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Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
Fan C, Wolking S, Lehmann-Horn F, Hedrich UB, Freilinger T, Lerche H, Borck G, Kubisch C, Jurkat-Rott K. Fan C, et al. Cephalalgia. 2016 Nov;36(13):1238-1247. doi: 10.1177/0333102415608360. Epub 2016 Jul 11. Cephalalgia. 2016. PMID: 26763045 Free PMC article.
Skeletal muscle channelopathies.
Jurkat-Rott K, Lerche H, Lehmann-Horn F. Jurkat-Rott K, et al. J Neurol. 2002 Nov;249(11):1493-502. doi: 10.1007/s00415-002-0871-5. J Neurol. 2002. PMID: 12420087 Review.
Teaching course: ion channelopathies in neurology.
Jurkat-Rott K, Lerche H, Mitrovic N, Lehmann-Horn F. Jurkat-Rott K, et al. J Neurol. 1999 Sep;246(9):758-63. doi: 10.1007/s004150050451. J Neurol. 1999. PMID: 10525971 Review. No abstract available.
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.
Hereditary channelopathies in neurology.
Jurkat-Rott K, Lerche H, Weber Y, Lehmann-Horn F. Jurkat-Rott K, et al. Adv Exp Med Biol. 2010;686:305-34. doi: 10.1007/978-90-481-9485-8_18. Adv Exp Med Biol. 2010. PMID: 20824453 Review.
131 results