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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: schmidt hh, schmidt 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.
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. Among authors: schmidt hh. Neurology. 2007 Feb 27;68(9):677-83. doi: 10.1212/01.wnl.0000255939.73424.f8. Neurology. 2007. PMID: 17325275
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.
[Interdisciplinary guidelines on diagnosis and treatment for extracerebral amyloidoses--published by the German Society of Amyloid Diseases (www.amyloid.de)].
Röcken C, Ernst J, Hund E, Michels H, Perz J, Saeger W, Sezer O, Spuler S, Willig F, Schmidt HH; Deutsche Gesellschaft für Amyloid-Krankheiten e.V. Röcken C, et al. Among authors: schmidt hh. Dtsch Med Wochenschr. 2006 Jul 7;131(27 Suppl 2):S45-66. doi: 10.1055/s-2006-947836. Dtsch Med Wochenschr. 2006. PMID: 16835821 German.
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy.
Perrot A, Hussein S, Ruppert V, Schmidt HH, Wehnert MS, Duong NT, Posch MG, Panek A, Dietz R, Kindermann I, Böhm M, Michalewska-Wludarczyk A, Richter A, Maisch B, Pankuweit S, Ozcelik C. Perrot A, et al. Among authors: schmidt hh. Basic Res Cardiol. 2009 Jan;104(1):90-9. doi: 10.1007/s00395-008-0748-6. Epub 2008 Sep 15. Basic Res Cardiol. 2009. PMID: 18795223
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
Perrot A, Sigusch HH, Nägele H, Genschel J, Lehmkuhl H, Hetzer R, Geier C, Leon Perez V, Reinhard D, Dietz R, Josef Osterziel K, Schmidt HH. Perrot A, et al. Among authors: schmidt hh. Eur J Heart Fail. 2006 Aug;8(5):484-93. doi: 10.1016/j.ejheart.2005.11.004. Epub 2006 Jan 4. Eur J Heart Fail. 2006. PMID: 16386954 Free article.
LMNA mutations in cardiac transplant recipients.
Pethig K, Genschel J, Peters T, Wilhelmi M, Flemming P, Lochs H, Haverich A, Schmidt HH. Pethig K, et al. Among authors: schmidt hh. Cardiology. 2005;103(2):57-62. doi: 10.1159/000082048. Epub 2004 Nov 10. Cardiology. 2005. PMID: 15539782
523 results