Genetic modifiers of respiratory function in Duchenne muscular dystrophy

OBJECTIVE: Respiratory insufficiency is a major complication of Duchenne muscular dystrophy (DMD). Its progression shows considerable interindividual variability, which has been less thoroughly characterized and understood than in skeletal muscle. We collected pulmonary function testing (PFT) data f...

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Detalhes bibliográficos
Publicado no:Ann Clin Transl Neurol
Main Authors: Bello, Luca, D’Angelo, Grazia, Villa, Matteo, Fusto, Aurora, Vianello, Sara, Merlo, Beatrice, Sabbatini, Daniele, Barp, Andrea, Gandossini, Sandra, Magri, Francesca, Comi, Giacomo P., Pedemonte, Marina, Tacchetti, Paola, Lanzillotta, Valentina, Trucco, Federica, D’Amico, Adele, Bertini, Enrico, Astrea, Guja, Politano, Luisa, Masson, Riccardo, Baranello, Giovanni, Albamonte, Emilio, De Mattia, Elisa, Rao, Fabrizio, Sansone, Valeria A., Previtali, Stefano, Messina, Sonia, Vita, Gian Luca, Berardinelli, Angela, Mongini, Tiziana, Pini, Antonella, Pane, Marika, Mercuri, Eugenio, Vianello, Andrea, Bruno, Claudio, Hoffman, Eric P., Morgenroth, Lauren, Gordish‐Dressman, Heather, McDonald, Craig M., Pegoraro, Elena
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7261745/
https://ncbi.nlm.nih.gov/pubmed/32343055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51046
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