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Journal De Radiologie
|
January 19, 2011
[Imaging features of neurologic and orthopedic complications from severe trauma]
J Ezra, F Roffi, F Eichwald, et al.
Revue Neurologique
|
January 10, 2022
Nusinersen treatment in adults with severe spinal muscular atrophy: A real-life retrospective observational cohort study
C Lefeuvre, M Brisset, M Sarlon, et al.
Neuromuscular Disorders : NMD
|
December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathies
S Quijano-Roy, S Khirani, M Colella, et al.
La Revue De Medecine Interne
|
January 8, 2011
[Enzyme replacement therapy of lysosomal storage diseases]
D P Germain, C Boucly, R Y Carlier, et al.
Neuromuscular Disorders : NMD
|
January 31, 2009
Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype
S Vuillaumier-Barrot, S Quijano-Roy, C Bouchet-Seraphin, 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
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
Journal De Radiologie
|
January 19, 2011
[Imaging features of neurologic and orthopedic complications from severe trauma]
J Ezra, F Roffi, F Eichwald, et al.
Revue Neurologique
|
January 10, 2022
Nusinersen treatment in adults with severe spinal muscular atrophy: A real-life retrospective observational cohort study
C Lefeuvre, M Brisset, M Sarlon, et al.
Neuromuscular Disorders : NMD
|
December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathies
S Quijano-Roy, S Khirani, M Colella, et al.
La Revue De Medecine Interne
|
January 8, 2011
[Enzyme replacement therapy of lysosomal storage diseases]
D P Germain, C Boucly, R Y Carlier, et al.
Neuromuscular Disorders : NMD
|
January 31, 2009
Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype
S Vuillaumier-Barrot, S Quijano-Roy, C Bouchet-Seraphin, 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
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 3