Diagnostic strategy for limb-girdle muscular dystrophies
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference17 articles.
1. A new locus on 3p23-p25 for an autosomal dominant limb-girdle muscular dystrophy, LGMD1H;Bisceglia;Eur J Hum Genet,2010
2. The limb-girdle muscular dystrophies-diagnostic strategies;Bushby;Biochim Biophys Acta,2007
3. Dystrophies musculaires des ceintures : stratégie diagnostique, bases moléculaires;Campana-Salort;Rev Rhum,2008
4. Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern;Deconinck;Neuromuscul Disord,2010
5. Myopathy associated with anti-signal recognition peptide antibodies: clinical heterogeneity contrast with stereotyped histopathology;Dimitri;Muscle Nerve,2007
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1. Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations;Neuromuscular Disorders;2015-07
2. The Muscular Dystrophies;Genetic Counseling for Adult Neurogenetic Disease;2014-10-14
3. Muscle diseases with prominent joint contractures: Main entities and diagnostic strategy;Revue Neurologique;2013-08
4. Maladies musculaires en réanimation. Quand les évoquer ? Comment orienter la recherche diagnostique ?;Réanimation;2012-09
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