DMW - Deutsche Medizinische Wochenschrift, Table of Contents Dtsch Med Wochenschr 2012; 137(09): 447DOI: 10.1055/s-0031-1298886 Korrespondenz | Correspondence Leserbriefe © Georg Thieme Verlag KG Stuttgart · New YorkNon-Compaction-KardiomyopathieNon-compaction-cardiomyopathyAuthors Author Affiliations J. Finsterer 1 Danube University Krems, Krems C. Stöllberger 2 2nd Medical Department, Krankenanstalt Rudolfstiftung, Vienna, Austria Recommend Article Abstract Buy Article(opens in new window) Previous part of this series:Non-Compaction-KardiomyopathieDtsch Med Wochenschr 2011; 136(16): 820-824DOI: 10.1055/s-0031-1275811 Full Text References Literatur 1 Battaglia A, Shaffer LG. 1p36 Deletion Syndrome. 2008 Feb 1 In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993. Available from http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=del1p36 2 Hermann HP. Non-Compaction-Kardiomyopathie. Dtsch Med Wochenschr 2011; 136: 820-824 3 Hung FC, Huang SC, Jong YJ. Neonatal myotubular myopathy with respiratory distress: report of a case. J Formos Med Assoc 1991; 90: 844-847 4 Mandel K, Grunebaum E, Benson L. Noncompaction of the myocardium associated with Roifman syndrome. Cardiol Young 2001; 11: 240-243 5 Nakayama T, Komiya T, Tyou E et al. Cardiac deformity and dysfunction in facioscapulohumeral dystrophy – electrocardiogram, ECG gate cardiac MRI studies. Rinsho Shinkeigaku 1999; 39: 610-614 6 Rosenmann A, Arad I. Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance. J Med Genet 1974; 11: 91-94 7 Shigeto H, Tamura T, Oya Y et al. Facioscapulohumeral muscular dystrophy with sinus dysfunction. Rinsho Shinkeigaku 2002; 42: 881-884 8 Tsai CH, Huang WS, Tsai FJ et al. X-linked recessive myotubular myopathy proven by muscle biopsy. J Formos Med Assoc 1996; 95: 153-156 9 Wohlgemuth M, van der Kooi EL, van Kesteren RG et al. Ventilatory support in facioscapulohumeral muscular dystrophy. Neurology 2004; 63: 176-178 10 Yamada H, Komiyama A, Suzuki Y et al. A case of non-Fukuyama type congenital muscular dystrophy with progression in early adulthood, ocular involvement, and sensorineural deafness. Rinsho Shinkeigaku 1993; 33: 405-410
