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A F Hahn

Showing results (51-60 of 78) with videos related to

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Human Molecular Genetics|February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.
Brain : a Journal of Neurology|December 1, 1996
Central and peripheral respiratory electrophysiological studies in myotonic dystrophyU A Zifko, A F Hahn, H Remtulla, et al.
The Journal of Clinical Investigation|August 10, 2000
A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivationS Bendahhou, T R Cummins, A F Hahn, et al.
Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.
Journal of Neuroimmunology|June 1, 1984
Circulating lymphocyte subpopulations in experimental allergic neuritisT E Feasby, R Mazaheri, A F Hahn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1986
Critically ill polyneuropathy: electrophysiological studies and differentiation from Guillain-Barré syndromeC F Bolton, D A Laverty, J D Brown, et al.
Journal of the Neurological Sciences|June 1, 1993
Severe axonal degeneration in acute Guillain-Barré syndrome: evidence of two different mechanisms?T E Feasby, A F Hahn, W F Brown, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2001
Use of intravenous gamma globulins in neuroimmunologic diseasesN Latov, V Chaudhry, C L Koski, et al.
Acta Neuropathologica|January 1, 1994
Nerve biopsy findings in Niemann-Pick type II (NPC)A F Hahn, J J Gilbert, C Kwarciak, et al.
Neurology|February 1, 1987
Acute "axonal" Guillain-Barré polyneuropathyT E Feasby, J J Gilbert, W F Brown, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.
Brain : a Journal of Neurology|December 1, 1996
Central and peripheral respiratory electrophysiological studies in myotonic dystrophyU A Zifko, A F Hahn, H Remtulla, et al.
The Journal of Clinical Investigation|August 10, 2000
A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivationS Bendahhou, T R Cummins, A F Hahn, et al.
Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.
Journal of Neuroimmunology|June 1, 1984
Circulating lymphocyte subpopulations in experimental allergic neuritisT E Feasby, R Mazaheri, A F Hahn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1986
Critically ill polyneuropathy: electrophysiological studies and differentiation from Guillain-Barré syndromeC F Bolton, D A Laverty, J D Brown, et al.
Journal of the Neurological Sciences|June 1, 1993
Severe axonal degeneration in acute Guillain-Barré syndrome: evidence of two different mechanisms?T E Feasby, A F Hahn, W F Brown, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2001
Use of intravenous gamma globulins in neuroimmunologic diseasesN Latov, V Chaudhry, C L Koski, et al.
Acta Neuropathologica|January 1, 1994
Nerve biopsy findings in Niemann-Pick type II (NPC)A F Hahn, J J Gilbert, C Kwarciak, et al.
Neurology|February 1, 1987
Acute "axonal" Guillain-Barré polyneuropathyT E Feasby, J J Gilbert, W F Brown, et al.
Pageof 8