Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Eduardo L. Callejas Moraga"'
Autor:
Alfredo Guillén-Del-Castillo, Carmen Pilar Simeón-Aznar, Eduardo L. Callejas-Moraga, Carles Tolosa-Vilella, Serafín Alonso-Vila, Vicente Fonollosa-Pla, Albert Selva-O’Callaghan
Publikováno v:
Arthritis Research & Therapy, Vol 20, Iss 1, Pp 1-10 (2018)
Abstract Background To determine whether lung involvement is related to microvascular perturbations, nailfold videocapillaroscopy (NVC) was performed in patients with systemic sclerosis (SSc). Methods A cross-sectional study was consecutively accompl
Externí odkaz:
https://doaj.org/article/574ce279a7b8443c9327c6ace1509c20
Autor:
Alfredo Guillén-Del Castillo, Eduardo L. Callejas-Moraga, Gabriela García, José F. Rodríguez-Palomares, Antonio Román, Cristina Berastegui, Manuel López-Meseguer, Enric Domingo, Vicente Fonollosa-Plá, Carmen Pilar Simeón-Aznar
Publikováno v:
Arthritis Research & Therapy, Vol 19, Iss 1, Pp 1-10 (2017)
Abstract Background Pulmonary arterial hypertension (PAH) is one of the most relevant causes of death in systemic sclerosis. The aims of this study were to analyse the recently published DETECT algorithm comparing it with European Society of Cardiolo
Externí odkaz:
https://doaj.org/article/1fea2ca8ad92419e91786059e7121159
Autor:
Michael Mahler, Karen Lorite-Gomez, Adriana Severino, V. Fonollosa-Pla, Maria Teresa Sanz-Martínez, Janire Perurena-Prieto, Alfredo Guillén-Del-Castillo, Chiara Bellocchi, Lorenzo Beretta, Eduardo L. Callejas-Moraga, Carmen Pilar Simeón-Aznar
Publikováno v:
Rheumatology (Oxford, England). 61(1)
Objective To analyse the prevalence, the clinical characteristics, the overall survival and the event-free survival (EFS) of SSc patients who express anti-U11/U12 RNP (RNPC-3) antibodies. Methods A total of 447 SSc patients from Barcelona (n = 286) a
Autor:
A. Gil-Vila, M. Roca-Herrera, Alfredo Guillén-Del-Castillo, Albert Selva-O'Callaghan, J. Perurena-Prieto, C. Codina, V. Fonollosa-Pla, C. P. Simeón-Aznar, I. Sanz-Pérez, Eduardo L. Callejas-Moraga
Publikováno v:
Annals of the Rheumatic Diseases. 80:442.1-442
Background:Gastric antral vascular ectasia (GAVE) is one of the gastrointestinal (GI) manifestations related to systemic sclerosis (SSc). It can be presented as iron deficiency anemia or even upper gastrointestinal bleeding. GAVE is diagnosed by endo
Autor:
Ana Marín-Sánchez, Jaime García de Tena, Eduardo L. Callejas-Moraga, Vicent Fonollosa-Pla, Carmen Pilar Simeón-Aznar, Alfredo Guillén-del Castillo, Albert Selva-O'Callaghan, David Bernal-Bello
Publikováno v:
Autoimmunity Reviews. 16:461-468
Emerging data have shown an increased risk of malignancy among patients diagnosed with systemic sclerosis (SSc) so identification of risk factors linking both disorders might have prognostic implications. The aim of this study was to assess the clini
Autor:
Carina Espinet, Alfredo Guillén-del Castillo, Albert Roque, Santiago Aguade, Eduardo L. Callejas-Moraga, Carmen Pilar Simeón-Aznar, Victor Pineda, María Nazarena Pizzi, Isidro Sanz, Maria Roca
Publikováno v:
Saturday, 15 June 2019.
Background: Systemic sclerosis (SSc) is a systemic disease that may affect many organs; among them, cardiac involvement. The prevalence of cardiac involvement in SSc varies depending on the sensitivity of the methods used for its detection. Indirect
Autor:
Eduardo L. Callejas-Moraga, Alfredo Guillén-del Castillo, Carmen Pilar Simeón-Aznar, Isidro Sanz Pérez, Fernando Martínez-Valle, Olimpia Orozco-Gálvez, Vicent Fonollosa-Pla
Publikováno v:
Scleroderma, myositis and related syndromes.
Background Carotid Doppler-ultrasound is useful for the detection of subclinical atheromatosis(1), and also for the evaluation of hemodynamic characteristics of carotid arteries(2). Objectives The aim of this study is to evaluate the hemodynamic para
Autor:
Mónica Rodríguez Carballeira, C Tolosa, Vicent Fonollosa-Pla, Xavier Pla Salas, Isabel Perales Fraile, Eduardo L. Callejas-Moraga, Carmen Pilar Simeón-Aznar, José Antonio Todolí Parra, Alfredo Guillén-del Castillo, Luis Trapiella Martínez, Adela Marín Ballvé
Publikováno v:
Saturday, 15 June 2019.
Background Scleroderma Renal Crisis (SRC) is a serious complication of Systemic Sclerosis (SSc). Nowadays, it seems that there is a reduction in its prevalence and mortality1. Objectives To evaluate the characteristics of patients with SRC in a large
Autor:
Eduardo L. Callejas-Moraga, I. Rodriguez-Pubto, Carmen Pilar Simeón-Aznar, M Freire, I. Pons Martin del Campo, A. Guillén del Castillo, M. E. Sánchez García, Luis Sáez-Comet, J. A. Todolí Parra, José Antonio Vargas-Hitos, V. Fonollosa-Pla, X. Pla Salas, L. Trapiella Martínez, C. Tolosa, J. Sánchez-Redondo
Publikováno v:
Annals of the Rheumatic Diseases. 79:411.1-412
Background:Scleroderma renal crisis (SRC) prevalence is decreasing. However, no Systemic Sclerosis (SSc) patient’s registry has evaluated that decrease over time. No treatment have been able to prevent SRC development.Objectives:Primary objective:
Autor:
I. Sanz Pérez, María Nazarena Pizzi, A. Fernández Codina, Alfredo Guillén-Del-Castillo, V Fonollosa Pla, H. Cuéllar Calabria, A. Roque Pérez, O. Orozco Gálvez, C.P. Simeón Aznar, Eduardo L. Callejas-Moraga, F. Martínez Valle
Publikováno v:
Autoimmunity reviews. 17(9)
Background and objectives Recently published population-based cohort studies have shown a high prevalence of cardiovascular disease in Systemic Sclerosis (SSc) patients. The aim of this study is to compare three different methods to measure cardiovas