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Neuromuscular Disorders : NMD
|
December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathies
S Quijano-Roy, S Khirani, M Colella, et al.
Neurology
|
July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation
A Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
Brain : a Journal of Neurology
|
November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
D Hicks, A K Lampe, S H Laval, et al.
Journal of Neuroengineering and Rehabilitation
|
October 16, 2024
Acceptability, validity and responsiveness of inertial measurement units for assessing motor recovery after gene therapy in infants with early onset spinal muscular atrophy: a prospective cohort study
R Barrois, B Tervil, M Cacioppo, et al.
Neurology
|
October 7, 2009
Core-rod myopathy caused by mutations in the nebulin gene
N B Romero, V-L Lehtokari, S Quijano-Roy, et al.
Neuromuscular Disorders : NMD
|
December 11, 2012
Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients
L Servais, N Deconinck, A Moraux, 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.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
April 26, 2016
A penicillin- and metronidazole-resistant Clostridium botulinum strain responsible for an infant botulism case
C Mazuet, E-J Yoon, S Boyer, et al.
Neuromuscular Disorders : NMD
|
March 7, 2023
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapy
R Barrois, C Barnerias, E Deladrière, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands
F Muntoni, E Bertini, C Bönnemann, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Neuromuscular Disorders : NMD
|
December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathies
S Quijano-Roy, S Khirani, M Colella, et al.
Neurology
|
July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation
A Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
Brain : a Journal of Neurology
|
November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
D Hicks, A K Lampe, S H Laval, et al.
Journal of Neuroengineering and Rehabilitation
|
October 16, 2024
Acceptability, validity and responsiveness of inertial measurement units for assessing motor recovery after gene therapy in infants with early onset spinal muscular atrophy: a prospective cohort study
R Barrois, B Tervil, M Cacioppo, et al.
Neurology
|
October 7, 2009
Core-rod myopathy caused by mutations in the nebulin gene
N B Romero, V-L Lehtokari, S Quijano-Roy, et al.
Neuromuscular Disorders : NMD
|
December 11, 2012
Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients
L Servais, N Deconinck, A Moraux, 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.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
April 26, 2016
A penicillin- and metronidazole-resistant Clostridium botulinum strain responsible for an infant botulism case
C Mazuet, E-J Yoon, S Boyer, et al.
Neuromuscular Disorders : NMD
|
March 7, 2023
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapy
R Barrois, C Barnerias, E Deladrière, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands
F Muntoni, E Bertini, C Bönnemann, et al.
Page
of 3