Rüdel R - Search Results

1

Overexcited or inactive: ion channels in muscle disease.

Hoffman EP, Lehmann-Horn F, Rüdel R. Hoffman EP, et al. Among authors: rudel r. Cell. 1995 Mar 10;80(5):681-6. doi: 10.1016/0092-8674(95)90345-3. Cell. 1995. PMID: 7534212 Free article. Review. No abstract available.

2

Novel CLCN1 mutations with unique clinical and electrophysiological consequences.

Wu FF, Ryan A, Devaney J, Warnstedt M, Korade-Mirnics Z, Poser B, Escriva MJ, Pegoraro E, Yee AS, Felice KJ, Giuliani MJ, Mayer RF, Mongini T, Palmucci L, Marino M, Rüdel R, Hoffman EP, Fahlke C. Wu FF, et al. Among authors: rudel r. Brain. 2002 Nov;125(Pt 11):2392-407. doi: 10.1093/brain/awf246. Brain. 2002. PMID: 12390967

3

Molecular pathophysiology of voltage-gated ion channels.

Lehmann-Horn F, Rüdel R. Lehmann-Horn F, et al. Among authors: rudel r. Rev Physiol Biochem Pharmacol. 1996;128:195-268. doi: 10.1007/3-540-61343-9_9. Rev Physiol Biochem Pharmacol. 1996. PMID: 8791722 Review. No abstract available.

4

Genotype-phenotype correlations in human skeletal muscle sodium channel diseases.

Rüdel R, Ricker K, Lehmann-Horn F. Rüdel R, et al. Arch Neurol. 1993 Nov;50(11):1241-8. doi: 10.1001/archneur.1993.00540110113011. Arch Neurol. 1993. PMID: 8215982 Review.

5

Hereditary nondystrophic myotonias and periodic paralyses.

Lehmann-Horn F, Rüdel R. Lehmann-Horn F, et al. Among authors: rudel r. Curr Opin Neurol. 1995 Oct;8(5):402-10. doi: 10.1097/00019052-199510000-00014. Curr Opin Neurol. 1995. PMID: 8542048 Review.

6

Channelopathies: the nondystrophic myotonias and periodic paralyses.

Lehmann-Horn F, Rüdel R. Lehmann-Horn F, et al. Among authors: rudel r. Semin Pediatr Neurol. 1996 Jun;3(2):122-39. doi: 10.1016/s1071-9091(96)80041-6. Semin Pediatr Neurol. 1996. PMID: 8795846 Review.

7

Paramyotonia, potassium-aggravated myotonias and periodic paralyses. 37th ENMC International Workshop, Naarden, The Netherlands, 8-10 December 1995.

Rüdel R, Lehmann-Horn F. Rüdel R, et al. Neuromuscul Disord. 1997 Mar;7(2):127-32. doi: 10.1016/s0960-8966(96)00418-x. Neuromuscul Disord. 1997. PMID: 9131654 No abstract available.

8

Mutant channels contribute <50% to Na+ current in paramyotonia congenita muscle.

Mitrovic N, George AL Jr, Rüdel R, Lehmann-Horn F, Lerche H. Mitrovic N, et al. Among authors: rudel r. Brain. 1999 Jun;122 ( Pt 6):1085-92. doi: 10.1093/brain/122.6.1085. Brain. 1999. PMID: 10356061

9

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

Koch MC, Ricker K, Otto M, Grimm T, Bender K, Zoll B, Harper PS, Lehmann-Horn F, Rüdel R, Hoffman EP. Koch MC, et al. Among authors: rudel r. Hum Genet. 1991 Nov;88(1):71-4. doi: 10.1007/BF00204932. Hum Genet. 1991. PMID: 1660029

10

Non-dystrophic myotonias and periodic paralyses. A European Neuromuscular Center Workshop held 4-6 October 1992, Ulm, Germany.

Lehmann-Horn F, Rüdel R, Ricker K. Lehmann-Horn F, et al. Among authors: rudel r. Neuromuscul Disord. 1993 Mar;3(2):161-8. doi: 10.1016/0960-8966(93)90009-9. Neuromuscul Disord. 1993. PMID: 7689382 No abstract available.

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