Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: weakness,generalized (Click to remove) Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 A 30-year-old Man with Progressive Weakness and Atrophy Neurol 87:e227-e230, Quinn, C.,et al, 2016 Diagnosis and Etiology of Congenital Muscular Dystrophy Neurol 71:312-321,308, Peat,R.A.,et al., 2008 Muscle Pain after Exercise Lancet 353:1062, Nielen,C.&Mazzone,P., 1999 Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining Neurol 46:810-814, Connolly,A.M.,et al, 1996 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature Arch Neurol 50:481-488, Hardiman,O.,et al, 1993 Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 Case Records of MGH-NEJM 289:366 1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973 Central Nervous System Manifestations of Periarteritis Nodosa Neurol 15:114, Ford,R.G.,et al, 1965 Showing articles 0 to 10 of 10