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Showing articles 0 to 13 of 13 Filter Applied: weakness,generalized (Click to remove) Man with Recurrent Paralysis and Cerebral White Matter Lesions JAMA Neurol 74:599-600, Xiao, F., 2017 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 A 42-year-old man with unilateral leg weakness Neurol 90:e1085-e1090, Schneider, R.,et al, 2018 Spinal Muscular Atrophy Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008 Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 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 Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008 Reversible ALS-Like Disorder in HIV Infection Neurol 57:995-1001,945, Moulignier,A.,et al, 2001 A Woman Who Left Her Wheelchair Lancet 353:806, Mingrone,G.,et al, 1999 Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia NEJM 340:1661-1669, , 1999 Clinicopath Conf Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997 Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 Showing articles 0 to 13 of 13