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A F Hahn

Showing results (61-70 of 78) with videos related to

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Neurology|April 23, 2003
Interferon beta-1a as an investigational treatment for CIDPJ-M Vallat, A F Hahn, J-M Léger, et al.
Brain : a Journal of Neurology|August 1, 1987
Critical illness polyneuropathy. A complication of sepsis and multiple organ failureD W Zochodne, C F Bolton, G A Wells, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth diseaseA F Hahn, C F Bolton, C M White, et al.
Muscle & Nerve|May 22, 2001
Severe infantile axonal neuropathy with respiratory failureJ M Wilmshurst, A Bye, C Rittey, et al.
Brain : a Journal of Neurology|December 1, 1986
An acute axonal form of Guillain-Barré polyneuropathyT E Feasby, J J Gilbert, W F Brown, et al.
Neurology|April 13, 2005
Reliability and validity of the CMT neuropathy score as a measure of disabilityM E Shy, J Blake, K Krajewski, et al.
Neurology|December 22, 1999
A novel sodium channel mutation in a family with hypokalemic periodic paralysisD E Bulman, K A Scoggan, M D van Oene, et al.
Brain : a Journal of Neurology|August 1, 1996
Plasma-exchange therapy in chronic inflammatory demyelinating polyneuropathy. A double-blind, sham-controlled, cross-over studyA F Hahn, C F Bolton, N Pillay, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomyF P Thomas, T J Geller, A F Hahn, et al.
Genomics|July 1, 1990
Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17P J McAlpine, T E Feasby, A F Hahn, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Neurology|April 23, 2003
Interferon beta-1a as an investigational treatment for CIDPJ-M Vallat, A F Hahn, J-M Léger, et al.
Brain : a Journal of Neurology|August 1, 1987
Critical illness polyneuropathy. A complication of sepsis and multiple organ failureD W Zochodne, C F Bolton, G A Wells, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth diseaseA F Hahn, C F Bolton, C M White, et al.
Muscle & Nerve|May 22, 2001
Severe infantile axonal neuropathy with respiratory failureJ M Wilmshurst, A Bye, C Rittey, et al.
Brain : a Journal of Neurology|December 1, 1986
An acute axonal form of Guillain-Barré polyneuropathyT E Feasby, J J Gilbert, W F Brown, et al.
Neurology|April 13, 2005
Reliability and validity of the CMT neuropathy score as a measure of disabilityM E Shy, J Blake, K Krajewski, et al.
Neurology|December 22, 1999
A novel sodium channel mutation in a family with hypokalemic periodic paralysisD E Bulman, K A Scoggan, M D van Oene, et al.
Brain : a Journal of Neurology|August 1, 1996
Plasma-exchange therapy in chronic inflammatory demyelinating polyneuropathy. A double-blind, sham-controlled, cross-over studyA F Hahn, C F Bolton, N Pillay, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomyF P Thomas, T J Geller, A F Hahn, et al.
Genomics|July 1, 1990
Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17P J McAlpine, T E Feasby, A F Hahn, et al.
Pageof 8