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Neuromuscular Disorders : NMD
|
January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus
L Hartley, M Kinali, R Knight, et al.
Neurology
|
July 1, 2009
Natural history of Ullrich congenital muscular dystrophy
A Nadeau, M Kinali, M Main, et al.
Muscle & Nerve
|
March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
E Mercuri, S C Brown, P Nihoyannopoulos, et al.
Neuromuscular Disorders : NMD
|
August 19, 2003
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype
E Mercuri, C Cini, A Pichiecchio, et al.
Human Gene Therapy
|
September 5, 2007
Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle
V Arechavala-Gomeza, I R Graham, L J Popplewell, et al.
Neuropediatrics
|
August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxity
E Mercuri, A Lampe, V Straub, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycan
F Muntoni, M Brockington, C Godfrey, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E Mercuri, E Bertini, S Messina, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Neuromuscular Disorders : NMD
|
January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus
L Hartley, M Kinali, R Knight, et al.
Neurology
|
July 1, 2009
Natural history of Ullrich congenital muscular dystrophy
A Nadeau, M Kinali, M Main, et al.
Muscle & Nerve
|
March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
E Mercuri, S C Brown, P Nihoyannopoulos, et al.
Neuromuscular Disorders : NMD
|
August 19, 2003
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype
E Mercuri, C Cini, A Pichiecchio, et al.
Human Gene Therapy
|
September 5, 2007
Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle
V Arechavala-Gomeza, I R Graham, L J Popplewell, et al.
Neuropediatrics
|
August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxity
E Mercuri, A Lampe, V Straub, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycan
F Muntoni, M Brockington, C Godfrey, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E Mercuri, E Bertini, S Messina, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Page
of 3