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Clinical Neurology and Neurosurgery
|
January 3, 2012
Peripheral neuropathy and 46XY gonadal dysgenesis: confirmation of a heterogeneous entity
M Luigetti, S M Corsello, S Lattante, et al.
Journal of the Neurological Sciences
|
February 13, 2010
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia
M Luigetti, G Frisullo, L Laurenti, et al.
European Journal of Neurology
|
August 9, 2011
Immunosuppressive treatment in refractory chronic inflammatory demyelinating polyradiculoneuropathy. A nationwide retrospective analysis
D Cocito, S Grimaldi, I Paolasso, et al.
Clinical Neurology and Neurosurgery
|
June 12, 2010
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia
M Luigetti, A Modoni, R Renna, et al.
European Journal of Neurology
|
October 30, 2009
A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy
D Cocito, I Paolasso, G Antonini, et al.
Neurology
|
April 1, 1998
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)
A Gambardella, A Bolino, M Muglia, et al.
Journal of Neuroimmunology
|
June 1, 2010
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from multiple sclerosis, chronic inflammatory demyelinating polyradiculoneuropathy and amyotrophic lateral sclerosis
V Nociti, G Frisullo, A Marti, et al.
Neuromuscular Disorders : NMD
|
June 14, 2002
Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's disease
M Sabatelli, L Quaranta, F Madia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2010
Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature
L Benedetti, C Briani, D Franciotta, et al.
Neurology
|
May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 77) with videos related to
Sort By:
Page
of 8
Clinical Neurology and Neurosurgery
|
January 3, 2012
Peripheral neuropathy and 46XY gonadal dysgenesis: confirmation of a heterogeneous entity
M Luigetti, S M Corsello, S Lattante, et al.
Journal of the Neurological Sciences
|
February 13, 2010
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia
M Luigetti, G Frisullo, L Laurenti, et al.
European Journal of Neurology
|
August 9, 2011
Immunosuppressive treatment in refractory chronic inflammatory demyelinating polyradiculoneuropathy. A nationwide retrospective analysis
D Cocito, S Grimaldi, I Paolasso, et al.
Clinical Neurology and Neurosurgery
|
June 12, 2010
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia
M Luigetti, A Modoni, R Renna, et al.
European Journal of Neurology
|
October 30, 2009
A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy
D Cocito, I Paolasso, G Antonini, et al.
Neurology
|
April 1, 1998
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)
A Gambardella, A Bolino, M Muglia, et al.
Journal of Neuroimmunology
|
June 1, 2010
Epstein-Barr virus antibodies in serum and cerebrospinal fluid from multiple sclerosis, chronic inflammatory demyelinating polyradiculoneuropathy and amyotrophic lateral sclerosis
V Nociti, G Frisullo, A Marti, et al.
Neuromuscular Disorders : NMD
|
June 14, 2002
Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's disease
M Sabatelli, L Quaranta, F Madia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2010
Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature
L Benedetti, C Briani, D Franciotta, et al.
Neurology
|
May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, et al.
Page
of 8