Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Carmen Barbadillo Mateos"'
Autor:
Juan Carlos López-Robledillo, Patricia Carreira, Valentina Maldonado-Romero, Paloma García de la Peña Lefebvre, Henry Moruno-Cruz, Beatriz Joven, Tatiana Cobo-Ibáñez, Irene Llorente Cubas, Lucía Ruiz-Gutiérrez, Francisco Javier López-Longo, L. Lojo, María Carmen Barbadillo-Mateos, Eva Tomero, Ana Fernández Pérez, María Jesús García de Yébenes, Carmen Larena-Grijalba, Raquel Almodóvar González, Laura Nuño-Nuño
Publikováno v:
Rheumatology International. 37:1853-1861
The present study was undertaken to assess mortality, causes of death, and associated prognostic factors in a large cohort of patients diagnosed with idiopathic inflammatory myositis (IIM) from Spain. A retrospective longitudinal study was carried ou
Autor:
Carolina Merino Argumánez, José Luis Andreu Sánchez, María Espinosa, Hilda Godoy, Consuelo Ramos Giráldez, Carmen Barbadillo Mateos, Olga Rusinovich
Publikováno v:
Abstracts accepted for Publication.
Background: Gastric angiodysplasia and the typical “watermelon stomach” aspect is one of the most characteristic vascular manifestations in systemic sclerosis (SS). These angiodysplasias can affect the intestine ocasionally as well as the stomach
Autor:
Consuelo Ramos Giráldez, María Espinosa, Carolina Merino Argumánez, Carmen Barbadillo Mateos, José Luis Andreu Sánchez, Olga Rusinovich, Fernando León Vázquez, Patricia Fernández Crespo
Publikováno v:
Abstracts Accepted for Publication.
Background: The time of rheumatoid arthritis (RA) evolution until treatment begins is key to controlling the disease. Many studies have shown that a prolonged duration of symptoms at the onset of treatment is associated with a more severe course of R
Autor:
Luis Fernando Villa Alcázar, Carolina Merino Argumánez, Consuelo Ramos Giráldez, María Espinosa, Carmen Barbadillo Mateos, Jose Campos Esteban, Carlos Isasi Zaragoza, Hilda Godoy, Jesús Sanz, Olga Rusinovich, Mónica Fernández Castro, José Luis Andreu Sánchez, Mercedes Jiménez Palop
Publikováno v:
Abstracts Accepted for Publication.
Background: Belimumab is a human IgG1l monoclonal antibody directed against BAFF, a B lymphocyte survival factor. It is indicated as adjuvant treatment in adult patients with active systemic lupus erythematosus (SLE), with positive autoantibodies and
Autor:
Valentina Maldonado-Romero, Raquel Almodóvar, Lucía Ruiz-Gutiérrez, L. Lojo, Patricia Carreira, Paloma García de la Peña Lefebvre, Carmen Larena-Grijalba, Henry Moruno-Cruz, Ana Fernández Pérez, Laura Nuño-Nuño, María Jesús García de Yébenes, Eva Tomero, Francisco Javier López-Longo, María Carmen Barbadillo-Mateos, Irene Llorente Cubas, Juan Carlos López-Robledillo, Beatriz Joven, Tatiana Cobo-Ibáñez
Publikováno v:
International Journal of Rheumatic Diseases.
Background: Inflammatory idiopathic myositis (IIM) comprises a heterogeneous group of systemic muscular diseases that can occur together with other connective tissue diseases (CTD), named overlap myositis (OM). The question of whether OM is a distinc
Autor:
Consuelo Ramos Giráldez, Ana Royuela Vicente, Jose Campos Esteban, Carlos Isasi Zaragoza, José Luis Andreu Sánchez, Marta Isabel Sanz Pérez, Robert Francis Andrus, Abel Alejandro Sanabria Sanchinel, Mercedes Jiménez Palop, Juan Mulero Mendoza, Carolina Merino Argumánez, Luis Fernando Villa Alcázar, Carmen Barbadillo Mateos, María Espinosa Malpartida, Jesús Sanz Sanz, Hildegarda Godoy Tundidor, Bryan Josué Flores-Robles
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
instname
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Objective The aim of this study was to compare the functional results of 2 different procedure types, medical or surgical used in treating native joint septic arthritis. Methods In this cohort study, we reviewed the clinical registries of patients ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad943637944e74e275acdecbb0663b05
https://doi.org/10.1097/rhu.0000000000000615
https://doi.org/10.1097/rhu.0000000000000615
Autor:
Valentina Maldonado-Romero, Laura Barrio Nogal, Juan Carlos López-Robledillo, Irene Llorente Cubas, Francisco-Javier López-Longo, Patricia Carreira, Raquel Almodóvar, Carmen Larena-Grijalba, L. Lojo, Beatriz Joven, Tatiana Cobo-Ibáñez, Lucía Ruiz-Gutiérrez, Laura Nuño-Nuño, Carmen Barbadillo Mateos, Santiago Muñoz-Fernández, Ana Fernández Pérez, Alejandro Gómez-Gómez, María Jesús García de Yébenes, Paloma García de la Peña Lefebvre, Eva Tomero Muriel
Publikováno v:
Clinical rheumatology. 38(3)
Objective: To study prognostic factors in different types of idiopathic inflammatory myopathies (IIM) associated with interstitial lung disease (ILD). Patients and methods: Multicenter retrospective study of a Spanish cohort of patients diagnosed wit
Autor:
Carmen Larena-Grijalba, Ariel Perez Perez, Lucía Ruiz-Gutiérrez, R. Almodóvar González, María Carmen Barbadillo-Mateos, Eva Tomero, Juan Carlos López-Robledillo, Patricia Carreira, P. García de la Peña Lefebvre, Laura Nuño, Henry Moruno-Cruz, Beatriz Joven, Tatiana Cobo-Ibáñez, M.J. García-de Yébenes, Valentina Maldonado-Romero, L. Lojo, J. Martínez Barrio, I. Llorente Cubas, Francisco Javier López-Longo
Publikováno v:
FRIDAY, 15 JUNE 2018.
Background Among the subtypes of idiopathic inflammatory myopathy (IIM), it has been recognised that primary polymyositis (PM) and primary dermatomyositis (DM) have a worse prognosis than overlap syndrome (OM). However, the benign course of OM has no
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Carmen Barbadillo Mateos, Clara Sangüesa Gómez, María Espinosa Malpartida, Beatriz Jara Chinarro, Bryan Josué Flores Robles
Publikováno v:
Reumatología Clínica (English Edition). 12:345-347
Pulmonary involvement in the form of acute pneumonitis in adult-onset Still's disease (AOSD) is an uncommon manifestation, with few cases reported in the literature. We report the case of a 61-year-old male with 3 years of AOSD evolution, treated wit