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A Pestronk

Showing results (121-130 of 151) with videos related to

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The New England Journal of Medicine|January 20, 1977
Myasthenia gravis. Study of humoral immune mechanisms by passive transfer to miceK V Toyka, D B Drachman, D E Griffin, et al.
Archives of Neurology|April 1, 1991
Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy GroupR C Griggs, R T Moxley, J R Mendell, et al.
Neurology|February 12, 2004
Sensory exam with a quantitative tuning fork: rapid, sensitive and predictive of SNAP amplitudeA Pestronk, J Florence, T Levine, 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|August 11, 2010
Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32M B Harms, P Allred, R Gardner, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2015
Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvementN A Goyal, T M Cash, U Alam, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 18, 2008
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementiaC C Weihl, P Temiz, S E Miller, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Distribution of ten laminin chains in dystrophic and regenerating musclesB L Patton, A M Connoll, P T Martin, et al.
Neurology|March 1, 1991
Polyneuropathy syndromes associated with serum antibodies to sulfatide and myelin-associated glycoproteinA Pestronk, F Li, J Griffin, et al.
Pageof 16

Showing results (121-130 of 151) with videos related to

Sort By:
Pageof 16
The New England Journal of Medicine|January 20, 1977
Myasthenia gravis. Study of humoral immune mechanisms by passive transfer to miceK V Toyka, D B Drachman, D E Griffin, et al.
Archives of Neurology|April 1, 1991
Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy GroupR C Griggs, R T Moxley, J R Mendell, et al.
Neurology|February 12, 2004
Sensory exam with a quantitative tuning fork: rapid, sensitive and predictive of SNAP amplitudeA Pestronk, J Florence, T Levine, 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|August 11, 2010
Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32M B Harms, P Allred, R Gardner, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2015
Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvementN A Goyal, T M Cash, U Alam, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 18, 2008
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementiaC C Weihl, P Temiz, S E Miller, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Distribution of ten laminin chains in dystrophic and regenerating musclesB L Patton, A M Connoll, P T Martin, et al.
Neurology|March 1, 1991
Polyneuropathy syndromes associated with serum antibodies to sulfatide and myelin-associated glycoproteinA Pestronk, F Li, J Griffin, et al.
Pageof 16