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42. Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia. Kure S; Takayanagi M; Narisawa K; Tada K; Leisti J J Clin Invest; 1992 Jul; 90(1):160-4. PubMed ID: 1634607 [TBL] [Abstract][Full Text] [Related]
43. Metabolism of glycine in the nonketotic form of hyperglycinemia. Ando T; Nyhan WL; Gerritsen T; Gong L; Heiner DC; Bray PF Pediatr Res; 1968 Jul; 2(4):254-63. PubMed ID: 5669662 [No Abstract] [Full Text] [Related]
44. Depletion of cerebral D-serine in non-ketotic hyperglycinemia: possible involvement of glycine cleavage system in control of endogenous D-serine. Iwama H; Takahashi K; Kure S; Hayashi F; Narisawa K; Tada K; Mizoguchi M; Takashima S; Tomita U; Nishikawa T Biochem Biophys Res Commun; 1997 Feb; 231(3):793-6. PubMed ID: 9070895 [TBL] [Abstract][Full Text] [Related]
46. Hyperglycinuria and hyperglycinemia in two siblings with mild developmental delays. Frazier DM; Summer GK; Chamberlin HR Am J Dis Child; 1978 Aug; 132(8):777-81. PubMed ID: 80128 [TBL] [Abstract][Full Text] [Related]
47. [Clinical findings and therapeutic problems in nonketotic hyperglycinemia]. Koepp P; de Groot CJ; Grüttner R; Rybak FC Monatsschr Kinderheilkd (1902); 1973 Jul; 121(7):401-3. PubMed ID: 4751474 [No Abstract] [Full Text] [Related]
48. Non-ketotic hyperglycinemia (NKH): an inborn error of metabolism affecting brain function exclusively. de Groot CJ; Boeli Everts V; Touwen BC; Hommes FA Prog Brain Res; 1978; 48():199-207. PubMed ID: 746154 [No Abstract] [Full Text] [Related]
49. Nonketotic hyperglycinemia. A genetic study of 13 Finnish families. von Wendt L; Hirvasniemi A; Similä S Clin Genet; 1979 May; 15(5):411-7. PubMed ID: 445864 [TBL] [Abstract][Full Text] [Related]
50. Failure of early dextromethorphan and sodium benzoate therapy in an infant with nonketotic hyperglycinemia. Zammarchi E; Donati MA; Ciani F; Pasquini E; Pela I; Fiorini P Neuropediatrics; 1994 Oct; 25(5):274-6. PubMed ID: 7885541 [TBL] [Abstract][Full Text] [Related]
51. Problems of prenatal diagnosis of non-ketotic hyperglycinaemia. von Wendt L; Similä S; Ruokonen A; Hartikainen-Sorri AL J Inherit Metab Dis; 1983; 6(3):112-3. PubMed ID: 6422141 [TBL] [Abstract][Full Text] [Related]
52. Neurologic sequelae in transient nonketotic hyperglycinemia of the neonate. Eyskens FJ; Van Doorn JW; Mariën P J Pediatr; 1992 Oct; 121(4):620-1. PubMed ID: 1403401 [TBL] [Abstract][Full Text] [Related]
53. Use of placental enzyme analysis in assessment of the newborn at risk for non-ketotic hyperglycinaemia (NKH). Toone JR; Applegarth DA J Inherit Metab Dis; 1989; 12(3):281-5. PubMed ID: 2515368 [TBL] [Abstract][Full Text] [Related]
54. The neuropathology of the nonketotic and ketotic hyperglycinemias: three cases. Shuman RM; Leech RW; Scott CR Neurology; 1978 Feb; 28(2):139-46. PubMed ID: 563996 [TBL] [Abstract][Full Text] [Related]
55. [Etiologic analysis of familial hyperglycinemia and its application in prenatal diagnosis]. Tada K Nihon Rinsho; 1988 Aug; 46(8):1865-77. PubMed ID: 3070081 [No Abstract] [Full Text] [Related]
56. Propionic acidemia and anorectal anomalies in three siblings. Branski D; Gale R; Gross-Kieselstein E; Abrahamov A Am J Dis Child; 1977 Dec; 131(12):1379-81. PubMed ID: 930888 [TBL] [Abstract][Full Text] [Related]
57. Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia). Toone JR; Applegarth DA; Kure S; Coulter-Mackie MB; Sazegar P; Kojima K; Ichinohe A Mol Genet Metab; 2002 Jul; 76(3):243-9. PubMed ID: 12126939 [TBL] [Abstract][Full Text] [Related]