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Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Revue Neurologique
|
April 5, 2023
Current clinical management of CIDP with immunoglobulins in France: An expert opinion
P Cintas, F Bouhour, C Cauquil, et al.
Neurology
|
October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA
M Mancuso, L Salviati, S Sacconi, 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
|
July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging
G Giacomucci, M Monforte, J Diaz-Manera, et al.
Neurology
|
October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2
J C de Greef, R J L F Lemmers, P Camaño, et al.
Neurology
|
August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1
I Pénisson-Besnier, M Devillers, R Porcher, 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.
Annals of the Rheumatic Diseases
|
January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis
J B Lilleker, A Rietveld, S R Pye, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Revue Neurologique
|
April 5, 2023
Current clinical management of CIDP with immunoglobulins in France: An expert opinion
P Cintas, F Bouhour, C Cauquil, et al.
Neurology
|
October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA
M Mancuso, L Salviati, S Sacconi, 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
|
July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging
G Giacomucci, M Monforte, J Diaz-Manera, et al.
Neurology
|
October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2
J C de Greef, R J L F Lemmers, P Camaño, et al.
Neurology
|
August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1
I Pénisson-Besnier, M Devillers, R Porcher, 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.
Annals of the Rheumatic Diseases
|
January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis
J B Lilleker, A Rietveld, S R Pye, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Page
of 4