103 related articles for article (PubMed ID: 1158480)
21. [Strychnine in non-ketotic hyperglycinemia].
Arenz B; Rister M; Sanchez A
Monatsschr Kinderheilkd; 1982 Aug; 130(8):621-3. PubMed ID: 7133018
[No Abstract] [Full Text] [Related]
22. [Non-ketotic hyperglycinemia. Study of a case].
Moura-Ribeiro MV; Ferlin ML; Gallina RA; Funayama CA; Fernandes RM
Arq Neuropsiquiatr; 1987 Mar; 45(1):67-71. PubMed ID: 3606438
[TBL] [Abstract][Full Text] [Related]
23. [Non-ketotic hyperglycinemia: clinical and therapeutic course in three patients].
Rite Gracia S; Guallarte Alias MP; Martínez Moral M; Baldellou Vázquez A; Rite Montañés S; Ruiz-Echarri Zalaya MP; Marco Tello A; Rebage Moisés V
An Esp Pediatr; 1999 Apr; 50(4):408-10. PubMed ID: 10356838
[No Abstract] [Full Text] [Related]
24. [Nonketone hyperglycinemia].
Wendt L; Similä S; Kouvalainen K
Pediatriia; 1981 May; (5):36-9. PubMed ID: 7279501
[No Abstract] [Full Text] [Related]
25. Familial neuromuscular disease with nonketotic hyperglycinemia.
Bank WJ; Morrow G
Trans Am Neurol Assoc; 1971; 96():21-3. PubMed ID: 5159084
[No Abstract] [Full Text] [Related]
26. [Hyperglycinemia in clinical-laboratory practice].
Ciani F; Pasquini E; Ciardetti A; Donati MA; Zammarchi E
Pediatr Med Chir; 1997; 19(2):109-12. PubMed ID: 9312744
[TBL] [Abstract][Full Text] [Related]
27. Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia.
Van Hove JL; Kishnani P; Muenzer J; Wenstrup RJ; Summar ML; Brummond MR; Lachiewicz AM; Millington DS; Kahler SG
Am J Med Genet; 1995 Dec; 59(4):444-53. PubMed ID: 8585564
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [Glycinosis (hyperglycinemia)].
Broyer M; Berger R
Presse Med (1893); 1968 Nov; 76(45):2155-6. PubMed ID: 5720120
[No Abstract] [Full Text] [Related]
30. Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.
Keating JP; Feigin RD; Tenenbaum SM; Hillman RE
Pediatrics; 1972 Dec; 50(6):890-5. PubMed ID: 4636454
[No Abstract] [Full Text] [Related]
31. The clinical findings in a patient with nonketotic hyperglycinemia.
Ziter FA; Bray PF; Madsen JA; Nyhan WL
Pediatr Res; 1968 Jul; 2(4):250-3. PubMed ID: 5691357
[No Abstract] [Full Text] [Related]
32. Nonketotic hyperglycinemia in a newborn infant.
Tekinalp G; Coşkun T; Oran O; Ozalp I; Figen G; Ergin H
Turk J Pediatr; 1995; 37(1):57-60. PubMed ID: 7732609
[TBL] [Abstract][Full Text] [Related]
33. Atypical non-ketotic hyperglycinaemia.
Borrone C; Bachmann C; Di Rocco M; Tada K; Hayasaka K; Gatti R
J Inherit Metab Dis; 1986; 9(4):402-3. PubMed ID: 3104680
[No Abstract] [Full Text] [Related]
34. Non-ketotic hyperglycinaemia: prenatal diagnosis and detection of heterozygotes with glycine/serine ratios.
Jordá A; Portolés M; Bonilla-Musoles F; Sweetman L; Nyhan WL
J Inherit Metab Dis; 1987; 10(2):198-9. PubMed ID: 3116341
[No Abstract] [Full Text] [Related]
35. Nystagmus and subnormal electroretinographic response in nonketotic hyperglycinemia.
Hayasaka S; Setogawa T; Hara S; Ishizawa S; Hayasaka K; Tada K
Graefes Arch Clin Exp Ophthalmol; 1987; 225(4):277-8. PubMed ID: 3653722
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Genomic analysis of non-ketotic hyperglycinaemia: a partial deletion of P-protein gene.
Tada K; Kure S; Kume A; Hiraga K
J Inherit Metab Dis; 1990; 13(5):766-70. PubMed ID: 2246863
[No Abstract] [Full Text] [Related]
38. Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.
Brandt IK; Hsia YE; Clement DH; Provence SA
Pediatrics; 1974 Mar; 53(3):391-5. PubMed ID: 4815259
[No Abstract] [Full Text] [Related]
39. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
Raven EJ
Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645
[No Abstract] [Full Text] [Related]
40. Spongy encephalopathy in ketotic hyperglycinemia.
Prosenc N; Stoltenburg-Didinger G
Brain Dev; 1994; 16(6):445-9. PubMed ID: 7694992
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
