201 related articles for article (PubMed ID: 15016427)
1. Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiency.
Surendran S; Ezell EL; Quast MJ; Wei J; Tyring SK; Michals-Matalon K; Matalon R
Neurosci Lett; 2004 Mar; 358(1):29-32. PubMed ID: 15016427
[TBL] [Abstract][Full Text] [Related]
2. Seizure evolution and amino acid imbalances in murine succinate semialdehyde dehydrogenase (SSADH) deficiency.
Gupta M; Polinsky M; Senephansiri H; Snead OC; Jansen EE; Jakobs C; Gibson KM
Neurobiol Dis; 2004 Aug; 16(3):556-62. PubMed ID: 15262267
[TBL] [Abstract][Full Text] [Related]
3. Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency.
Gropman A
Ann Neurol; 2003; 54 Suppl 6():S66-72. PubMed ID: 12891656
[TBL] [Abstract][Full Text] [Related]
4. Absence seizures in succinic semialdehyde dehydrogenase deficient mice: a model of juvenile absence epilepsy.
Cortez MA; Wu Y; Gibson KM; Snead OC
Pharmacol Biochem Behav; 2004 Nov; 79(3):547-53. PubMed ID: 15582027
[TBL] [Abstract][Full Text] [Related]
5. Murine succinate semialdehyde dehydrogenase deficiency.
Gupta M; Hogema BM; Grompe M; Bottiglieri TG; Concas A; Biggio G; Sogliano C; Rigamonti AE; Pearl PL; Snead OC; Jakobs C; Gibson KM
Ann Neurol; 2003; 54 Suppl 6():S81-90. PubMed ID: 12891658
[TBL] [Abstract][Full Text] [Related]
6. Succinic semialdehyde dehydrogenase deficiency: GABAB receptor-mediated function.
Buzzi A; Wu Y; Frantseva MV; Perez Velazquez JL; Cortez MA; Liu CC; Shen LQ; Gibson KM; Snead OC
Brain Res; 2006 May; 1090(1):15-22. PubMed ID: 16647690
[TBL] [Abstract][Full Text] [Related]
7. Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous system.
Matalon R; Rady PL; Platt KA; Skinner HB; Quast MJ; Campbell GA; Matalon K; Ceci JD; Tyring SK; Nehls M; Surendran S; Wei J; Ezell EL; Szucs S
J Gene Med; 2000; 2(3):165-75. PubMed ID: 10894262
[TBL] [Abstract][Full Text] [Related]
8. Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase.
Hogema BM; Gupta M; Senephansiri H; Burlingame TG; Taylor M; Jakobs C; Schutgens RB; Froestl W; Snead OC; Diaz-Arrastia R; Bottiglieri T; Grompe M; Gibson KM
Nat Genet; 2001 Oct; 29(2):212-6. PubMed ID: 11544478
[TBL] [Abstract][Full Text] [Related]
9. Expression of glutamate transporter, GABRA6, serine proteinase inhibitor 2 and low levels of glutamate and GABA in the brain of knock-out mouse for Canavan disease.
Surendran S; Rady PL; Michals-Matalon K; Quast MJ; Rassin DK; Campbell GA; Ezell EL; Wei J; Tyring SK; Szucs S; Matalon R
Brain Res Bull; 2003 Aug; 61(4):427-35. PubMed ID: 12909286
[TBL] [Abstract][Full Text] [Related]
10. Aspartoacylase gene knockout in the mouse: impact on reproduction.
Surendran S; Szucs S; Tyring SK; Matalon R
Reprod Toxicol; 2005; 20(2):281-3. PubMed ID: 15907664
[TBL] [Abstract][Full Text] [Related]
11. Canavan disease: studies on the knockout mouse.
Matalon R; Michals-Matalon K; Surendran S; Tyring SK
Adv Exp Med Biol; 2006; 576():77-93; discussion 361-3. PubMed ID: 16802706
[TBL] [Abstract][Full Text] [Related]
12. Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice).
Sauer SW; Kölker S; Hoffmann GF; Ten Brink HJ; Jakobs C; Gibson KM; Okun JG
Neurochem Int; 2007 Mar; 50(4):653-9. PubMed ID: 17303287
[TBL] [Abstract][Full Text] [Related]
13. Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency.
Dervent A; Gibson KM; Pearl PL; Salomons GS; Jakobs C; Yalcinkaya C
Clin Neurophysiol; 2004 Jun; 115(6):1417-22. PubMed ID: 15134710
[TBL] [Abstract][Full Text] [Related]
14. A mutation of aspartoacylase gene in a Turkish patient with Canavan disease.
Eke GH; Iscan A; Cece H; Calik M
Genet Couns; 2012; 23(1):9-12. PubMed ID: 22611636
[TBL] [Abstract][Full Text] [Related]
15. Succinic semialdehyde dehydrogenase deficiency (SSADH) (4-hydroxybutyric aciduria, gamma-hydroxybutyric aciduria).
Gordon N
Eur J Paediatr Neurol; 2004; 8(5):261-5. PubMed ID: 15341910
[TBL] [Abstract][Full Text] [Related]
16. Mouse neural progenitor cells differentiate into oligodendrocytes in the brain of a knockout mouse model of Canavan disease.
Surendran S; Shihabuddin LS; Clarke J; Taksir TV; Stewart GR; Parsons G; Yang W; Tyring SK; Michals-Matalon K; Matalon R
Brain Res Dev Brain Res; 2004 Oct; 153(1):19-27. PubMed ID: 15464214
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse.
Surendran S; Campbell GA; Tyring SK; Matalon R
Neurobiol Dis; 2005 Mar; 18(2):385-9. PubMed ID: 15686967
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Selective involvement of the globus pallidus and dentate nucleus in succinic semialdehyde dehydrogenase deficiency.
Ziyeh S; Berlis A; Korinthenberg R; Spreer J; Schumacher M
Pediatr Radiol; 2002 Aug; 32(8):598-600. PubMed ID: 12136353
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
