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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Haug K, Warnstedt M, Alekov AK, Sander T, Ramírez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H, Heils A. Haug K, et al. Among authors: lerche h. Nat Genet. 2003 Apr;33(4):527-32. doi: 10.1038/ng1121. Epub 2003 Mar 3. Nat Genet. 2003. PMID: 12612585 Retracted.
C-terminal interaction of KCNQ2 and KCNQ3 K+ channels.
Maljevic S, Lerche C, Seebohm G, Alekov AK, Busch AE, Lerche H. Maljevic S, et al. Among authors: lerche c, lerche h. J Physiol. 2003 Apr 15;548(Pt 2):353-60. doi: 10.1113/jphysiol.2003.040980. Epub 2003 Mar 14. J Physiol. 2003. PMID: 12640002 Free PMC article.
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study.
Kassubek J, Juengling FD, Hoffmann S, Rosenbohm A, Kurt A, Jurkat-Rott K, Steinbach P, Wolf M, Ludolph AC, Lehmann-Horn F, Lerche H, Weber YG. Kassubek J, et al. Among authors: lerche h. Neurosci Lett. 2003 Sep 11;348(2):73-6. doi: 10.1016/s0304-3940(03)00740-7. Neurosci Lett. 2003. PMID: 12902021
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. Among authors: lerche h. Epilepsia. 2004 Jun;45(6):601-9. doi: 10.1111/j.0013-9580.2004.48203.x. Epilepsia. 2004. PMID: 15144424 Free article.
Ion channel defects in idiopathic epilepsies.
Lerche H, Weber YG, Jurkat-Rott K, Lehmann-Horn F. Lerche H, et al. Curr Pharm Des. 2005;11(21):2737-52. doi: 10.2174/1381612054546815. Curr Pharm Des. 2005. PMID: 16101452 Review.
341 results