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Page 1
Dysfunction of dysferlin-deficient hearts.
Wenzel K, Geier C, Qadri F, Hubner N, Schulz H, Erdmann B, Gross V, Bauer D, Dechend R, Dietz R, Osterziel KJ, Spuler S, Ozcelik C. Wenzel K, et al. Among authors: spuler s. J Mol Med (Berl). 2007 Nov;85(11):1203-14. doi: 10.1007/s00109-007-0253-7. Epub 2007 Sep 9. J Mol Med (Berl). 2007. PMID: 17828519
A new LMNA mutation causing limb girdle muscular dystrophy 1B.
Spuler S, Geier C, Osterziel KJ, Gutberlet M, Genschel J, Lehmann TN, Zinn-Justin S, Gilquin B, Schmidt H. Spuler S, et al. J Neurol. 2005 May;252(5):621-3. doi: 10.1007/s00415-005-0719-x. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789136 No abstract available.
[Cardiac manifestations of muscular dystrophies].
Perrot A, Spuler S, Geier C, Dietz R, Osterziel KJ. Perrot A, et al. Among authors: spuler s. Z Kardiol. 2005 May;94(5):312-20. doi: 10.1007/s00392-005-0232-3. Z Kardiol. 2005. PMID: 15868359 Review. German.
Muscle and nerve pathology in Dunnigan familial partial lipodystrophy.
Spuler S, Kalbhenn T, Zabojszcza J, van Landeghem FK, Ludtke A, Wenzel K, Koehnlein M, Schuelke M, Lüdemann L, Schmidt HH. Spuler S, et al. Neurology. 2007 Feb 27;68(9):677-83. doi: 10.1212/01.wnl.0000255939.73424.f8. Neurology. 2007. PMID: 17325275
Dysferlin-deficient muscular dystrophy features amyloidosis.
Spuler S, Carl M, Zabojszcza J, Straub V, Bushby K, Moore SA, Bähring S, Wenzel K, Vinkemeier U, Rocken C. Spuler S, et al. Ann Neurol. 2008 Mar;63(3):323-8. doi: 10.1002/ana.21309. Ann Neurol. 2008. PMID: 18306167
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Osterziel KJ, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C. Geier C, et al. Among authors: spuler s. Hum Mol Genet. 2008 Sep 15;17(18):2753-65. doi: 10.1093/hmg/ddn160. Epub 2008 May 27. Hum Mol Genet. 2008. PMID: 18505755
133 results