Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ester Tobias-Baraja"'
Autor:
Iago Pinal-Fernandez, Angela Quintana, Jose Cesar Milisenda, Maria Casal-Dominguez, Sandra Muñoz-Braceras, Assia Derfoul, Jiram Torres-Ruiz, Katherine Pak, Stefania Dell'Orso, Faiza Naz, Gustavo Gutierrez-Cruz, Margherita Milone, Shahar Shelly, Yaiza Duque-Jaimez, Ester Tobias-Baraja, Ana Matas-Garcia, Gloria Garrabou, Joan Padrosa, Javier Ros, Ernesto Trallero-Araguás, Brian Walitt, Lisa Christopher-Stine, Thomas E Lloyd, Chen Zhao, Shannon Swift, Arun Rajan, Josep Maria Grau-Junyent, Albert Selva-O'Callaghan, Teerin Liewluck, Andrew Lee Mammen
Publikováno v:
Annals of the Rheumatic Diseases. 82:829-836
ObjectivesInflammatory myopathy or myositis is a heterogeneous family of immune-mediated diseases including dermatomyositis (DM), antisynthetase syndrome (AS), immune-mediated necrotising myopathy (IMNM) and inclusion body myositis (IBM). Immune chec
Autor:
Iago Pinal-Fernandez, Angela Quintana, Jose C. Milisenda, Maria Casal-Dominguez, Sandra Muñoz-Braceras, Assia Derfoul, Jiram Torres-Ruiz, Katherine Pak, Stefania Del Orso, Faiza Naz, Gustavo Gutierrez-Cruz, Margherita Milone, Shahar Shelly, Yaiza Duque-Jaimez, Ester Tobias-Baraja, Ana Matas-Garcia, Gloria Garrabou, Joan Padrosa, Javier Ros, Ernesto Trallero-Araguás, Brian Walitt, Lisa Christopher-Stine, Thomas E. Lloyd, Chen Zhao, Shannon Swift, Arun Rajan, Josep Maria Grau, Albert Selva-O’Callaghan, Teerin Liewluck, Andrew L. Mammen
ObjectivesInflammatory myopathy or myositis is a heterogeneous family of immune-mediated diseases including dermatomyositis (DM), antisynthetase syndrome (AS), immune-mediated necrotizing myopathy (IMNM), and inclusion body myositis (IBM). Immune che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0e51a0338d822551f4edb1396c23f81
https://doi.org/10.1101/2022.12.12.520136
https://doi.org/10.1101/2022.12.12.520136
Autor:
Noura Abdalla, Ester Tobías-Baraja, Alejandro Gonzalez, Gloria Garrabou, Gustavo Egea, Victoria Campuzano
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10071 (2023)
Williams–Beuren syndrome (WBS) is a rare neurodevelopmental disorder that, together with a rather characteristic neurocognitive profile, presents a strong cardiovascular phenotype. The cardiovascular features of WBS are mainly related to a gene dos
Externí odkaz:
https://doaj.org/article/6d1ae4da82b840238b68390a5418a854