Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
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A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
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Congenital Muscular Dystrophy
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
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Cockayne Syndrome: Review of 140 Cases
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Fucosidosis Revisited:A Review of 77 Patients
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Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
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Congenital Muscular Dystrophy
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Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
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Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988
Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988
Central Core Disease, Clinical Features in 13 Patients
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Clinical Epidemology of Toxic-Oil Syndrome
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Congenital Myotonic Dystrophy
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Emery-Dreifuss Muscular Dystrophy
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
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