Results 71 to 80 of about 15,299 (212)

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

Internal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar, Jun Yen Ng, Adam Bryant, Annmarie Bosco, Hugh C. Caterson, Pratyush Giri, Pravin Hissaria, Simon J. Harrison, Stephen Lade, Connull Leslie, Jacinta Perram, H. Miles Prince, Dejan Radeski, Maureen Rischmueller, Craig Wallington‐Gates, Nicholas Weber, Alberta Hoi   +16 more
wiley   +1 more source

Management of Non‐Plaque‐Induced Gingival Conditions: A Systematic Review—Part 2: Inflammatory and Immune Conditions; Neoplasms; and Gingival Pigmentation

Journal of Clinical Periodontology, EarlyView.
ABSTRACT Aims This systematic review assesses current evidence on the management of non‐plaque (dental biofilm)‐induced gingival diseases and conditions (NPIGDs), including (i) inflammatory and immune conditions, (ii) neoplasms and (iii) gingival pigmentations.
Maria Clotilde Carra, Cecile Wasielewski, Bruno Špiljak, Maja Sabalić‐Schoener, Sebastien Jungo, Ivan Alajbeg   +5 more
wiley   +1 more source

Aquaporin-4 IgG antibody-related disorders in patients with juvenile systemic lupus erythematosus [PDF]

, 2019
Objective The aim of this study was to: (a) screen a large group of unselected patients with juvenile systemic lupus erythematosus for anti-aquaporin 4 antibodies (AQP4-Ab); (b) identify clinical and laboratory predictors of the presence of AQP4-Ab ...
Stathopoulos, Y, Sen, D, Moraitis, E, Mankad, K, Hemingway, C, Eleftheriou, D, Al-Obaidi, M, Hong, Y, Hacohen, Y   +8 more
core  

Renal Disease in ROSAH Syndrome Masquerading as Lupus Nephritis: A Case Report and Cohort Analysis

Kidney Medicine
ROSAH (retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and headache) syndrome is a rare, autosomal dominant autoinflammatory disorder caused by gain-of-function mutations in ALPK1.
Anirban Ganguli, Manisha Uppal, Shigeaki Umeda, David E. Kleiner, Christina Kozycki   +4 more
doaj   +1 more source

Risk of urinary tract infection with SGLT2 inhibitor initiation in patients with immune‐mediated inflammatory diseases and type 2 diabetes: A target trial emulation using a Japanese hospital‐based claims database

Journal of Diabetes Investigation, EarlyView.
In this target trial emulation of patients with immune‐mediated inflammatory diseases and type 2 diabetes, SGLT2 inhibitor initiation was not associated with a clear increase in UTI risk versus metformin, including across immunosuppressive therapy strata.
Hiroshi Tsushima, Nobuyuki Yajima, Takashi Nomiyama, Ryoko Sakai, Hisashi Noma, Akira Katagiri, Naoto Tamura   +6 more
wiley   +1 more source

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

Periodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer, Luigi Nibali, Noha Zoheir, Niki M. Moutsopoulos, Bruno G. Loos   +4 more
wiley   +1 more source

Supplemental Material - Cell activation, PD-1 expression and in vitro cytokine production in patients with juvenile systemic lupus erythematosus

, 2022
Supplemental Material for Cell activation, PD-1 expression and in vitro cytokine production in patients with juvenile systemic lupus erythematosus by Juliana Yamada, Octávio AB Peracchi, Maria T Terreri, and Maria Isabel de Moraes-Pinto in ...
Maria T Terreri (12462262), Maria Isabel de Moraes-Pinto (13117921), Juliana Yamada (9651279), Octávio AB Peracchi (9651273)   +3 more
core   +1 more source

In Vitro Fertilization is Essential Healthcare for Patients With Rheumatic Disease

ACR Open Rheumatology, Volume 8, Issue 7, July 2026.
Infertility presents a profound physical, emotional, and financial burden, particularly for rheumatology patients who often face substantial barriers to family building. The 2024 Alabama Supreme Court ruling in LePage v. Center for Reproductive Medicine equating embryo destruction with wrongful death introduced new legal uncertainties, sparking ...
Amanda Moyer, Catherine A. Sims, Rosalind Ramsey‐Goldman, Solmaz Chamanara, Cuoghi Edens   +4 more
wiley   +1 more source

Juvenile Lupus Erythematosus: Fourteen Years of Experience

, 2011
Objectives: This study aims to describe the main clinical and laboratory features as well as the morbidity and mortality of juvenile systemic lupus erythematosus (JSLE) in Turkish ...
Tulpar, Sebahat, Poyrazoglu, Hakan, DÜŞÜNSEL, Ruhan, Gunduz, Zübeyde, Bastug, Funda   +4 more
core   +1 more source

Macrophage Activation Syndrome: A Report of Two Cases and a Literature Review

Case Reports in Rheumatology, 2017
Macrophage activation syndrome (MAS) is a severe, potentially fatal condition that may complicate autoimmune diseases, and it belongs to hemophagocytic lymphohistiocytosis (HLH) disorders. MAS occurs in adults and children.
Asaad Alkoht, Ibrahem Hanafi, Basheer Khalil   +2 more
doaj   +1 more source