Results 81 to 90 of about 1,144,913 (219)

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

Arthritis &Rheumatology, Volume 78, Issue 9, Page 1961-1974, September 2026.
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

Staged Endovascular Intervention for Axillary Artery Aneurysm Complicated by Recurrent Upper Limb Arterial Embolism: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Axillary artery aneurysm is an uncommon subtype of peripheral arterial aneurysm, and mural thrombus within the aneurysm sac frequently dislodges to trigger recurrent refractory acute upper extremity arterial embolism. This study reports a 57‐year‐old male patient who suffered immediate re‐embolization after isolated percutaneous thrombus ...
Xiaolong Li, Yayun Xiao, Yulin Zhang, Liwei Zhang, Qunfeng Liu   +4 more
wiley   +1 more source

Spinal Cord Sarcoidosis Treated With Infliximab

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Isolated spinal cord lesion could be misinterpreted as a demyelinating disease. The diagnosis of sarcoidosis should be in the differential when other indices for a demyelinating disorder are absent. An inadequate response to intravenous steroid therapy should not rule out spinal sarcoidosis as this report confirms the response to intravenous ...
Hussein Moussa, Roula Hourani Rizk, Nina S. Shabb, Nabil El Ayoubi, Raja Sawaya   +4 more
wiley   +1 more source

Behcet syndrome: the vascular cluster

, 2016
Although skin-mucosa lesions are common in almost all patients with Behcet syndrome (BS), clinical properties may differ from one patient to another. Within BS, there are subsets with different organ involvement and hence probably different pathological ...
Seyahi, Emire, Yazici, Hasan
core   +1 more source

When to consider an inborn error of immunity: clues for physicians

Internal Medicine Journal, Volume 56, Issue 9, Page 1488-1499, September 2026.
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley   +1 more source

Mapping the Altered Landscape of TCR Repertoire in Autoimmune Diseases

Immunological Reviews, Volume 342, Issue 1, September 2026.
ABSTRACT Autoimmune diseases arise from the breakdown of immune tolerance through complex interactions between genetic predisposition, environmental exposures, and adaptive immune responses. High‐throughput T‐cell receptor (TCR) repertoire sequencing has transformed our ability to characterize these responses, providing unprecedented insights into ...
Celine Albalaa, Martin Pezous, David Klatzmann, Encarnita Mariotti‐Ferrandiz   +3 more
wiley   +1 more source

CNS involvement in neuro-Behcet syndrome: An MR study

, 1999
BACKGROUND AND PURPOSE: Behcet disease (BD) is a multisystem vasculitis of unknown origin in which neurologic involvement has been reported in the range of 5% to 10% in large series.
Kocer, N, Siva, A, Kantarci, O, Islak, C, Hamuryudan, V, Saip, S, Akman, C   +6 more
core   +1 more source

Recurrent weakness of left limbs for one year

Chinese Journal of Contemporary Neurology and Neurosurgery, 2015
DOI: 10.3969/j.issn.1672-6731.2015.11 ...
Nan LIN, Lin WANG, Hong-jie LI, Li-ying CUI   +3 more
doaj  

Tubulointerstitial Nephritis With Uveitis (TINU) Syndrome: A Case Series and Review of Literature

Nephrology, Volume 31, Issue 9, September 2026.
ABSTRACT Tubulointerstitial nephritis with uveitis (TINU) syndrome is a rare disorder characterised by the simultaneous or sequential occurrence of acute tubulointerstitial nephritis and uveitis, in the absence of systemic disease. Its true prevalence is likely underestimated, as renal and ocular manifestations may not appear concurrently. We conducted
Weaam Ali, Nidhi Agrawal, Smeeta Sinha, Dimitrios Poulikakos, Jamil Choudhury, Constantina Chrysochou   +5 more
wiley   +1 more source

Mesotherapy With Lidocaine and Ketamine in Complex Regional Pain Syndrome Type 1: A Randomized Double‐Blind Trial

Pain Practice, Volume 26, Issue 7, September 2026.
ABSTRACT Background Complex regional pain syndrome type 1 (CRPS1) is a disabling pain syndrome whose treatment remains challenging. Mesotherapy is a therapeutic method involving the injection of low doses of active substances through the skin. No studies assessed mesotherapy in CRPS1 patients.
Philippe Lafuma, Laurent Magaud, Amna Abichou‐Klich, Muriel Rabilloud, Julien Wegrzyn, Christian Baude, Pascal Rippert, Myriam Kaou, Julie Haesebaert, Frédéric Rongieras, Chloé Marchand, Carole Dhelens, Olivia Febvey‐Combes   +12 more
wiley   +1 more source