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Human Molecular Genetics
|
February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
B 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 dystrophy
U 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 inactivation
S 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, hyperekplexia
R Shiang, S G Ryan, Y Z Zhu, et al.
Journal of Neuroimmunology
|
June 1, 1984
Circulating lymphocyte subpopulations in experimental allergic neuritis
T 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 syndrome
C 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 diseases
N 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 polyneuropathy
T E Feasby, J J Gilbert, W F Brown, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
Human Molecular Genetics
|
February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
B 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 dystrophy
U 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 inactivation
S 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, hyperekplexia
R Shiang, S G Ryan, Y Z Zhu, et al.
Journal of Neuroimmunology
|
June 1, 1984
Circulating lymphocyte subpopulations in experimental allergic neuritis
T 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 syndrome
C 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 diseases
N 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 polyneuropathy
T E Feasby, J J Gilbert, W F Brown, et al.
Page
of 8