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Identification of mutations on the EMD and EYA4 genes associated with Emery–Dreifuss muscular dystrophy and deafness: a case report
ArticleAbstract: Introduction: Hearing loss is the most common sensory disability, and it is estimated that 50% of caPalabras claves:Case report, Deafness, genome, Muscular dystrophy, NGSAutores:Alexandra Patricia Guevara, Ana Karina Zambrano, Doménech N., Elius Andrés Paz Cruz, Ibarra-Castillo R., Ibarra-Rodríguez A.A., Laso-Bayas J.L., Rafael Tamayo Trujillo, Ricardo Hidalgo-Ottolenghi, Santiago André Cadena Ullauri, VIVIANA ALEJANDRA RUIZ POZOFuentes:orcidscopusUnlocking the potential: very-low-energy ketogenic therapy in obesity-related disorders
ReviewAbstract: The Very Low-Energy Ketogenic Therapy (VLEKT) is a structured, multi-phase dietary regimen characterPalabras claves:cardiovascular diseases, Chronic Diseases, good health and well-being, Obesity-related disorders, Very-Low-Energy Ketogenic Therapy, VLEKTAutores:Ana Karina Zambrano, Angelo Michele Carella, Claudia Reytor-González, Claudia V. Guerra, Daniel Simancas-Racines, Frias Toral Evelyn, Giuseppe Annunziata, Ricardo Hidalgo-Ottolenghi, Verde L.Fuentes:orcidscopus