Spuler S - Search Results

1

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.

2

[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.

3

Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy.

Wenzel K, Zabojszcza J, Carl M, Taubert S, Lass A, Harris CL, Ho M, Schulz H, Hummel O, Hubner N, Osterziel KJ, Spuler S. Wenzel K, et al. Among authors: spuler s. J Immunol. 2005 Nov 1;175(9):6219-25. doi: 10.4049/jimmunol.175.9.6219. J Immunol. 2005. PMID: 16237120

4

Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.

Wenzel K, Carl M, Perrot A, Zabojszcza J, Assadi M, Ebeling M, Geier C, Robinson PN, Kress W, Osterziel KJ, Spuler S. Wenzel K, et al. Among authors: spuler s. Hum Mutat. 2006 Jun;27(6):599-600. doi: 10.1002/humu.9424. Hum Mutat. 2006. PMID: 16705711

5

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

6

Peroxisome proliferator-activated receptor-gamma C190S mutation causes partial lipodystrophy.

Lüdtke A, Buettner J, Wu W, Muchir A, Schroeter A, Zinn-Justin S, Spuler S, Schmidt HH, Worman HJ. Lüdtke A, et al. Among authors: spuler s. J Clin Endocrinol Metab. 2007 Jun;92(6):2248-55. doi: 10.1210/jc.2005-2624. Epub 2007 Mar 13. J Clin Endocrinol Metab. 2007. PMID: 17356052

7

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

8

LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance.

Boschmann M, Engeli S, Moro C, Luedtke A, Adams F, Gorzelniak K, Rahn G, Mähler A, Dobberstein K, Krüger A, Schmidt S, Spuler S, Luft FC, Smith SR, Schmidt HH, Jordan J. Boschmann M, et al. Among authors: spuler s. J Clin Endocrinol Metab. 2010 Apr;95(4):1634-43. doi: 10.1210/jc.2009-1293. Epub 2010 Feb 3. J Clin Endocrinol Metab. 2010. PMID: 20130076 Free PMC article.

9

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.

Knoblauch H, Geier C, Adams S, Budde B, Rudolph A, Zacharias U, Schulz-Menger J, Spuler A, Yaou RB, Nürnberg P, Voit T, Bonne G, Spuler S. Knoblauch H, et al. Among authors: spuler a, spuler s. Ann Neurol. 2010 Jan;67(1):136-40. doi: 10.1002/ana.21839. Ann Neurol. 2010. PMID: 20186852

10

Long-term treatment experience in a subject with Dunnigan-type familial partial lipodystrophy: efficacy of rosiglitazone.

Lüdtke A, Heck K, Genschel J, Mehnert H, Spuler S, Worman HJ, Schmidt HH. Lüdtke A, et al. Among authors: spuler s. Diabet Med. 2005 Nov;22(11):1611-3. doi: 10.1111/j.1464-5491.2005.01757.x. Diabet Med. 2005. PMID: 16241930

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