Search research articles
Contact Us
Filters
Showing results (11-20 of 25) with videos related to
Page
of 3
Sort By:
Journal of Internal Medicine
|
November 13, 2013
Pathogenic immune mechanisms at the neuromuscular synapse: the role of specific antibody-binding epitopes in myasthenia gravis
M G Huijbers, A F Lipka, J J Plomp, et al.
Neuroscience
|
September 20, 2008
Neuromuscular synaptic function in mice lacking major subsets of gangliosides
F M P Zitman, B Todorov, B C Jacobs, et al.
Annals of Neurology
|
October 20, 1998
Acquired slow-channel syndrome: a form of myasthenia gravis with prolonged open time of the acetylcholine receptor channel
A R Wintzen, J J Plomp, P C Molenaar, et al.
European Journal of Neurology
|
June 3, 2015
The expanding field of IgG4-mediated neurological autoimmune disorders
M G Huijbers, L A Querol, E H Niks, et al.
Neuroscience
|
December 13, 2006
Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice
S Kaja, R C G van de Ven, L A M Broos, et al.
Neuroscience
|
January 13, 2006
alpha-Neurexins are required for efficient transmitter release and synaptic homeostasis at the mouse neuromuscular junction
M S Sons, N Busche, N Strenzke, et al.
Annals of Neurology
|
November 1, 1995
Acquired neuromyotonia: evidence for autoantibodies directed against K+ channels of peripheral nerves
P Shillito, P C Molenaar, A Vincent, et al.
The Journal of Clinical Investigation
|
September 24, 1999
Monoclonal antibodies raised against Guillain-Barré syndrome-associated Campylobacter jejuni lipopolysaccharides react with neuronal gangliosides and paralyze muscle-nerve preparations
C S Goodyear, G M O'Hanlon, J J Plomp, et al.
Plos One
|
May 16, 2018
Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy
S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, et al.
Plos One
|
August 11, 2017
Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F
S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Journal of Internal Medicine
|
November 13, 2013
Pathogenic immune mechanisms at the neuromuscular synapse: the role of specific antibody-binding epitopes in myasthenia gravis
M G Huijbers, A F Lipka, J J Plomp, et al.
Neuroscience
|
September 20, 2008
Neuromuscular synaptic function in mice lacking major subsets of gangliosides
F M P Zitman, B Todorov, B C Jacobs, et al.
Annals of Neurology
|
October 20, 1998
Acquired slow-channel syndrome: a form of myasthenia gravis with prolonged open time of the acetylcholine receptor channel
A R Wintzen, J J Plomp, P C Molenaar, et al.
European Journal of Neurology
|
June 3, 2015
The expanding field of IgG4-mediated neurological autoimmune disorders
M G Huijbers, L A Querol, E H Niks, et al.
Neuroscience
|
December 13, 2006
Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice
S Kaja, R C G van de Ven, L A M Broos, et al.
Neuroscience
|
January 13, 2006
alpha-Neurexins are required for efficient transmitter release and synaptic homeostasis at the mouse neuromuscular junction
M S Sons, N Busche, N Strenzke, et al.
Annals of Neurology
|
November 1, 1995
Acquired neuromyotonia: evidence for autoantibodies directed against K+ channels of peripheral nerves
P Shillito, P C Molenaar, A Vincent, et al.
The Journal of Clinical Investigation
|
September 24, 1999
Monoclonal antibodies raised against Guillain-Barré syndrome-associated Campylobacter jejuni lipopolysaccharides react with neuronal gangliosides and paralyze muscle-nerve preparations
C S Goodyear, G M O'Hanlon, J J Plomp, et al.
Plos One
|
May 16, 2018
Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy
S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, et al.
Plos One
|
August 11, 2017
Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F
S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, et al.
Page
of 3