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Journal Abstract Search
403 related items for PubMed ID: 18779423
1. Cardiac involvement in patients with limb-girdle muscular dystrophy type 2 and Becker muscular dystrophy. Sveen ML, Thune JJ, Køber L, Vissing J. Arch Neurol; 2008 Sep; 65(9):1196-201. PubMed ID: 18779423 [Abstract] [Full Text] [Related]
3. High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. Sveen ML, Schwartz M, Vissing J. Ann Neurol; 2006 May; 59(5):808-15. PubMed ID: 16634037 [Abstract] [Full Text] [Related]
5. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation. Pathak P, Sharma MC, Sarkar C, Jha P, Suri V, Mohd H, Singh S, Bhatia R, Gulati S. Neurol India; 2010 May; 58(4):549-54. PubMed ID: 20739790 [Abstract] [Full Text] [Related]
6. Cardiac involvement over 10 years in myotonic and Becker muscular dystrophy and mitochondrial disorder. Finsterer J, Stöllberger C, Blazek G, Kunafer M, Prager E. Int J Cardiol; 2007 Jul 10; 119(2):176-84. PubMed ID: 17258336 [Abstract] [Full Text] [Related]
9. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies. ten Dam L, van der Kooi AJ, van Wattingen M, de Haan RJ, de Visser M. Neurology; 2012 Oct 16; 79(16):1716-23. PubMed ID: 23035061 [Abstract] [Full Text] [Related]
10. LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene. Sáenz A, Leturcq F, Cobo AM, Poza JJ, Ferrer X, Otaegui D, Camaño P, Urtasun M, Vílchez J, Gutiérrez-Rivas E, Emparanza J, Merlini L, Paisán C, Goicoechea M, Blázquez L, Eymard B, Lochmuller H, Walter M, Bonnemann C, Figarella-Branger D, Kaplan JC, Urtizberea JA, Martí-Massó JF, López de Munain A. Brain; 2005 Apr 16; 128(Pt 4):732-42. PubMed ID: 15689361 [Abstract] [Full Text] [Related]
11. Hereditary muscular dystrophies and the heart. Hermans MC, Pinto YM, Merkies IS, de Die-Smulders CE, Crijns HJ, Faber CG. Neuromuscul Disord; 2010 Aug 16; 20(8):479-92. PubMed ID: 20627570 [Abstract] [Full Text] [Related]
12. Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. Darin N, Kroksmark AK, Ahlander AC, Moslemi AR, Oldfors A, Tulinius M. Eur J Paediatr Neurol; 2007 Nov 16; 11(6):353-7. PubMed ID: 17446099 [Abstract] [Full Text] [Related]
13. Resistance training in patients with limb-girdle and becker muscular dystrophies. Sveen ML, Andersen SP, Ingelsrud LH, Blichter S, Olsen NE, Jønck S, Krag TO, Vissing J. Muscle Nerve; 2013 Feb 16; 47(2):163-9. PubMed ID: 23169433 [Abstract] [Full Text] [Related]
14. Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients. Hermanová M, Zapletalová E, Sedlácková J, Chrobáková T, Letocha O, Kroupová I, Zámecník J, Vondrácek P, Mazanec R, Maríková T, Vohánka S, Fajkusová L. Muscle Nerve; 2006 Mar 16; 33(3):424-32. PubMed ID: 16372320 [Abstract] [Full Text] [Related]
15. The heart in Becker muscular dystrophy, facioscapulohumeral dystrophy, and Bethlem myopathy. de Visser M, de Voogt WG, la Rivière GV. Muscle Nerve; 1992 May 16; 15(5):591-6. PubMed ID: 1584251 [Abstract] [Full Text] [Related]
16. Electron microscopic findings of cardiomyopathy with limb girdle muscular dystrophy. Funabiki K, Onishi K, Tanabe M, Kuru S, Konagaya M, Sato F, Ito M, Nakano T. Int J Cardiol; 2005 Jan 16; 98(1):161-2. PubMed ID: 15676184 [Abstract] [Full Text] [Related]
17. Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype? Pizzanelli C, Mancuso M, Galli R, Choub A, Fanin M, Nascimbeni AC, Siciliano G, Murri L. Neurol Sci; 2006 Jun 16; 27(2):134-6. PubMed ID: 16816913 [Abstract] [Full Text] [Related]
18. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Schwartz M, Hertz JM, Sveen ML, Vissing J. Neurology; 2005 May 10; 64(9):1635-7. PubMed ID: 15883334 [Abstract] [Full Text] [Related]