Results 301 to 310 of about 182,997 (357)

SURGICAL PROCEDURES PROLONG AMBULATION IN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY. [PDF]

open access: yesActa Ortop Bras
Nordon DG   +5 more
europepmc   +1 more source

Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy. [PDF]

open access: yesJ Clin Invest
Bengoechea R   +9 more
europepmc   +1 more source

Balanced Translocations Involving the <i>DMD</i> Gene as a Cause of Muscular Dystrophy in Female Children: A Description of Three Cases. [PDF]

open access: yesInt J Mol Sci
Vorontsova EO   +18 more
europepmc   +1 more source

Generation and characterization of a mouse model of Becker muscular dystrophy with a deletion of Dmd exons 52 to 55.

open access: yesDis Model Mech
Perillat LOM   +9 more
europepmc   +1 more source

The muscular dystrophies [PDF]

open access: possibleSeminars in Neurology, 2012
The muscular dystrophies are a group of inherited disorders that are clinically and genetically distinct. Genetic counselling is an essential part of the management of these patients. Molecular genetic techniques, in particular positional cloning but also now candidate gene analysis, have allowed the beginning of an understanding of the molecular ...
Kate Bushby, Una-Marie Sheerin
openaire   +5 more sources

The Muscular Dystrophies

New England Journal of Medicine, 1965
ABIOTROPHY of skeletal muscle — that is, degeneration and atrophy after a latent period of apparently normal development and function — is the most obvious common denominator in the group of disorders called the muscular dystrophies. It should be realized, however, that systems other than skeletal muscle are frequently involved in these diseases ...
Wayne S. Zundel, Frank H. Tyler
openaire   +4 more sources

Muscular dystrophies

The Lancet, 2013
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical features and dystrophic changes on muscle biopsy. An improved understanding of their molecular bases has led to more accurate definitions of the clinical features associated with known subtypes.
Mercuri, Eugenio Maria, Muntoni, F.
openaire   +5 more sources

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