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European Journal of Neurology
|
January 5, 2011
Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases
S Larue, F Bombelli, K Viala, et al.
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.
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.
American Journal of Human Genetics
|
June 10, 2000
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene
V Delague, C Bareil, S Tuffery, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
April 20, 2019
Sarcoidosis occurring during BRAF/MEK inhibitors is associated with paradoxical ERK activation in Erdheim-Chester patients
A Amoura, J Haroche, J-F Emile, et al.
Revue Neurologique
|
April 8, 2020
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults
Y Nadjar, S Souvannanorath, T Maisonobe, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
N Le Forestier, T Maisonobe, A Piquard, et al.
International Journal of Clinical Practice
|
August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey
O Lidove, U Ramaswami, R Jaussaud, et al.
Brain : a Journal of Neurology
|
May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A
D Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 122) with videos related to
Sort By:
Page
of 13
European Journal of Neurology
|
January 5, 2011
Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases
S Larue, F Bombelli, K Viala, et al.
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.
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.
American Journal of Human Genetics
|
June 10, 2000
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene
V Delague, C Bareil, S Tuffery, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
April 20, 2019
Sarcoidosis occurring during BRAF/MEK inhibitors is associated with paradoxical ERK activation in Erdheim-Chester patients
A Amoura, J Haroche, J-F Emile, et al.
Revue Neurologique
|
April 8, 2020
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults
Y Nadjar, S Souvannanorath, T Maisonobe, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
N Le Forestier, T Maisonobe, A Piquard, et al.
International Journal of Clinical Practice
|
August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey
O Lidove, U Ramaswami, R Jaussaud, et al.
Brain : a Journal of Neurology
|
May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A
D Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Page
of 13