Weber YG - Search Results

1

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.

Gardella E, Becker F, Møller RS, Schubert J, Lemke JR, Larsen LH, Eiberg H, Nothnagel M, Thiele H, Altmüller J, Syrbe S, Merkenschlager A, Bast T, Steinhoff B, Nürnberg P, Mang Y, Bakke Møller L, Gellert P, Heron SE, Dibbens LM, Weckhuysen S, Dahl HA, Biskup S, Tommerup N, Hjalgrim H, Lerche H, Beniczky S, Weber YG. Gardella E, et al. Among authors: weber yg. Ann Neurol. 2016 Mar;79(3):428-36. doi: 10.1002/ana.24580. Epub 2016 Feb 13. Ann Neurol. 2016. PMID: 26677014

2

Generalized epilepsy with febrile seizures plus: further heterogeneity in a large family.

Lerche H, Weber YG, Baier H, Jurkat-Rott K, Kraus de Camargo O, Ludolph AC, Bode H, Lehmann-Horn F. Lerche H, et al. Among authors: weber yg. Neurology. 2001 Oct 9;57(7):1191-8. doi: 10.1212/wnl.57.7.1191. Neurology. 2001. PMID: 11591834

3

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.

Weber YG, Berger A, Bebek N, Maier S, Karafyllakes S, Meyer N, Fukuyama Y, Halbach A, Hikel C, Kurlemann G, Neubauer B, Osawa M, Püst B, Rating D, Saito K, Stephani U, Tauer U, Lehmann-Horn F, Jurkat-Rott K, Lerche H. Weber YG, et al. Epilepsia. 2004 Jun;45(6):601-9. doi: 10.1111/j.0013-9580.2004.48203.x. Epilepsia. 2004. PMID: 15144424 Free article.

4

Ion channel defects in idiopathic epilepsies.

Lerche H, Weber YG, Jurkat-Rott K, Lehmann-Horn F. Lerche H, et al. Among authors: weber yg. Curr Pharm Des. 2005;11(21):2737-52. doi: 10.2174/1381612054546815. Curr Pharm Des. 2005. PMID: 16101452 Review.

5

Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain.

Weber YG, Geiger J, Kämpchen K, Landwehrmeyer B, Sommer C, Lerche H. Weber YG, et al. Brain Res. 2006 Mar 10;1077(1):1-6. doi: 10.1016/j.brainres.2006.01.023. Epub 2006 Feb 28. Brain Res. 2006. PMID: 16500630

6

Epileptic nystagmus: two case reports, clinical and pathophysiological review of the literature.

Weber YG, Roesche J, Lerche H. Weber YG, et al. J Neurol. 2006 Jun;253(6):767-71. doi: 10.1007/s00415-006-0114-2. Epub 2006 Mar 6. J Neurol. 2006. PMID: 16511649 Review.

7

Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain.

Geiger J, Weber YG, Landwehrmeyer B, Sommer C, Lerche H. Geiger J, et al. Among authors: weber yg. Neurosci Lett. 2006 May 29;400(1-2):101-4. doi: 10.1016/j.neulet.2006.02.017. Epub 2006 Mar 2. Neurosci Lett. 2006. PMID: 16513263

8

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.

Maljevic S, Krampfl K, Cobilanschi J, Tilgen N, Beyer S, Weber YG, Schlesinger F, Ursu D, Melzer W, Cossette P, Bufler J, Lerche H, Heils A. Maljevic S, et al. Among authors: weber yg. Ann Neurol. 2006 Jun;59(6):983-7. doi: 10.1002/ana.20874. Ann Neurol. 2006. PMID: 16718694

9

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

Hempelmann A, Cobilanschi J, Heils A, Muhle H, Stephani U, Weber Y, Lerche H, Sander T. Hempelmann A, et al. Epilepsy Res. 2007 Apr;74(1):28-32. doi: 10.1016/j.eplepsyres.2006.12.001. Epub 2007 Jan 9. Epilepsy Res. 2007. PMID: 17215107

10

A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1.

Weber YG, Jacob M, Weber G, Lerche H. Weber YG, et al. Among authors: weber g. Epilepsia. 2008 Nov;49(11):1959-64. doi: 10.1111/j.1528-1167.2008.01646.x. Epub 2008 May 8. Epilepsia. 2008. PMID: 18479394 Free article.

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