Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sabrina Neves Silva"'
Autor:
Pedro Renato Chocair, Sara Mohrbacher, Precil Diego Miranda de Menezes Neves, Leonardo Victor Barbosa Pereira, Erico Souza Oliveira, Luciana Loureiro Nardotto, Alessandra Martins Bales, Victor Augusto Hamamoto Sato, Sabrina Neves Silva, Bernadete Maria Coelho Ferreira, Américo Lourenço Cuvello-Neto
Publikováno v:
BMC Geriatrics, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background McArdle disease is a myopathy caused by mutations in PYGM gene that is characterized by reduced or absent activity of myophosphorylase. Reports of patients with concomitant McArdle disease and diabetes are scarce. We report a case
Externí odkaz:
https://doaj.org/article/37934a4a833447f29c3dbddcbf71f6c5
Autor:
Erico Souza Oliveira, Luciana Loureiro Nardotto, Américo Lourenço Cuvello-Neto, Sabrina Neves Silva, Leonardo Victor Barbosa Pereira, Sara Mohrbacher, Victor Augusto Hamamoto Sato, Pedro R. Chocair, Bernadete Maria Coelho Ferreira, Alessandra Martins Bales, Precil Diego Miranda de Menezes Neves
Publikováno v:
BMC Geriatrics, Vol 20, Iss 1, Pp 1-6 (2020)
BMC Geriatrics
BMC Geriatrics
Background McArdle disease is a myopathy caused by mutations in PYGM gene that is characterized by reduced or absent activity of myophosphorylase. Reports of patients with concomitant McArdle disease and diabetes are scarce. We report a case of a pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e40b39c02a3304be15799c27e9873342
https://doi.org/10.1186/s12877-020-01812-4
https://doi.org/10.1186/s12877-020-01812-4