Search research articles
Contact Us
Filters
Showing results (91-100 of 145) with videos related to
Page
of 15
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 1, 1992
Chronic demyelinating polyneuropathy associated with eosinophilia-myalgia syndrome
M 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 9q34
P 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 ganglioside
A Pestronk, D R Cornblath, A A Ilyas, et al.
Neurology
|
March 1, 1997
Patterns of recovery in the Guillain-Barre syndromes
T W Ho, C Y Li, D R Cornblath, et al.
Neurology
|
October 1, 1995
Cutaneous innervation in sensory neuropathies: evaluation by skin biopsy
B 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 syndrome
C 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 neuropathy
H 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 9q34
I P Blair, C L Bennett, A Abel, et al.
Annals of Neurology
|
March 1, 1993
Multifocal motor neuropathy: response to human immune globulin
V Chaudhry, A M Corse, D R Cornblath, et al.
Muscle & Nerve
|
September 1, 1991
Conduction block in diabetic neuropathy
S R Abu-Shakra, D R Cornblath, O L Avila, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 145) with videos related to
Sort By:
Page
of 15
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 1, 1992
Chronic demyelinating polyneuropathy associated with eosinophilia-myalgia syndrome
M 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 9q34
P 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 ganglioside
A Pestronk, D R Cornblath, A A Ilyas, et al.
Neurology
|
March 1, 1997
Patterns of recovery in the Guillain-Barre syndromes
T W Ho, C Y Li, D R Cornblath, et al.
Neurology
|
October 1, 1995
Cutaneous innervation in sensory neuropathies: evaluation by skin biopsy
B 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 syndrome
C 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 neuropathy
H 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 9q34
I P Blair, C L Bennett, A Abel, et al.
Annals of Neurology
|
March 1, 1993
Multifocal motor neuropathy: response to human immune globulin
V Chaudhry, A M Corse, D R Cornblath, et al.
Muscle & Nerve
|
September 1, 1991
Conduction block in diabetic neuropathy
S R Abu-Shakra, D R Cornblath, O L Avila, et al.
Page
of 15