Evidence of muscle loss delay and improvement of hyperinsulinemia and insulin resistance in Duchenne muscular dystrophy supplemented with omega-3 fatty acids: A randomized study

Author:

Rodríguez-Cruz MaricelaORCID,Atilano-Miguel Salvador,Barbosa-Cortés Lourdes,Bernabé-García Mariela,Almeida-Becerril Tomas,Cárdenas-Conejo Alan,del Rocío Cruz-Guzmán Oriana,Maldonado-Hernández Jorge

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Elsevier BV

Subject

Critical Care and Intensive Care Medicine,Nutrition and Dietetics

Reference42 articles.

1. Diagnosis and management of Duchenne muscular dystrophy. Part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management;Birnkrant;Lancet Neurol,2018

2. Muscular dystrophies and the dystrophin-glycoprotein complex;Straub;Curr Opin Neurol,1997

3. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on Hind III and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations;Darras;Am J Hum Genet,1988

4. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene;Gillard;Am J Hum Genet,1989

5. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion ‘‘hot spot’’ region;Coral-Vázquez;Am J Med Genet,1997

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