Results 31 to 40 of about 11,147,283 (241)

Discordance Between Patient and Physician Global Assessments in Early Systemic Sclerosis

Arthritis Care &Research, EarlyView.
Objective This study aims to identify factors associated with patient global assessment (PtGA) and physician global assessment (PhGA) and discordance between them in systemic sclerosis (SSc). Methods Data from adults with early SSc (<5 years) from the Collaborative National Quality and Efficacy Registry were included.
Ellen Romich, Alexis Ogdie, Alisa Stephens Shields, Peter A. Merkel, Shervin Assassi, Elana J. Bernstein, Andreea Bujor, Flavia V. Castelino, Lorinda Chung, Luke B. Evnin, Tracy M. Frech, Jessica K. Gordon, Melissa Griffith, Faye N. Hant, Monica L. Harding, Laura K. Hummers, Dinesh Khanna, Kimberly S. Lakin, Dorota J. Lebiedz‐Odrobina, Yiming Luo, Ashima Makol, Maureen D. Mayes, Zsuzsanna H. McMahan, Jerry Molitor, Duncan F. Moore, Julie Paik, Carrie Richardson, Brian Skaug, Ami A. Shah, Ankoor Shah, Virginia Steen, John M. VanBuren, Elizabeth R. Volkmann, Carleigh Zahn, Nora Sandorfi, for the CONQUER Investigators   +35 more
wiley   +1 more source

Research progress on the role of T helper cells 17 and interleukin 17 in oral mucosal diseases

口腔疾病防治, 2021
T helper 17 (Th17) cells are a new type of CD4+ T helper cell. They participate in the immune and inflammatory response by secreting specific interleukin-17 (IL-17).
WANG Ziying, CHEN Xiaotao
doaj   +1 more source

Behçet's disease: review with emphasis on dermatological aspects

Anais Brasileiros de Dermatologia, 2017
Behçet's disease is a systemic vasculitis characterized by attacks of acute inflammation, which can affect almost every vascularized area of the body. There is a close correlation between the geographical distribution of HLA-B51 and its prevalence.
M. Scherrer, V. B. Rocha, Lucas Campos Garcia   +2 more
semanticscholar   +1 more source

Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behcet's Disease

, 2021
Objective Behcet's disease is a complex systemic inflammatory vasculitis of incompletely understood etiology. This study was undertaken to investigate genetic associations with Behcet's disease in a diverse multiethnic population.
DİRESKENELİ, RAFİ HANER, ALİBAZ ÖNER, FATMA   +1 more
core   +1 more source

Treatment of a Large Cohort of Childhood Chronic Noninfectious Uveitis in a Multicentric Large Study: Adalimumab Versus Methotrexate as First‐Line Therapy

Arthritis &Rheumatology, EarlyView.
Objective Treatment of childhood chronic idiopathic uveitis (cCIU) is predominantly based on studies in juvenile idiopathic arthritis–associated uveitis and expert opinion. Our aim was to report the treatment outcomes of our cohort of cCIU. Methods Retrospective multicenter study involving the rheumatology and ophthalmology units at Florence, Italy ...
Ilaria Maccora, Catherine Guly, Cinzia de Libero, Giulia Carreras, Athimalaipet V. Ramanan, Gabriele Simonini   +5 more
wiley   +1 more source

The Evaluation of Coagulation Parameters and Vessel Involvement in Behcet’ s Disease. A Clinical Experience of Behcet’ s Disease: Study of 152 Cases

Acta Medica Iranica, 2013
Behcet´s disease (BD) is accepted as a systemic vasculitis. Vasculitis is observed  predominantly on the venous system. Vessel involvement is frequently seen in males.
Ece Harman, Mehmet Sayarlıoglu, Mustafa Harman, Hayriye Sayarlıoglu   +3 more
doaj   +2 more sources

Surgical lung biopsy to diagnose Behcet′s vasculitis with adult respiratory distress syndrome

Lung India, 2014
A 34-year-old female presented with fever and abdominal pain. Past medical history includes Crohn′s and Behcet′s disease. Examination revealed multiple skin ulcerations, oral aphthae, and bilateral coarse rales.
Ravikanth Vydyula, Charles Allred, Mariana Huartado, Bushra Mina   +3 more
doaj   +1 more source

Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet’s disease susceptibility

Nature Genetics, 2017
We analyzed 1,900 Turkish Behçet's disease cases and 1,779 controls genotyped with the Immunochip. The most significantly associated SNP was rs1050502, a tag SNP for HLA-B*51.
M. Takeuchi, N. Mizuki, A. Meguro, M. Ombrello, Y. Kirino, Colleen L. Satorius, J. Le, M. Blake, B. Erer, T. Kawagoe, D. Ustek, İ. Tuğal-Tutkun, E. Seyahi, Y. Ozyazgan, I. Sousa, F. Davatchi, V. Francisco, F. Shahram, B. Abdollahi, A. Nadji, Niloofar Mojarad Shafiee, Fahmida Ghaderibarmi, S. Ohno, A. Ueda, Y. Ishigatsubo, M. Gadina, S. A. Oliveira, A. Gül, D. Kastner, E. Remmers   +29 more
semanticscholar   +1 more source

A Multifaceted Interplay Among Hemophagocytosis, Interleukin‐18, and Type I Interferon Distinguishes Still Disease From Other Autoinflammatory Diseases

Arthritis &Rheumatology, EarlyView.
Objective The unknown pathophysiology and the lack of specific features for systemic juvenile idiopathic arthritis and adult‐onset Still disease (collectively known as Still disease; SD) delay diagnosis and appropriate treatment. The goal of this study was to identify features and mechanisms that distinguish SD from other systemic autoinflammatory ...
Yvonne M. Mueller, Charlotte Girard, Harmen J. G. van de Werken, Stefan J. Erkeland, Dwin G. B. Grashof, Laurie Vaillant, Renske J. H. den Dekker, Iris van Zuijen, Sharon Veenbergen, Fanny Coffin, Eric Bindels, Yvan Jamilloux, Katerina Laskari, Vassili Soumelis, Bruno Fautrel, Cem Gabay, Peter D. Katsikis   +16 more
wiley   +1 more source

Effects of COVID-19 Pandemic on Psychological Condition and Disease Severity in Patients with Behcet’s Disease

Psychiatry and Behavioral Sciences, 2020
Objectives: Behcet's disease (BD) is an episodic and chronic multisystemic disease. Many comorbid psychiatric disorders are frequently encountered in BD.
Adem Kucuk, Hulya Vatansev, Sakir Gica, Salih Demir, Erkan Cure   +4 more
doaj   +1 more source