Gu W - Search Results

1

A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely.

Gu W, Bertrand D, Steinlein OK. Gu W, et al. Neurosci Lett. 2007 Jul 5;422(1):74-6. doi: 10.1016/j.neulet.2007.06.006. Epub 2007 Jun 8. Neurosci Lett. 2007. PMID: 17602836

2

The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins.

Gu W, Wevers A, Schröder H, Grzeschik KH, Derst C, Brodtkorb E, de Vos R, Steinlein OK. Gu W, et al. FEBS Lett. 2002 May 22;519(1-3):71-6. doi: 10.1016/s0014-5793(02)02713-8. FEBS Lett. 2002. PMID: 12023020 Free article.

3

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.

Gu W, Brodtkorb E, Steinlein OK. Gu W, et al. Ann Neurol. 2002 Sep;52(3):364-7. doi: 10.1002/ana.10280. Ann Neurol. 2002. PMID: 12205652

4

LGI1: a gene involved in epileptogenesis and glioma progression?

Gu W, Brodtkorb E, Piepoli T, Finocchiaro G, Steinlein OK. Gu W, et al. Neurogenetics. 2005 May;6(2):59-66. doi: 10.1007/s10048-005-0216-5. Epub 2005 Apr 13. Neurogenetics. 2005. PMID: 15827762 Review.

5

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.

Kananura C, Haug K, Sander T, Runge U, Gu W, Hallmann K, Rebstock J, Heils A, Steinlein OK. Kananura C, et al. Among authors: gu w. Arch Neurol. 2002 Jul;59(7):1137-41. doi: 10.1001/archneur.59.7.1137. Arch Neurol. 2002. PMID: 12117362

6

Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsy.

Gu W, Sander T, Becker T, Steinlein OK. Gu W, et al. Neurogenetics. 2004 Feb;5(1):41-4. doi: 10.1007/s10048-003-0158-8. Epub 2003 Sep 19. Neurogenetics. 2004. PMID: 14505228

7

Using gene-history and expression analyses to assess the involvement of LGI genes in human disorders.

Gu W, Gibert Y, Wirth T, Elischer A, Bloch W, Meyer A, Steinlein OK, Begemann G. Gu W, et al. Mol Biol Evol. 2005 Nov;22(11):2209-16. doi: 10.1093/molbev/msi214. Epub 2005 Jul 13. Mol Biol Evol. 2005. PMID: 16014869

8

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK. Gu W, et al. Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8. doi: 10.1016/j.eplepsyres.2005.07.003. Epilepsy Res. 2005. PMID: 16112844

9

Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore.

Hoda JC, Gu W, Friedli M, Phillips HA, Bertrand S, Antonarakis SE, Goudie D, Roberts R, Scheffer IE, Marini C, Patel J, Berkovic SF, Mulley JC, Steinlein OK, Bertrand D. Hoda JC, et al. Among authors: gu w. Mol Pharmacol. 2008 Aug;74(2):379-91. doi: 10.1124/mol.107.044545. Epub 2008 May 2. Mol Pharmacol. 2008. PMID: 18456869

10

Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation.

Brodtkorb E, Michler RP, Gu W, Steinlein OK. Brodtkorb E, et al. Among authors: gu w. Epilepsia. 2005 Jun;46(6):963-6. doi: 10.1111/j.1528-1167.2005.47104.x. Epilepsia. 2005. PMID: 15946341 Free article.

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