137 related articles for article (PubMed ID: 3091926)
1. Non-ketotic hyperglycinaemia due to a deficiency of T-protein in the glycine cleavage system in liver and brain.
Schutgens RB; Ket JL; Hayasaka K; Tada K
J Inherit Metab Dis; 1986; 9(2):208-14. PubMed ID: 3091926
[TBL] [Abstract][Full Text] [Related]
2. Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect.
Haan EA; Kirby DM; Tada K; Hayasaka K; Danks DM
Eur J Pediatr; 1986 Sep; 145(4):267-70. PubMed ID: 3769993
[TBL] [Abstract][Full Text] [Related]
3. Nonketotic hyperglycinemia: two patients with primary defects of P-protein and T-protein, respectively, in the glycine cleavage system.
Hayasaka K; Tada K; Kikuchi G; Winter S; Nyhan WL
Pediatr Res; 1983 Dec; 17(12):967-70. PubMed ID: 6336599
[TBL] [Abstract][Full Text] [Related]
4. Molecular lesion of non-ketotic hyperglycinaemia.
Tada K; Hayasaka K
J Inherit Metab Dis; 1984; 7 Suppl 2():143-4. PubMed ID: 6434872
[No Abstract] [Full Text] [Related]
5. Defective glycine cleavage system in nonketotic hyperglycinemia. Occurrence of a less active glycine decarboxylase and an abnormal aminomethyl carrier protein.
Hiraga K; Kochi H; Hayasaka K; Kikuchi G; Nyhan WL
J Clin Invest; 1981 Aug; 68(2):525-34. PubMed ID: 6790577
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of non-ketotic hyperglycinaemia.
Toone JR; Applegarth DA; Levy HL
J Inherit Metab Dis; 1992; 15(5):713-9. PubMed ID: 1434509
[TBL] [Abstract][Full Text] [Related]
7. Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical cases.
Hayasaka K; Tada K; Fueki N; Nakamura Y; Nyhan WL; Schmidt K; Packman S; Seashore MR; Haan E; Danks DM
J Pediatr; 1987 Jun; 110(6):873-7. PubMed ID: 3585602
[TBL] [Abstract][Full Text] [Related]
8. First-trimester prenatal diagnosis of non-ketotic hyperglycinaemia by a micro assay of glycine cleavage enzyme.
Rolland MO; Mandon G; Mathieu M
Prenat Diagn; 1993 Aug; 13(8):771-2. PubMed ID: 8284296
[No Abstract] [Full Text] [Related]
9. Non-ketotic hyperglycinaemia: clinical and biochemical aspects.
Tada K; Hayasaka K
Eur J Pediatr; 1987 May; 146(3):221-7. PubMed ID: 3297708
[TBL] [Abstract][Full Text] [Related]
10. Strychnine therapy in nonketotic hyperglycinemia.
Arneson D; Ch'ien LT; Chance P; Wilroy RS
Pediatrics; 1979 Mar; 63(3):369-73. PubMed ID: 440838
[TBL] [Abstract][Full Text] [Related]
11. A strategy for glycine encephalopathy therapy.
Mendelson IS
J Ment Defic Res; 1982 Jun; 26 (Pt 2)():107-10. PubMed ID: 6809951
[TBL] [Abstract][Full Text] [Related]
12. Postnatal development of the glycine cleavage system in rat liver.
Kalbag SS; Palekar AG
Biochem Med Metab Biol; 1990 Apr; 43(2):128-32. PubMed ID: 2112009
[TBL] [Abstract][Full Text] [Related]
13. Some aspects of glycine neurochemistry.
Mayor F; Valdivieso F; Ugarte M; Benavides J; García ML; Lahoya JL; Mayor F
Adv Biochem Psychopharmacol; 1981; 29():551-60. PubMed ID: 6266229
[No Abstract] [Full Text] [Related]
14. Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).
Toone JR; Applegarth DA; Coulter-Mackie MB; James ER
Mol Genet Metab; 2001 Apr; 72(4):322-5. PubMed ID: 11286506
[TBL] [Abstract][Full Text] [Related]
15. Structure and chromosomal localization of the aminomethyltransferase gene (AMT).
Nanao K; Takada G; Takahashi E; Seki N; Komatsu Y; Okamura-Ikeda K; Motokawa Y; Hayasaka K
Genomics; 1994 Jan; 19(1):27-30. PubMed ID: 8188235
[TBL] [Abstract][Full Text] [Related]
16. Non-ketotic hyperglycinaemia in a neonate. A case report.
De Ravel TJ; Smith CE; Scher LG; Davies VA; Rothberg AD
S Afr Med J; 1991 Aug; 80(4):201-2. PubMed ID: 1876959
[TBL] [Abstract][Full Text] [Related]
17. Inhibition of glycine oxidation by pyruvate, alpha-ketoglutarate, and branched-chain alpha-keto acids in rat liver mitochondria: presence of interaction between the glycine cleavage system and alpha-keto acid dehydrogenase complexes.
Kochi H; Seino H; Ono K
Arch Biochem Biophys; 1986 Sep; 249(2):263-72. PubMed ID: 3753002
[TBL] [Abstract][Full Text] [Related]
18. Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemia.
Steinmann B; Gitzelmann R
Helv Paediatr Acta; 1979; 34(6):589-99. PubMed ID: 541222
[TBL] [Abstract][Full Text] [Related]
19. Glycine metabolism and glycine synthase activity during the postnatal development of rat brain.
Lahoya JL; Benavides J; Ugarte M
Dev Neurosci; 1980; 3(2):75-80. PubMed ID: 7418631
[TBL] [Abstract][Full Text] [Related]
20. Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH).
Toone JR; Applegarth DA; Levy HL; Coulter-Mackie MB; Lee G
Mol Genet Metab; 2003 Aug; 79(4):272-80. PubMed ID: 12948742
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
