Immune cells and stromal cells undergo metabolic reprogramming in both rheumatoid and osteoarthritis. This review summarises current evidence on the metabolic changes within and the crosstalk between immune and stromal cells in these diseases. In addition, we explore the therapeutic potential of targeting metabolic processes for the treatment of ...
Órlaith C. Henry, Luke A. J. O'Neill
wiley +1 more source
A Triple Threat: Acute Systemic Lupus Erythematosus Unveiled with Hemophagocytic Lymphohistiocytosis and Toxic Epidermal Necrolysis. [PDF]
Shah C+6 more
europepmc +1 more source
Disparity between Visual Fields and Optical Coherence Tomography in Hydroxychloroquine Retinopathy [PDF]
Michael F. Marmor, Ronald B. Melles
openalex +1 more source
The Efficacy of Platelet‐Rich Plasma in Facial Lichen Planus Pigmentosus: A Prospective Pilot Study
ABSTRACT Background and Aims Lichen planus pigmentosus (LPP) is an uncommon variant of lichen planus which most commonly affects middle‐aged individuals with skin of color. Despite multiple treatment modalities available for LPP, their efficacies are unpredictable and often disappointing.
Chanisa Kiatsurayanon+3 more
wiley +1 more source
Association Between X/Twitter and Prescribing Behavior During the COVID-19 Pandemic: Retrospective Ecological Study. [PDF]
Helgeson SA+7 more
europepmc +1 more source
ABSTRACT Background and Aims Critically ill patients in COVID‐19 to the intensive care unit (ICU) may develop multiple organ dysfunction syndrome, with some requiring extracorporeal organ support. This study aimed to assess the effects of combined CytoSorb hemoperfusion (HP) and continuous renal replacement therapy (CRRT) on the improvement of the ...
Seyed MohammadReza Hashemian+4 more
wiley +1 more source
Case Report: Subacute cutaneous lupus erythematosus induced by the anti-PD-1 antibody camrelizumab combined with chemotherapy. [PDF]
Bao H+11 more
europepmc +1 more source
Systematic Review of Management Strategies for Alport Syndrome: Implications for Male Patients
ABSTRACT Background and Aims Alport Syndrome (AS) is a rare genetic disorder characterized by progressive kidney disease, hearing loss, and ocular abnormalities, with an incidence of approximately 1 in 50,000 newborns. Due to the severity of the disease, particularly in males with X‐linked inheritance, this systematic review consolidates current ...
Zouina Sarfraz+10 more
wiley +1 more source
VEXAS syndrome with p.Met41Leu <i>UBA1</i> gene mutation misdiagnosed as tumid lupus: A series of 3 cases. [PDF]
Mizes A, Ash MM, Richardson CT.
europepmc +1 more source