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Journal of the Neurological Sciences|September 21, 2007
The morbidity and outcome of patients with Guillain-Barré syndrome admitted to the intensive care unitRajat Dhar, Larry Stitt, Angelika F HahnMuscle & Nerve|November 3, 2009
Clinical and electrophysiological parameters distinguishing acute-onset chronic inflammatory demyelinating polyneuropathy from acute inflammatory demyelinating polyneuropathyAnnie Dionne, Michael W Nicolle, Angelika F HahnJournal of Neurology, Neurosurgery, and Psychiatry|December 18, 2014
Intravenous immunoglobulin response in treatment-naïve chronic inflammatory demyelinating polyradiculoneuropathyKrista Kuitwaard, Angelika F Hahn, Marinus Vermeulen, et al.Journal of the Neurological Sciences|March 5, 2003
Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathyThierry Kuntzer, Murielle Dunand, Daniel F Schorderet, et al.Pathology, Research and Practice|February 6, 2016
Amyloid deposition in extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue: A clinicopathologic study of 5 casesQi Zhang, Cady Pocrnich, Annie Kurian, et al.Annals of Neurology|April 1, 2009
Placebo-controlled trial of rituximab in IgM anti-myelin-associated glycoprotein antibody demyelinating neuropathyMarinos C Dalakas, Goran Rakocevic, Mohammad Salajegheh, et al.Annals of Clinical and Translational Neurology|November 16, 2016
Novel NALCN variant: altered respiratory and circadian rhythm, anesthetic sensitivityBernarda Lozic, Stefan Johansson, Sanja Lovric Kojundzic, et al.Annals of the New York Academy of Sciences|November 1, 2017
Genotype/Phenotype Correlations in X-Linked Dominant Charcot-Marie-Tooth DiseaseAngelika F Hahn, Charles F Bolton, Christopher M White, et al.Journal of the Peripheral Nervous System : JPNS|April 15, 2014
A controlled trial of intravenous immunoglobulin in multifocal motor neuropathyAngelika F Hahn, Said R Beydoun, Victoria Lawson, et al.Annals of Clinical and Translational Neurology|December 26, 2014
Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomyMariarosa A B Melone, Michael J Pellegrino, Maria Nolano, et al.Pageof 3