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Neuropathology and Applied Neurobiology
|
April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathy
M Cerino, E Campana-Salort, A Salvi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
N Deconinck, P Richard, V Allamand, et al.
Revue Neurologique
|
December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]
J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique
|
September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]
M Renouil, T Stojkovic, M L Jacquemont, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Journal of Neurology
|
September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations
N C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Journal of Neurology
|
December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
A Ben Ammar, F Petit, N Alexandri, et al.
Muscle & Nerve
|
April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study
Alexandre Guérémy, V Morel, T Stojkovic, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 121) with videos related to
Sort By:
Page
of 13
Neuropathology and Applied Neurobiology
|
April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathy
M Cerino, E Campana-Salort, A Salvi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
N Deconinck, P Richard, V Allamand, et al.
Revue Neurologique
|
December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]
J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique
|
September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]
M Renouil, T Stojkovic, M L Jacquemont, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Journal of Neurology
|
September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations
N C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Journal of Neurology
|
December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
A Ben Ammar, F Petit, N Alexandri, et al.
Muscle & Nerve
|
April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study
Alexandre Guérémy, V Morel, T Stojkovic, et al.
Page
of 13