Results 111 to 120 of about 4,506 (155)

Clinical Trial Readiness in Limb Girdle Muscular Dystrophy R1 (LGMDR1): A GRASP Consortium Study. [PDF]

open access: yesAnn Clin Transl Neurol
Hunn SM   +29 more
europepmc   +1 more source

Progress on cell therapy for skeletal muscle disorders. [PDF]

open access: yesAdv Drug Deliv Rev
Azzag K, Perlingeiro RCR.
europepmc   +1 more source

Expanding the Clinico-Genetic Scope of Bethlem Myopathy: A Family of Five Patients from Kerala. [PDF]

open access: yesAnn Indian Acad Neurol
Saibaba J   +4 more
europepmc   +1 more source

A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy. [PDF]

open access: yesBMC Med Genomics
Nejati P   +6 more
europepmc   +1 more source

DAB2 in LGMD R2: a molecular link between disease progression and lipid dysregulation. [PDF]

open access: yesJCI Insight
Bruge C   +16 more
europepmc   +1 more source

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