Results 31 to 40 of about 81,432 (269)

Ocular sarcoidosis in adults and children: update on clinical manifestation and diagnosis

Journal of Ophthalmic Inflammation and Infection, 2023
Sarcoidosis-associated uveitis, is the predominant ocular sarcoidosis presentation, which affects both adults and children. For adults, international ocular sarcoidosis criteria (IWOS) and sarcoidosis-associated uveitis criteria (SUN) are defined ...
Magdalena Bazewicz, Jarmila Heissigerova, Carlos Pavesio, François Willermain, Janusz Skrzypecki   +4 more
doaj   +1 more source

Characteristics and clinical outcomes of patients with Sarcoidosis admitted for ST-elevation myocardial infarction in the United States: A propensity matched analysis from the National Inpatient Sample

Archives of Medical Science: Atherosclerotic Diseases
Introduction Sarcoidosis is a systemic inflammatory disorder characterised by non-caseating granulomas. Cardiac sarcoidosis (CS) normally causes conduction abnormalities, ventricular arrhythmias, and heart failure.
Raheel Ahmed, Noem Najam, Kamleshun Ramphul, Sebastian Mactaggart, Mansimran Singh Dulay, Joseph Okafor, Alessia Azzu, Maham Bilal, Rahat A Memon, Hemamalini Sakthivel, Rajdeep Khattar, Athol Umfrey Wells, John Arun Baksi, Kshama Wechalekar, Vasilis Kouranos, Anwar Chahal, Rakesh Sharma   +16 more
doaj   +1 more source

Granulomatous Sarcoidosis Mimics

Frontiers in Medicine, 2021
Many granulomatous diseases can mimic sarcoidosis histologically and in terms of their clinical features. These mimics include infectious granulomatous diseases, granulomatous reactions to occupational and environmental exposures, granulomatous drug ...
Marc A. Judson
doaj   +1 more source

[Sarcoidosis]. [PDF]

Pathologica, 1996
SummarySarcoidosis is a multisystem granulomatous disorder of unknown aetiology. The condition commonly affects young adults and frequently presents with bilateral hilar lymphadenopathy with or without pulmonary infiltration, ocular or cutaneous lesions. The clinical presentation can be extremely varied depending upon the organs affected. The diagnosis
CHILOSI, Marco, MENESTRINA, Fabio
openaire   +5 more sources

Coeliac disease and risk of sarcoidosis

, 2007
BACKGROUND AND AIM: Several case reports indicate a link between coeliac disease (CD) and sarcoidosis. Our main objective was to investigate the risk of subsequent sarcoidosis in individuals with CD in a general population cohort study.
Wahlstrom, Jan, Ekbom, Anders, Ludvigsson, Jonas F., Montgomery, Scott M.,, Grunewald, Johan   +4 more
core   +1 more source

Sarcoidosis

The Lancet, 2003
There have been several new insights into the cause and treatment of sarcoidosis. Studies of genetic variation have shown that specific genetic polymorphisms are associated with increased risk of disease or affect disease presentation. These polymorphisms include variation of MHC and cytokines such as tumour necrosis factor (TNF). Not all investigators
Robert P, Baughman, Elyse E, Lower, Roland M, du Bois   +2 more
openaire   +5 more sources

Cutaneous Sarcoidosis- A Report of Two Intriguing Cases [PDF]

Journal of Clinical and Diagnostic Research, 2020
Sarcoidosis is an inflammatory disease which leads to formation of noncaseating granuloma in the affected organs like lungs, lymph nodes and less commonly the skin.
R Mathumathy, S Murugan, S Adikrishnan, R Sivayogana   +3 more
doaj   +1 more source

Athrogenic Indices Can Predict Atherosclerosis in Patients with Sarcoidosis

, 2022
Background: Sarcoidosis is a multisystemic disease of unknown etiology characterized by non-caseating granulomatous inflammation. In this study, we aimed to investigate the efficiency of atherogenic indices and ultrasonographic evaluation of carotid ...
Selendili, Okan, Günay, Sibel, Çilekar, Şule, Kaçar, Emre, Günay, Ersin, Öz, Gürhan, Dumanlı, Ahmet   +6 more
core   +1 more source

Nationwide and international registries on scleroderma. Past, present, and future

Spanish Journal of Medicine, 2021
Systemic sclerosis (SSc) is a low-incidence autoimmune disease that requires collaborative work through national or international registries to advance scientifically.
Manuel Rubio-Rivas
doaj   +1 more source

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio‐based Whole‐Exome Sequencing

Advanced Science, EarlyView.
A rare de novo IFT122‐A773E variant is identified in idiopathic pediatric uveitis and shown to exacerbate retinal inflammation and barrier dysfunction. Mechanistically, the variant enhances IFT43 interaction, elevates calcium signaling, and activates the MEK/ERK/FRA1 axis, revealing a previously unrecognized cilia‐associated pathway that may increase ...
Qian Zhou, Jiaxing Huang, Yilin Wang, Xingran Li, Xianyang Liu, Lingyu Dai, Hongshun Li, Qingfeng Wang, Jiangyi Liu, Guannan Su, Wanyun Zhang, Yang Deng, Qingfeng Cao, Yujie Lai, Xiang Luo, Changwei Huang, Ling Chen, Shengping Hou, Peizeng Yang   +18 more
wiley   +1 more source