Pharmacotherapy of Muscle Dystrophies

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmacology".

Deadline for manuscript submissions: closed (30 November 2023) | Viewed by 346

Special Issue Editor


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Guest Editor
Translational Genomics Group, Biology Faculty, University of Valencia, 46100 Burjassot, Spain
Interests: rare disease; drug development; science; genetics

Special Issue Information

Dear Colleagues,

Muscular dystrophies involve a large list of primary diseases due to mutations in more than 70 specific genes, which result in the observation of dystrophic changes in different muscles. In other words, degenerated muscle is usually replaced by fibrous tissues unable to perform normal muscle function. Importantly, in several cases, is not only the skeletal muscle affected, but also other tissues, such as the heart, eyes, spine, endocrine glands, brain, etc. Given the numerous genetic defects identified today, as well as our improved understanding of the pathogenesis of some of these diseases, novel therapeutic approaches have been developed. From the large list of muscular dystrophy diseases, only Duchenne muscular dystrophy has recently achieved approval for a few personalized therapies, with the rest of the diseases in different position through the drug development pathway. In this Special Issue, we concentrate on assembling examples of therapeutic opportunities and developments for some of the diseases into the group of muscular dystrophy conditions.

This Special Issue of Pharmaceuticals, entitled “Pharmacotherapy of Muscle Dystrophies”, will cover a selection of research topics related to recent advances in the mechanisms of muscular dystrophies, as well as novel therapeutic approaches. Experimental papers, commentaries, and up-to-date review articles are all welcome.

Dr. Arturo López Castel
Guest Editor

Manuscript Submission Information

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Keywords

  • muscular dystrophy
  • therapy
  • skeletal muscle
  • pharmacologic development

Published Papers

There is no accepted submissions to this special issue at this moment.
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