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Journal of the Neurological Sciences
|
April 20, 2001
Primary lateral sclerosis: further clarification
N Le Forestier, T Maisonobe, L Spelle, et al.
Revue Neurologique
|
May 5, 2000
[What's new in primary lateral sclerosis?]
N Le Forestier, T Maisonobe, L Spelle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1995
Multifocal motor neuropathy with conduction block: a study of 24 patients
P Bouche, A Moulonguet, A B Younes-Chennoufi, et al.
Revue Medicale De Liege
|
July 13, 2004
[The hypolossal-facial anastomosis in man. A model for studying peripheral and central nervous system plasticity]
F Tankéré, I Bernat, E Vitte, et al.
Neuromuscular Disorders : NMD
|
September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene
E Le Guern, N Ravise, M Gugenheim, et al.
Human Molecular Genetics
|
January 1, 1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
E LeGuern, R Gouider, N Ravisé, et al.
Neurology
|
December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities
R Gouider, E LeGuern, J Emile, et al.
American Journal of Human Genetics
|
June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
J Lopes, E LeGuern, R Gouider, et al.
Neurology
|
April 23, 2003
Interferon beta-1a as an investigational treatment for CIDP
J-M Vallat, A F Hahn, J-M Léger, et al.
Supplements to Clinical Neurophysiology
|
August 19, 2010
Motor neuron disorders: novel electrophysiologic approach (MUFDEC protocol)
F C Wang, N Le Forestier, P Gérard, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 158) with videos related to
Sort By:
Page
of 16
Journal of the Neurological Sciences
|
April 20, 2001
Primary lateral sclerosis: further clarification
N Le Forestier, T Maisonobe, L Spelle, et al.
Revue Neurologique
|
May 5, 2000
[What's new in primary lateral sclerosis?]
N Le Forestier, T Maisonobe, L Spelle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1995
Multifocal motor neuropathy with conduction block: a study of 24 patients
P Bouche, A Moulonguet, A B Younes-Chennoufi, et al.
Revue Medicale De Liege
|
July 13, 2004
[The hypolossal-facial anastomosis in man. A model for studying peripheral and central nervous system plasticity]
F Tankéré, I Bernat, E Vitte, et al.
Neuromuscular Disorders : NMD
|
September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene
E Le Guern, N Ravise, M Gugenheim, et al.
Human Molecular Genetics
|
January 1, 1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
E LeGuern, R Gouider, N Ravisé, et al.
Neurology
|
December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities
R Gouider, E LeGuern, J Emile, et al.
American Journal of Human Genetics
|
June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
J Lopes, E LeGuern, R Gouider, et al.
Neurology
|
April 23, 2003
Interferon beta-1a as an investigational treatment for CIDP
J-M Vallat, A F Hahn, J-M Léger, et al.
Supplements to Clinical Neurophysiology
|
August 19, 2010
Motor neuron disorders: novel electrophysiologic approach (MUFDEC protocol)
F C Wang, N Le Forestier, P Gérard, et al.
Page
of 16