; Efron ML; Moser HW Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534 [No Abstract] [Full Text] [Related]
4. [Current problems of juvenile feeblemindedness]. Steinkopff E Z Arztl Fortbild (Jena); 1966 Sep; 60(17):989-94. PubMed ID: 4231816 [No Abstract] [Full Text] [Related]
5. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia. Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976 [No Abstract] [Full Text] [Related]
6. Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis. Scott-Emuakpor A; Higgins JV; Kohrman AF Pediatr Res; 1972 Jul; 6(7):626-33. PubMed ID: 5057291 [No Abstract] [Full Text] [Related]
8. [Hyperornithinemia, hyperammonemia and homocitrullinuria syndrome in a family]. Koike R; Fujimori K; Yuasa T; Miyatake T Rinsho Shinkeigaku; 1987 Apr; 27(4):465-71. PubMed ID: 3621746 [No Abstract] [Full Text] [Related]
9. Progressive quadriparesis, mental retardation, retinitis pigmentosa, and hearing loss: report of two sibs. Gordon AM; Capute AJ; Konigsmark BW Johns Hopkins Med J; 1976 Apr; 138(4):142-5. PubMed ID: 1271602 [TBL] [Abstract][Full Text] [Related]
10. [Changes in metabolism of tryptophan of a familial type with mental deficiency]. Giovannini M; Careddu P Pediatria (Napoli); 1967; 75(1):48-59. PubMed ID: 5601245 [No Abstract] [Full Text] [Related]
11. Carrier detection of urea cycle disorders. Ng WG; Oizumi J; Koch R; Shaw KN; McLaren J; Donnel GN; Carter M Pediatrics; 1981 Sep; 68(3):448-52. PubMed ID: 7279481 [No Abstract] [Full Text] [Related]
12. [Citrullinemia]. Vidailhet M; Levin B; Dautrevaux M; Paysant P; Gelot S; Badonnel Y; Pierson M; Neimann N Arch Fr Pediatr; 1971 May; 28(5):521-32. PubMed ID: 5561754 [No Abstract] [Full Text] [Related]
13. [An unusual picture of pigmentary dermatologic disease associated with retinitis pigmentosa, cataract and congenital deafness, oligophrenia and cerebellar ataxia]. Scialdone D; Artifoni E G Ital Oftalmol; 1964; 17(1):49-60. PubMed ID: 5827882 [No Abstract] [Full Text] [Related]
14. Growth of establishes lymphocytes in selective media: application to studies of inborn metabolic errors and somatic mutations. Streeter S; Spector E; Bloom A Birth Defects Orig Artic Ser; 1973 Jan; 9(1):138-54. PubMed ID: 4347331 [No Abstract] [Full Text] [Related]
15. [Early diagnosis of hereditary metabolic disorders as an effective means of preventing nervous system diseases in children]. Barashnev IuI; Kozlova SI Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1470-4. PubMed ID: 4947459 [No Abstract] [Full Text] [Related]
17. A case of hyperlysinemia: biochemical and clinical observations. Armstrong MD; Robinow M Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933 [No Abstract] [Full Text] [Related]
18. Congenital disorders of the urea cycle and ammonia detoxication. Colombo JP Monogr Paediatr; 1971; 1():1-150. PubMed ID: 4946766 [No Abstract] [Full Text] [Related]