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Showing articles 0 to 12 of 12 Filter Applied: weakness,generalized (Click to remove) Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 A Teenager with Shortness of Breath and Difficulty Walking Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021 Subacute Paresis in a 28-year-old man with HIV Neurol 90:432-435, Harada, Y.,et al, 2018 A 42-year-old man with unilateral leg weakness Neurol 90:e1085-e1090, Schneider, R.,et al, 2018 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 Diagnosis and Etiology of Congenital Muscular Dystrophy Neurol 71:312-321,308, Peat,R.A.,et al., 2008 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 Osteomalacic Myopathy Muscle & Nerve 17:578-580994., Russell,J.A., 1994 Clinicopath Conf Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994 The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988 Carnitine Deficiency Acute Postpartum Crisis Ann Neurol 4:558-561, Angelini,C.,et al, 1978 Showing articles 0 to 12 of 12