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The Journal of Cell Biology
|
September 23, 1998
Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice
F Duclos, V Straub, S A Moore, et al.
Neuromuscular Disorders : NMD
|
March 11, 2019
Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre study
V Ricotti, V Selby, D Ridout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK
S Figueroa-Bonaparte, J Hudson, R Barresi, 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.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
Human Molecular Genetics
|
December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
M Brockington, Y Yuva, P Prandini, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Human Mutation
|
March 28, 2008
Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance
A K Lampe, Y Zou, D Sudano, et al.
Neuromuscular Disorders : NMD
|
August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)
F Muntoni, B Valero de Bernabe, R Bittner, et al.
Acta Neuropathologica
|
January 4, 2020
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern
E Servián-Morilla, M Cabrera-Serrano, K Johnson, et al.
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of 10
Search research articles
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Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
The Journal of Cell Biology
|
September 23, 1998
Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice
F Duclos, V Straub, S A Moore, et al.
Neuromuscular Disorders : NMD
|
March 11, 2019
Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre study
V Ricotti, V Selby, D Ridout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK
S Figueroa-Bonaparte, J Hudson, R Barresi, 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.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
Human Molecular Genetics
|
December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
M Brockington, Y Yuva, P Prandini, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Human Mutation
|
March 28, 2008
Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance
A K Lampe, Y Zou, D Sudano, et al.
Neuromuscular Disorders : NMD
|
August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)
F Muntoni, B Valero de Bernabe, R Bittner, et al.
Acta Neuropathologica
|
January 4, 2020
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern
E Servián-Morilla, M Cabrera-Serrano, K Johnson, et al.
Page
of 10