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Annals of Neurology
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July 1, 1989
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics
A Lombes, J R Mendell, H Nakase, et al.
Neurology
|
August 1, 1994
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis
L J Ptáĉek, R Tawil, R C Griggs, et al.
Neurology
|
September 25, 1999
Brachial amyotrophic diplegia: a slowly progressive motor neuron disorder
J S Katz, G I Wolfe, P B Andersson, et al.
Journal of Neuroscience Research
|
August 15, 1996
Evidence against chronic antigen-specific T lymphocyte activation in myasthenia gravis
A J Infante, P D Infante, C E Jackson, et al.
Neurology
|
April 1, 1998
Toward earlier diagnosis of amyotrophic lateral sclerosis: revised criteria. rhCNTF ALS Study Group
M A Ross, R G Miller, L Berchert, et al.
Neurology
|
February 1, 1996
Immune brachial plexus neuropathy: suggestive evidence for an inflammatory-immune pathogenesis
G A Suarez, C Giannini, E P Bosch, et al.
Annals of Neurology
|
March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis
L J Ptacek, L Gouw, H Kwieciński, et al.
Neurology
|
September 12, 2000
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy
M P Collins, J R Mendell, M I Periquet, et al.
Muscle & Nerve
|
May 20, 1999
Multifocal acquired demyelinating sensory and motor neuropathy: the Lewis-Sumner syndrome
D S Saperstein, A A Amato, G I Wolfe, et al.
Archives of Neurology
|
February 1, 1994
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorder
E Tan, D J Lynn, A A Amato, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 113) with videos related to
Sort By:
Page
of 12
Annals of Neurology
|
July 1, 1989
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics
A Lombes, J R Mendell, H Nakase, et al.
Neurology
|
August 1, 1994
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis
L J Ptáĉek, R Tawil, R C Griggs, et al.
Neurology
|
September 25, 1999
Brachial amyotrophic diplegia: a slowly progressive motor neuron disorder
J S Katz, G I Wolfe, P B Andersson, et al.
Journal of Neuroscience Research
|
August 15, 1996
Evidence against chronic antigen-specific T lymphocyte activation in myasthenia gravis
A J Infante, P D Infante, C E Jackson, et al.
Neurology
|
April 1, 1998
Toward earlier diagnosis of amyotrophic lateral sclerosis: revised criteria. rhCNTF ALS Study Group
M A Ross, R G Miller, L Berchert, et al.
Neurology
|
February 1, 1996
Immune brachial plexus neuropathy: suggestive evidence for an inflammatory-immune pathogenesis
G A Suarez, C Giannini, E P Bosch, et al.
Annals of Neurology
|
March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis
L J Ptacek, L Gouw, H Kwieciński, et al.
Neurology
|
September 12, 2000
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy
M P Collins, J R Mendell, M I Periquet, et al.
Muscle & Nerve
|
May 20, 1999
Multifocal acquired demyelinating sensory and motor neuropathy: the Lewis-Sumner syndrome
D S Saperstein, A A Amato, G I Wolfe, et al.
Archives of Neurology
|
February 1, 1994
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorder
E Tan, D J Lynn, A A Amato, et al.
Page
of 12