Showing results (1321-1330 of 3,399) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|March 17, 2009
Eosinophilic myositis in calpainopathy: could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?Piraye Serdaroglu Oflazer, Hülya Gundesli, Suzan Zorludemir, et al.
Neuromuscular Disorders : NMD|March 3, 2009
ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyWen-Chen Liang, Aya Ohkuma, Yukiko K Hayashi, et al.
Neuromuscular Disorders : NMD|May 12, 2009
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegiaRoberto Negro, Stefano Zoccolella, Rosa Dell'aglio, et al.
Neuromuscular Disorders : NMD|April 22, 2009
Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementiaConrad C Weihl, Alan Pestronk, Virginia E Kimonis
Neuromuscular Disorders : NMD|November 1, 2008
Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophyPetr Dmitriev, Marc Lipinski, Yegor S Vassetzky
Neuromuscular Disorders : NMD|November 1, 2008
Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenanceJacques S Beckmann, Melissa Spencer
Neuromuscular Disorders : NMD|December 17, 2008
Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relativesHenriett Pikó, Viktor Vancsó, Bálint Nagy, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophySamira Makri, Nigel F Clarke, Pascale Richard, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathyAnita Graceffa, Massimo Russo, Gian Luca Vita, et al.
Neuromuscular Disorders : NMD|January 24, 2009
Novel activation domain derived from Che-1 cofactor coupled with the artificial protein Jazz drives utrophin upregulationAgata Desantis, Annalisa Onori, Maria Grazia Di Certo, et al.
Pageof 340