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8. The first case of 4-hydroxybutyric aciduria in Japan. Ishiguro Y; Kajita M; Aoshima T; Watanabe K; Kimura M; Yamaguchi S Brain Dev; 2001 Mar; 23(2):128-30. PubMed ID: 11248463 [TBL] [Abstract][Full Text] [Related]
9. 4-Hydroxybutyric aciduria: a new inborn error of metabolism. III. Enzymology and inheritance. Gibson KM; Jansen I; Sweetman L; Nyhan WL; Rating D; Jakobs C; Divry P J Inherit Metab Dis; 1984; 7 Suppl 1():95-6. PubMed ID: 6434853 [No Abstract] [Full Text] [Related]
10. 4-Hydroxybutyric aciduria: further clinical heterogeneity in a new case. Onkenhout W; Maaswinkel-Mooij PD; Poorthuis BJ Eur J Pediatr; 1989 Dec; 149(3):194-6. PubMed ID: 2482184 [TBL] [Abstract][Full Text] [Related]
11. Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism. Jakobs C; Bojasch M; Mönch E; Rating D; Siemes H; Hanefeld F Clin Chim Acta; 1981 Apr; 111(2-3):169-78. PubMed ID: 7226548 [No Abstract] [Full Text] [Related]
12. 3-Methylglutaconic aciduria: ten new cases with a possible new phenotype. al Aqeel A; Rashed M; Ozand PT; Brismar J; Gascon GG; al Odaib A; Dabbagh O Brain Dev; 1994 Nov; 16 Suppl():23-32. PubMed ID: 7726378 [TBL] [Abstract][Full Text] [Related]
13. [Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]. Escalera GI; Ferrer I; Marina LC; Sala PR; Salomons GS; Jakobs C; Pérez-Cerdá C An Pediatr (Barc); 2010 Feb; 72(2):128-32. PubMed ID: 20018576 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. Vigabatrin for refractory partial seizures in children with tuberous sclerosis. Curatolo P Neuropediatrics; 1994 Feb; 25(1):55. PubMed ID: 8208356 [No Abstract] [Full Text] [Related]
16. 4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism. Gibson KM; Hoffmann GF; Hodson AK; Bottiglieri T; Jakobs C Neuropediatrics; 1998 Feb; 29(1):14-22. PubMed ID: 9553943 [TBL] [Abstract][Full Text] [Related]
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18. A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolism. Divry P; Baltassat P; Rolland MO; Cotte J; Hermier M; Duran M; Wadman SK Clin Chim Acta; 1983 Apr; 129(3):303-9. PubMed ID: 6133657 [No Abstract] [Full Text] [Related]
19. Management of West syndrome in a patient with methylmalonic aciduria. Campeau PM; Valayannopoulos V; Touati G; Bahi-Buisson N; Boddaert N; Plouin P; Rabier D; Benoist JF; Dulac O; de Lonlay P; Desguerre I J Child Neurol; 2010 Jan; 25(1):94-7. PubMed ID: 19700743 [TBL] [Abstract][Full Text] [Related]