Differential (Click to cross reference) anxiety calf hypertrophy calpain III deficiency cardiomyopathy children chromosomal abnormality chromosome 17 chromosome 7 congestive heart failure creatine phosphokinase(CPK)elevated dystonia dystrophin dystrophin associated proteins electron microscopy epsilon sarcoglycan gene familial gene gene mutation genetic neurologic disorders misdiagnosis molecular genetics movement disorder muscle biopsy muscle weakness, proximal muscular dystrophy muscular dystrophy, cardiovascular changes with muscular dystrophy, classification muscular dystrophy, congenital muscular dystrophy, congenital, Fukuyama type muscular dystrophy, Duchenne muscular dystrophy, dystrophin normal muscular dystrophy, female occurrence of muscular dystrophy, limb-girdle myoclonic dystonia myoclonus myoclonus, action myopathy prognosis psychiatric problems in neurologic disorders review article sarcoglycan sarcoglycanopathy spastic dysphonia speech disorder treatment of neurologic disorder weakness, progressive wheelchair

Showing articles 0 to 10 of 10 Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012 The Clinical Spectrum of Sarcoglycanopathies Neurol 52:176-179, Angelini,C.,et al, 1999 Mutations in the Sarcoglycan Genes in Patients with Myopathy NEJM 336:618-624, Duggan,D.J.,et al, 1997 The Muscular Dystrophies-Clarity or Chaos NEJM 336 650-651, Dubowitz,V., 1997 Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy Neurol 48:1227-1234, Eymard,B.,et al, 1997 Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy NEJM 334:362-366, Fadic,R.,et al, 1996 Clinical Heterogeneity of Adhalin Deficiency Ann Neurol 39:196-202, Morandi,L.,et al, 1996 Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995 Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy Lancet 341:521-522, Matsumura,K.,et al, 1993 Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma Neurol 43:795-800, Ohlendieck,K.,et al, 1993 Showing articles 0 to 10 of 10