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A F Hahn

Showing results (71-80 of 78) with videos related to

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Muscle & Nerve|January 20, 2000
Impact of plasma exchange on indices of demyelination in chronic inflammatory demyelinating polyradiculoneuropathyN L Ashworth, D W Zochodne, A F Hahn, et al.
Journal of the Neurological Sciences|April 20, 2010
Cold-induced sweating syndrome: CISS1 and CISS2: manifestations from infancy to adulthood. Four new casesA F Hahn, P E Waaler, P H Kvistad, et al.
Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM E Shy, C Siskind, E R Swan, et al.
Neurology|September 25, 2003
Practice parameter: immunotherapy for Guillain-Barré syndrome: report of the Quality Standards Subcommittee of the American Academy of NeurologyR A C Hughes, E F M Wijdicks, R Barohn, et al.
American Journal of Human Genetics|July 31, 1998
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qterM Hirano, J Garcia-de-Yebenes, A C Jones, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Annals of Neurology|December 1, 1991
Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel geneG C Ebers, A L George, R L Barchi, et al.
Journal of the Neurological Sciences|December 19, 2008
Derivation and validation of diagnostic criteria for chronic inflammatory demyelinating polyneuropathyC L Koski, M Baumgarten, L S Magder, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Muscle & Nerve|January 20, 2000
Impact of plasma exchange on indices of demyelination in chronic inflammatory demyelinating polyradiculoneuropathyN L Ashworth, D W Zochodne, A F Hahn, et al.
Journal of the Neurological Sciences|April 20, 2010
Cold-induced sweating syndrome: CISS1 and CISS2: manifestations from infancy to adulthood. Four new casesA F Hahn, P E Waaler, P H Kvistad, et al.
Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM E Shy, C Siskind, E R Swan, et al.
Neurology|September 25, 2003
Practice parameter: immunotherapy for Guillain-Barré syndrome: report of the Quality Standards Subcommittee of the American Academy of NeurologyR A C Hughes, E F M Wijdicks, R Barohn, et al.
American Journal of Human Genetics|July 31, 1998
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qterM Hirano, J Garcia-de-Yebenes, A C Jones, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Annals of Neurology|December 1, 1991
Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel geneG C Ebers, A L George, R L Barchi, et al.
Journal of the Neurological Sciences|December 19, 2008
Derivation and validation of diagnostic criteria for chronic inflammatory demyelinating polyneuropathyC L Koski, M Baumgarten, L S Magder, et al.
Pageof 8