Walter Alberto Sifuentes Giraldo

ORCID: 0000-0003-2548-3988
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About
Contact & Profiles
Research Areas
  • Systemic Sclerosis and Related Diseases
  • Inflammatory Myopathies and Dermatomyositis
  • Systemic Lupus Erythematosus Research
  • Dermatological and Skeletal Disorders
  • Autoimmune and Inflammatory Disorders Research
  • Bone and Joint Diseases
  • Bone health and treatments
  • Immunodeficiency and Autoimmune Disorders
  • Eosinophilic Disorders and Syndromes
  • Lymphoma Diagnosis and Treatment
  • Spondyloarthritis Studies and Treatments
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Monoclonal and Polyclonal Antibodies Research
  • Musculoskeletal synovial abnormalities and treatments
  • Skin Diseases and Diabetes
  • Bone Tumor Diagnosis and Treatments
  • Chronic Lymphocytic Leukemia Research
  • Rheumatoid Arthritis Research and Therapies
  • Sarcoidosis and Beryllium Toxicity Research
  • Peripheral Neuropathies and Disorders
  • Osteomyelitis and Bone Disorders Research
  • Adolescent and Pediatric Healthcare
  • Bone health and osteoporosis research
  • Orthopedic Surgery and Rehabilitation
  • Hematological disorders and diagnostics

Hospital Universitario Ramón y Cajal
2012-2023

Hospital Universitario de Guadalajara
2020-2021

Instituto Ramón y Cajal de Investigación Sanitaria
2019-2020

Center for Rheumatology
2013-2018

Instituto Cajal
2014-2018

Madrid Health Service
2017

National University of Distance Education
2016

Instituto Nacional de Salud del Niño
2016

Marathon Veterinary Hospital
2015

Jabil (United States)
2015

Objectives To determine the causes of death and risk factors in systemic sclerosis (SSc). Methods Between 2000 2011, we examined certificates all French patients with SSc to death. Then developed a score associated all-cause mortality from international European Scleroderma Trials Research (EUSTAR) database. Candidate prognostic were tested by Cox proportional hazards regression model single variable analysis, followed multiple stratified centres. The bootstrapping technique was used for...

10.1136/annrheumdis-2017-211448 article EN Annals of the Rheumatic Diseases 2017-08-23
Lorenzo Cavagna Ernesto Trallero‐Araguás Federica Meloni Ilaria Cavazzana Jorge Rojas‐Serrano and 95 more Eugen Feist Giovanni Zanframundo Valentina Morandi Alain Meyer José António Pereira da Silva Catarina Costa Øyvind Molberg Helena Andersson Veronica Codullo Marta Mosca Simone Barsotti R Neri Carlo Alberto Scirè Marcello Govoni Federica Furini Francisco Javier López-Longo Julia Martínez‐Barrio Udo Schneider Hanns‐Martin Lorenz Andrea Doria Anna Ghirardello Norberto Ortego‐Centeno Marco Confalonieri Paola Tomietto Nicolò Pipitone Ana Rodriguez Cambron María Ángeles Blázquez-Cañamero Reinhard Voll Sarah K. Wendel Salvatore Scarpato F. Maurier Massimiliano Limonta Paolo Luigi Colombelli Margherita Giannini Bernard Gény Eugenio Arrigoni Elena Bravi Paola Migliorini Alessandro Mathieu Matteo Piga Ulrich Drott Christiane Delbrueck Jutta Bauhammer Giovanni Cagnotto Carlo Vancheri Gianluca Sambataro Ellen De Langhe Pier Paolo Sainaghi Maria Cristina Monti Francesca Gigli Berzolari Mariaeva Romano Francesco Bonella Christof Specker Andreas Schwarting Ignacio Villa Blanco Carlo Selmi Angela Ceribelli Laura Nuño Antonio Mera Nair Pérez Gómez Enrico Fusaro Simone Parisi L. Sinigaglia Nicoletta Del Papa Maurizio Benucci Marco A. Cimmino Valeria Riccieri Fabrizio Conti Gian Domenico Sebastiani Anna Iuliano Giacomo Emmi Daniele Cammelli Marco Sebastiani Andreina Manfredi Javier Bachiller‐Corral Walter Alberto Sifuentes Giraldo Giuseppe Paolazzi Lesley Ann Saketkoo Roberto Giorgi Fausto Salaffi José Manuel Cifrián Roberto Caporali Francesco Locatelli Enrico Marchioni Alberto Pesci Giulia Dei Maria Rosa Pozzi Claudia Lomater Jörg H. W. Distler Johannes Knitza George Schett Florenzo Iannone Marco Fornaro Franco Franceschini Luca Quartuccio

Antisynthetase syndrome (ASSD) is a rare clinical condition that characterized by the occurrence of classic triad, encompassing myositis, arthritis, and interstitial lung disease (ILD), along with specific autoantibodies are addressed to different aminoacyl tRNA synthetases (ARS). Until now, it has been unknown whether presence ARS might affect presentation, evolution, outcome ASSD. In this study, we retrospectively recorded time onset, characteristics, clustering triad findings, survival...

10.3390/jcm8112013 article EN Journal of Clinical Medicine 2019-11-18

Anti Jo-1 antibodies are the main markers of antisynthetase syndrome (ASSD), an autoimmune disease clinically characterized by occurrence arthritis, myositis, and interstitial lung (ILD). These manifestations usually co-occur (for practical purpose complete forms) in same patient, but cases with only 1 or 2 these findings incomplete have been described. In forms, ex novo further is possible, although frequencies timing not still defined. The aim this international, multicenter, retrospective...

10.1097/md.0000000000001144 article EN cc-by-nc Medicine 2015-08-01

Adult-onset Still's disease (AOSD) is frequently refractory to standard therapy. Tocilizumab (TCZ) has demonstrated efficacy in single cases and small series of patients with AOSD. The aim this multicenter study was assess the TCZ AOSD conventional treatment.This a retrospective open-label treatment 34 who had experienced an inadequate response corticosteroids at least 1 synthetic immunosuppressive drug also, many cases, biologic agents.The mean ± SD age (8 men 26 women) 38.7 16.1 years....

10.1002/art.38398 article EN Arthritis & Rheumatology 2014-02-11

Adult-onset Still's disease (AOSD) is often refractory to standard therapy. Anakinra (ANK), an interleukin-1 receptor antagonist, has demonstrated efficacy in single cases and small series of AOSD. We assessed the ANK a AOSD patients. Multicenter retrospective open-label study. was used due lack synthetic immunosuppressive drugs some also at least 1 biologic agent. Forty-one patients (26 women/15 men) were recruited. They had mean age 34.4 ± 14 years median [interquartile range (IQR)]...

10.1097/md.0000000000001554 article EN cc-by-nc Medicine 2015-09-01

Objectives: Juvenile systemic sclerosis is a rare childhood disease. Three disease activity indices have been published for adult patients with sclerosis: the European Scleroderma Study Group Index, modified version of Index and revised Trials Research index. The objective this study was to determine feasibility performance three in prospectively followed cohort juvenile sclerosis. Methods: analysis selected from prospective international inception enrolling patients. correlation physicians’...

10.1177/23971983231164700 article EN Journal of Scleroderma and Related Disorders 2023-04-10
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