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Neurol 79:195-196, Tofaris,G.K.,et al, 2012
Myelitis-Predominant Agressive Phenotype:Unveiling Unique Paterns of Late-Onset Neuromyelitis Optica Spectrum Disorders
Ann Neurol 99:1139-1151, Pu,Y-L.,et al, 2026
Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025
Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020
Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016
Late-Onset Anti-NMDA Receptor Encephalitis
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Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011
Mysterious Falls and a Nasal Voice
Lancet 370:712, Bhandari,A. &Adenwalla,F., 2007
Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000
Late-Onset Myasthenia Graivs,A Changing Scene
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Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996
Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994
Treatable Gait Disorder & Polyneuropathy Assoc with High Titer Serum IgM Binding to Atg that Copurify with MAG
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