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24. Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency. Gibson KM; DeVivo DC; Jakobs C Lancet; 1989 Nov; 2(8671):1105-6. PubMed ID: 2572834 [No Abstract] [Full Text] [Related]
25. Succinic semialdehyde dehydrogenase deficiency in siblings: clinical heterogeneity and response to early treatment. Peters H; Cleary M; Boneh A J Inherit Metab Dis; 1999 Apr; 22(2):198-9. PubMed ID: 10234622 [No Abstract] [Full Text] [Related]
26. A unique mouse model for succinic semialdehyde dehydrogenase deficiency with implications for gamma hydroxybutyrate intoxication. Peters H Pharmacogenomics J; 2002; 2(1):3-4. PubMed ID: 11990378 [No Abstract] [Full Text] [Related]
28. Neurodevelopmental pattern of succinic semialdehyde dehydrogenase deficiency (gamma-hydroxybutyric aciduria). Philippe A; Deron J; Geneviève D; de Lonlay P; Gibson KM; Rabier D; Munnich A Dev Med Child Neurol; 2004 Aug; 46(8):564-8. PubMed ID: 15287248 [TBL] [Abstract][Full Text] [Related]
29. Therapeutic intervention in mice deficient for succinate semialdehyde dehydrogenase (gamma-hydroxybutyric aciduria). Gupta M; Greven R; Jansen EE; Jakobs C; Hogema BM; Froestl W; Snead OC; Bartels H; Grompe M; Gibson KM J Pharmacol Exp Ther; 2002 Jul; 302(1):180-7. PubMed ID: 12065715 [TBL] [Abstract][Full Text] [Related]
30. GABA, gamma-hydroxybutyric acid, and neurological disease. Wong CG; Bottiglieri T; Snead OC Ann Neurol; 2003; 54 Suppl 6():S3-12. PubMed ID: 12891648 [TBL] [Abstract][Full Text] [Related]
31. Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria). Chambliss KL; Hinson DD; Trettel F; Malaspina P; Novelletto A; Jakobs C; Gibson KM Am J Hum Genet; 1998 Aug; 63(2):399-408. PubMed ID: 9683595 [TBL] [Abstract][Full Text] [Related]
32. The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family. Bekri S; Fossoud C; Plaza G; Guenne A; Salomons GS; Jakobs C; Van Obberghen E Mol Genet Metab; 2004 Apr; 81(4):347-51. PubMed ID: 15059623 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. Succinic semialdehyde dehydrogenase deficiency in children and adults. Pearl PL; Novotny EJ; Acosta MT; Jakobs C; Gibson KM Ann Neurol; 2003; 54 Suppl 6():S73-80. PubMed ID: 12891657 [TBL] [Abstract][Full Text] [Related]
36. [Prenatal diagnosis of congenital diseases by means of the biochemical study of the amniotic fluid obtained in the 16th week of pregnancy]. Lato M; Rufini S; Lungarotti MS; Valenti C; Ghebregzabher M; Monaldi B Minerva Ginecol; 1976; 28(7-8):589-95. PubMed ID: 65748 [No Abstract] [Full Text] [Related]