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D R Cornblath

Showing results (91-100 of 145) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1992
Chronic demyelinating polyneuropathy associated with eosinophilia-myalgia syndromeM L Freimer, J D Glass, V Chaudhry, et al.
American Journal of Human Genetics|April 29, 1998
Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34P F Chance, B A Rabin, S G Ryan, et al.
Annals of Neurology|July 1, 1988
A treatable multifocal motor neuropathy with antibodies to GM1 gangliosideA Pestronk, D R Cornblath, A A Ilyas, et al.
Neurology|March 1, 1997
Patterns of recovery in the Guillain-Barre syndromesT W Ho, C Y Li, D R Cornblath, et al.
Neurology|October 1, 1995
Cutaneous innervation in sensory neuropathies: evaluation by skin biopsyB G McCarthy, S T Hsieh, A Stocks, et al.
Annals of Neurology|June 1, 1996
A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndromeC M Gomez, R Maselli, J Gammack, et al.
Journal of Neuroimmunology|December 1, 1989
Anti-GM1 ganglioside antibodies with differing fine specificities in patients with multifocal motor neuropathyH Baba, G C Daune, A A Ilyas, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Annals of Neurology|March 1, 1993
Multifocal motor neuropathy: response to human immune globulinV Chaudhry, A M Corse, D R Cornblath, et al.
Muscle & Nerve|September 1, 1991
Conduction block in diabetic neuropathyS R Abu-Shakra, D R Cornblath, O L Avila, et al.
Pageof 15

Showing results (91-100 of 145) with videos related to

Sort By:
Pageof 15
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1992
Chronic demyelinating polyneuropathy associated with eosinophilia-myalgia syndromeM L Freimer, J D Glass, V Chaudhry, et al.
American Journal of Human Genetics|April 29, 1998
Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34P F Chance, B A Rabin, S G Ryan, et al.
Annals of Neurology|July 1, 1988
A treatable multifocal motor neuropathy with antibodies to GM1 gangliosideA Pestronk, D R Cornblath, A A Ilyas, et al.
Neurology|March 1, 1997
Patterns of recovery in the Guillain-Barre syndromesT W Ho, C Y Li, D R Cornblath, et al.
Neurology|October 1, 1995
Cutaneous innervation in sensory neuropathies: evaluation by skin biopsyB G McCarthy, S T Hsieh, A Stocks, et al.
Annals of Neurology|June 1, 1996
A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndromeC M Gomez, R Maselli, J Gammack, et al.
Journal of Neuroimmunology|December 1, 1989
Anti-GM1 ganglioside antibodies with differing fine specificities in patients with multifocal motor neuropathyH Baba, G C Daune, A A Ilyas, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Annals of Neurology|March 1, 1993
Multifocal motor neuropathy: response to human immune globulinV Chaudhry, A M Corse, D R Cornblath, et al.
Muscle & Nerve|September 1, 1991
Conduction block in diabetic neuropathyS R Abu-Shakra, D R Cornblath, O L Avila, et al.
Pageof 15