Zobrazeno 1 - 10
of 43
pro vyhledávání: '"A. Trangulao"'
Autor:
Mathieu Cerino, Patricio González-Hormazábal, Mario Abaji, Sebastien Courrier, Francesca Puppo, Yves Mathieu, Alejandra Trangulao, Nicholas Earle, Claudia Castiglioni, Jorge Díaz, Mario Campero, Ricardo Hughes, Carmen Vargas, Rocío Cortés, Karin Kleinsteuber, Ignacio Acosta, J. Andoni Urtizberea, Nicolas Lévy, Marc Bartoli, Martin Krahn, Lilian Jara, Pablo Caviedes, Svetlana Gorokhova, Jorge A. Bevilacqua
Publikováno v:
Genes, Vol 13, Iss 6, p 1076 (2022)
Hereditary myopathies are a group of genetically determined muscle disorders comprising more than 300 entities. In Chile, there are no specific registries of the distinct forms of these myopathies. We now report the genetic findings of a series of Ch
Externí odkaz:
https://doaj.org/article/b6d4a30088a545e0b6883988fde21b16
Autor:
Carla Basualto-Alarcón, Félix A Urra, María Francisca Bozán, Fabián Jaña, Alejandra Trangulao, Jorge A Bevilacqua, J César Cárdenas
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0242443 (2020)
Idiopathic Inflammatory Myopathies (IIMs) have been studied within the framework of autoimmune diseases where skeletal muscle appears to have a passive role in the illness. However, persiting weakness even after resolving inflammation raises question
Externí odkaz:
https://doaj.org/article/8ac7220ddf364f8da39eff85fbfced1c
Autor:
Jorge A. Bevilacqua, Juan Pablo Contreras, Alejandra Trangulao, Úrsula Hernández, Guy Brochier, Jorge Díaz, Ricardo Hughes, Mario Campero, Norma B. Romero
Publikováno v:
Neuromuscular Disorders. 32:687-691
Akademický článek
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Autor:
Bevilacqua, Mathieu Cerino, Patricio González-Hormazábal, Mario Abaji, Sebastien Courrier, Francesca Puppo, Yves Mathieu, Alejandra Trangulao, Nicholas Earle, Claudia Castiglioni, Jorge Díaz, Mario Campero, Ricardo Hughes, Carmen Vargas, Rocío Cortés, Karin Kleinsteuber, Ignacio Acosta, J. Andoni Urtizberea, Nicolas Lévy, Marc Bartoli, Martin Krahn, Lilian Jara, Pablo Caviedes, Svetlana Gorokhova, Jorge A.
Publikováno v:
Genes; Volume 13; Issue 6; Pages: 1076
Hereditary myopathies are a group of genetically determined muscle disorders comprising more than 300 entities. In Chile, there are no specific registries of the distinct forms of these myopathies. We now report the genetic findings of a series of Ch
Autor:
Cerino, Mathieu, Gonzalez-Hormazabal, Patricio, Abaji, Mario, Courrier, Sebastien, Puppo, Francesca, Mathieu, Yves, Trangulao, Alejandra, Earle, Nicholas, Castiglioni, Claudia, Diaz, Jorge, Campero, Mario, Hughes, Ricardo, Vargas, Carmen, Cortes, Rocio, Kleinsteuber, Karin, Acosta, Ignacio, Urtizberea, J. Andoni, Levy, Nicolas, Bartoli, Marc, Krahn, Martin, Jara, Lilian, Caviedes, Pablo, Gorokhova, Svetlana, Bevilacqua, Jorge A.
Publikováno v:
Genes
Genes, 2022, 13 (6), ⟨10.3390/genes13061076⟩
Genes, 2022, 13 (6), ⟨10.3390/genes13061076⟩
International audience; Hereditary myopathies are a group of genetically determined muscle disorders comprising more than 300 entities. In Chile, there are no specific registries of the distinct forms of these myopathies. We now report the genetic fi
Publikováno v:
Neuromuscular Disorders. 31:1218-1219
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
A. Trangulao, María Francisca Bozán, Fabián Jaña, J César Cárdenas, Félix A. Urra, Jorge A. Bevilacqua, Carla Basualto-Alarcón
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 11, p e0242443 (2020)
PLoS ONE, Vol 15, Iss 11, p e0242443 (2020)
Idiopathic Inflammatory Myopathies (IIMs) have been studied within the framework of autoimmune diseases where skeletal muscle appears to have a passive role in the illness. However, persiting weakness even after resolving inflammation raises question
Autor:
A. Trangulao, Claudia Castiglioni, Mario Campero, Patricio Gonzalez-Hormazabal, Lisanne Woudt, Ricardo Hughes, Jon Andoni Urtizberea, Gabriella A. Di Capua, Jorge A. Bevilacqua, Lilian Jara, Martin Krahn, Raúl Godoy-Herrera, Nicolas Lévy
Publikováno v:
Muscle & Nerve. 53:49-57
Introduction Understanding the natural history of dysferlinopathy is essential to design and quantify novel therapeutic protocols. Our aim in this study was to assess, clinically and functionally, a cohort of patients with dysferlinopathy, using vali