Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study.

Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic. Journal of

Table 3 — Results of electromyographies and muscle biopsies grouped according to the pathology: PHMD, pseudo­hypertrophic muscular dystrophy; LGMD, limb­girdle muscular dystrophy

Normal and dystrophin deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.. Comi G, Comola M,

Objective: To assess the evolution of motor function in patients with Duchenne muscular dystrophy (DMD) treated with steroids (predni- solone or deflazacort) through the Motor

Objective: The relationship between functional dependence and quality of life (QOL) in Duchenne muscular dystrophy (DMD) patients and burden and QOL in caregivers is not clear..

Dystrophin, which is usually distributed in the subsarco- lemmal zone of skeletal muscle fibers, is absent in Duchenne muscular dystrophy (DMD) and present in variable amounts with

In addition to a lack of dystrophin, studies are emerging that are painting a picture of a more intricate connection between mitochondrial dysfunction and DMD where increased

Dystrophin expression in muscles of duchenne muscular dystrophy patients after high-density injections of normal myogenic cells. Viral vectors in gene