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Muscle & Nerve
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April 5, 2002
Detection and prevalence of alpha-latrotoxin-like effects of serum from patients with Guillain-Barré syndrome
Bart C Jacobs, Roland W M Bullens, Graham M O'Hanlon, et al.
Current Opinion in Neurology
|
June 5, 2002
Calcium channel mutations and migraine
Esther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 2, 2019
Natural disease history of the D2<i>-mdx</i> mouse model for Duchenne muscular dystrophy
Maaike van Putten, Kayleigh Putker, Maurice Overzier, et al.
Glia
|
June 22, 2005
Anti-disialosyl antibodies mediate selective neuronal or Schwann cell injury at mouse neuromuscular junctions
Susan K Halstead, Ian Morrison, Graham M O'Hanlon, et al.
The Journal of Clinical Investigation
|
February 7, 2012
Anti-ganglioside antibody internalization attenuates motor nerve terminal injury in a mouse model of acute motor axonal neuropathy
Simon N Fewou, Angie Rupp, Lauren E Nickolay, et al.
Muscle & Nerve
|
March 29, 2005
Concanavalin A inhibits pathophysiological effects of anti-ganglioside GQ1b antibodies at the mouse neuromuscular synapse
Roland W M Bullens, Susan K Halstead, Graham M O'Hanlon, et al.
Journal of Neuroimmunology
|
July 31, 2008
The role of complement and complement regulators in mediating motor nerve terminal injury in murine models of Guillain-Barré syndrome
Hugh J Willison, Susan K Halstead, Erin Beveridge, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 10, 2006
Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction
Mariska C van der Plas, Gonneke S K Pilgram, Jaap J Plomp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 15, 2002
Complex gangliosides at the neuromuscular junction are membrane receptors for autoantibodies and botulinum neurotoxin but redundant for normal synaptic function
Roland W M Bullens, Graham M O'Hanlon, Eric Wagner, et al.
Neurobiology of Aging
|
February 24, 2009
Neuromuscular synaptic transmission in aged ganglioside-deficient mice
Femke M P Zitman, Boyan Todorov, Jan J Verschuuren, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 68) with videos related to
Sort By:
Page
of 7
Muscle & Nerve
|
April 5, 2002
Detection and prevalence of alpha-latrotoxin-like effects of serum from patients with Guillain-Barré syndrome
Bart C Jacobs, Roland W M Bullens, Graham M O'Hanlon, et al.
Current Opinion in Neurology
|
June 5, 2002
Calcium channel mutations and migraine
Esther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 2, 2019
Natural disease history of the D2<i>-mdx</i> mouse model for Duchenne muscular dystrophy
Maaike van Putten, Kayleigh Putker, Maurice Overzier, et al.
Glia
|
June 22, 2005
Anti-disialosyl antibodies mediate selective neuronal or Schwann cell injury at mouse neuromuscular junctions
Susan K Halstead, Ian Morrison, Graham M O'Hanlon, et al.
The Journal of Clinical Investigation
|
February 7, 2012
Anti-ganglioside antibody internalization attenuates motor nerve terminal injury in a mouse model of acute motor axonal neuropathy
Simon N Fewou, Angie Rupp, Lauren E Nickolay, et al.
Muscle & Nerve
|
March 29, 2005
Concanavalin A inhibits pathophysiological effects of anti-ganglioside GQ1b antibodies at the mouse neuromuscular synapse
Roland W M Bullens, Susan K Halstead, Graham M O'Hanlon, et al.
Journal of Neuroimmunology
|
July 31, 2008
The role of complement and complement regulators in mediating motor nerve terminal injury in murine models of Guillain-Barré syndrome
Hugh J Willison, Susan K Halstead, Erin Beveridge, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 10, 2006
Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction
Mariska C van der Plas, Gonneke S K Pilgram, Jaap J Plomp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 15, 2002
Complex gangliosides at the neuromuscular junction are membrane receptors for autoantibodies and botulinum neurotoxin but redundant for normal synaptic function
Roland W M Bullens, Graham M O'Hanlon, Eric Wagner, et al.
Neurobiology of Aging
|
February 24, 2009
Neuromuscular synaptic transmission in aged ganglioside-deficient mice
Femke M P Zitman, Boyan Todorov, Jan J Verschuuren, et al.
Page
of 7