Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Cristina Sabater-Abad"'
Autor:
Javier Narváez, Myriam Aburto, Daniel Seoane-Mato, Gema Bonilla, Orlando Acosta, Gloria Candelas, Esteban Cano-Jiménez, Iván Castellví, José María González-Ruiz, Héctor Corominas, Belén López-Muñiz, María Martín-López, Alejandro Robles-Pérez, Natalia Mena-Vázquez, José Antonio Rodríguez-Portal, Ana María Ortiz, Cristina Sabater-Abad, Isabel Castrejón, Raquel dos Santos, Sandra Garrote-Corral, Jesús Maese, Lucía Silva-Fernández, Santos Castañeda, Claudia Valenzuela
Publikováno v:
Reumatología Clínica. 19:74-81
Autor:
Javier Narváez, Myriam Aburto, Daniel Seoane-Mato, Gema Bonilla, Orlando Acosta, Gloria Candelas, Esteban Cano-Jiménez, Iván Castellví, José María González-Ruiz, Héctor Corominas, Belén López-Muñiz, María Martín-López, Alejandro Robles-Pérez, Natalia Mena-Vázquez, José Antonio Rodríguez-Portal, Ana María Ortiz, Cristina Sabater-Abad, Isabel Castrejón, Raquel dos Santos, Sandra Garrote-Corral, Jesús Maese, Lucía Silva-Fernández, Santos Castañeda, Claudia Valenzuela
Publikováno v:
Reumatología Clínica (English Edition). 19:74-81
To develop a joint proposal for screening criteria of interstitial lung disease (ILD) in patients with rheumatoid arthritis (RA) and vice versa, which serves as a guidelines in patient referral between the Rheumatology and Pneumology departments to e
Autor:
Estrella Fernández Fabrellas, Ricardo Peris Sánchez, Cristina Sabater Abad, Gustavo Juan Samper
Publikováno v:
Medical Sciences, Vol 6, Iss 2, p 51 (2018)
Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause, is the most common and deadly of the idiopathic interstitial pneumonias. With a median survival of 3–5 years following diagnosis, IP
Externí odkaz:
https://doaj.org/article/662dd21bbcf947ef9ddc80354b10003e
Autor:
Susana Torres, Esther Verdejo Mengual, Vanessa Jaimes Diaz, Silvia Calabuig, Gustavo Juan Samper, Estrella Fernández Fabrellas, Ignacio Martinez, Cristina Sabater Abad
Publikováno v:
Monitoring airway disease.
Autor:
Esther Verdejo Mengual, Susana Torres Martinez, Vanessa Jaimes Diaz, Gustavo Juan Samper, Estrella Fernández-Fabrellas, Cristina Sabater Abad, Silvia Calabuig Fariñas
Publikováno v:
Idiopathic interstitial pneumonias.
Autor:
Cristina Sabater Abad, Vicente Sabater Marco, Estrella Fernández Fabrellas, Gustavo Juan Samper
Publikováno v:
Revista Española de Patología. 51:257-261
Smoking-related interstitial fibrosis is a distinct form of fibrosis, found in smokers, which has striking histopathological features. We present a case of pulmonary interstitial fibrosis with cysts in a 58-year-old woman who was a significant active
Autor:
Jose María Huguet Malavés, Laura Larrey Ruiz, Cristina Sabater Abad, Laura Peño Muñoz, Gustavo Juan Samper
Publikováno v:
Archivos de Bronconeumología (English Edition). 55:108-110
Autor:
Jose María Huguet Malavés, Laura Peño Muñoz, Cristina Sabater Abad, Laura Larrey Ruiz, Gustavo Juan Samper
Publikováno v:
Archivos de Bronconeumología. 55:108-110
Autor:
Mercedes Ramón Capilla, Carola Guzmán Luján, Javier Milara Payá, Gustavo Juan Samper, Goitzane Marcaida Benito, Estrella Fernández Fabrellas, Cristina Sabater Abad, Raquel Rodriguez Lopez
Publikováno v:
Clinical Problems.
Autor:
Gustavo Juan Samper, Estrella Fernández Fabrellas, Cristina Sabater Abad, Ricardo Peris Sánchez
Publikováno v:
Medical Sciences
Medical Sciences, Vol 6, Iss 2, p 51 (2018)
Medical Sciences, Vol 6, Iss 2, p 51 (2018)
Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause, is the most common and deadly of the idiopathic interstitial pneumonias. With a median survival of 3–5 years following diagnosis, IP