نتایج جستجو برای: diffuse cutaneous scleroderma

تعداد نتایج: 124685  

2011
Matthew R McCann Roxana Monemdjou Parisa Ghassemi-Kakroodi Hassan Fahmi Gemma Perez Shangxi Liu Xu Shi-wen Sunil K Parapuram Fumiaki Kojima Christopher P Denton David J Abraham Johanne Martel-Pelletier Leslie J Crofford Andrew Leask Mohit Kapoor

INTRODUCTION Microsomal prostaglandin E2 synthase-1 (mPGES-1) is an inducible enzyme that acts downstream of cyclooxygenase (COX) to specifically catalyze the conversion of prostaglandin (PG) H2 to PGE2. mPGES-1 plays a key role in inflammation, pain and arthritis; however, the role of mPGES-1 in fibrogenesis is largely unknown. Herein, we examine the role of mPGES-1 in a mouse model of skin sc...

2005
Adil I. Khan

labmedicine.com November 2005 Volume 36 Number 11 LABMEDICINE 723 Systemic sclerosis is a chronic disease of unknown etiology characterized by abnormal accumulation of fibrous tissue in the skin and multiple organs.1 Scleroderma derives its name from the Greek words “sclerosis” (hardness) and “derma” (skin), thus aptly named “hard skin,” a feature that is common to all the different types of sc...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Michael L Whitfield Deborah R Finlay John Isaac Murray Olga G Troyanskaya Jen-Tsan Chi Alexander Pergamenschikov Timothy H McCalmont Patrick O Brown David Botstein M Kari Connolly

We used DNA microarrays representing >12,000 human genes to characterize gene expression patterns in skin biopsies from individuals with a diagnosis of systemic sclerosis with diffuse scleroderma. We found consistent differences in the patterns of gene expression between skin biopsies from individuals with scleroderma and those from normal, unaffected individuals. The biopsies from affected ind...

Journal: :Frontiers in Immunology 2023

Scleroderma-like cutaneous lesions have been found in many pathological conditions and they the clinical appearance of sclerotic or scleroatrophic lesions. Affected skin biopsies described histopathological changes similar to those scleroderma located strictly on systemic sclerosis. These can be inflammatory diseases with autoimmune substrate (generalized morphea, chronic graft versus host dise...

Journal: :Annals of the rheumatic diseases 1985
R M Bernstein R S Pereira A J Holden C M Black A Howard B M Ansell

The clinical presentation of scleroderma in childhood is even more varied than in adult life. This study of 19 children shows that antinuclear antibodies (ANA) detected on the HEp2 cell substrate are just as common as in the adult disorders. All seven children with diffuse scleroderma or acrosclerosis were ANA positive, as were eight of the 12 with more localised disease. Antinucleolar antibodi...

Journal: :British Journal of Dermatology 1990

2017
Christine Arango Clara Malagón María del Pilar Gómez Catalina Mosquera Ricardo Yépez Tatiana González Camilo Vargas

Introduction: Juvenile localized scleroderma is a polymorphic disease. It is more prevalent in girls and has a significant morbidity. Extra-cutaneous involvement is common, and polyautoimmunity can reach 7%. The clinical characteristics of this disease in Colombian patients are currently unknown. Objective: To describe the clinical characteristics, morbidity and outcomes in patients with juveni...

Journal: :Annals of the Rheumatic Diseases 2021

Background: Interstitial lung disease (ILD) is the leading cause of death in scleroderma (SSc) with decline FVC as a predictor mortality patients SSc-ILD, especially early course disease. Objectives: The aim this study to determine survival rate SSc-ILD Malaysian cohort from University Malaya Medical Centre (UMMC). Methods: 61 clinically diagnosed were identified and prospectively recruited. Ba...

2014
Vandana Pradhan Anjali Rajadhyaksha Milind Nadkar Pallavi Pandit Prathamesh Surve Maxime Lecerf Jagadeesh Bayry Srinivas Kaveri Kanjaksha Ghosh

Background. Systemic sclerosis (SSc, scleroderma) is a disorder characterized by fibrosis of skin and visceral organs. Pathogenesis of scleroderma is complex and is incompletely understood as yet. Autoantibodies in SSc represent a serologic hallmark which have clinical relevance, with diagnostic and prognostic potential. Objectives. To study distribution of clinical manifestations and to identi...

Journal: :Clinical and experimental rheumatology 2017
Nerea Iniesta Arandia Carmen Pilar Simeón-Aznar Alfredo Guillén Del Castillo Dolores Colunga Argüelles Manuel Rubio-Rivas Luis Trapiella Martínez Francisco José García Hernández Luis Sáez Comet María Victoria Egurbide Arberas Norberto Ortego-Centeno Mayka Freire Begoña Marí Alfonso José Antonio Vargas Hitos Juan José Ríos Blanco José Antonio Todolí Parra Monica Rodríguez-Carballeira Adela Marín Ballvé Antonio Javier Chamorro Fernández Xavier Pla Salas Ana Belen Madroñero Vuelta Manuel Ruiz Muñoz Vicent Fonollosa Pla Gerard Espinosa

OBJECTIVES To assess the clinical manifestations and prognosis of Spanish patients with systemic sclerosis (SSc) according to their immunological profile. METHODS From the Spanish Scleroderma Study Group or RESCLE (Registro de ESCLErodermia as Spanish nomenclature) Registry we selected those patients in which anti-centromere (ACA), anti-topoisomerase I (ATA), and anti-RNA polymerase III (ARA)...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید