Results 131 to 140 of about 8,337 (255)
Whole-exome sequencing in pediatric patients with glomerulonephritis. [PDF]
Peric M +9 more
europepmc +1 more source
Objective We conducted formative research aimed at identifying solutions that address inequitable health outcomes in lupus due to adverse social determinants of health (SDoH). Methods We conducted a search for keywords, which provided insights into potential solutions and initiatives underway. An advisory panel of lupus experts iteratively reviewed the
Joy Buie +11 more
wiley +1 more source
Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis. [PDF]
Melo MAW +3 more
europepmc +1 more source
Objective This study aimed to identify in patients with systemic lupus erythematosus (SLE) with clinically active disease the attainment of frequency and determinants of Lupus Low Disease Activity State (LLDAS) and Definition of Remission in SLE (DORIS) and the frequency and determinants of flare and damage accrual after target attainment.
Yanjie Hao +39 more
wiley +1 more source
Clinical features of hearing loss and genotype-phenotype correlations in Alport syndrome caused by COL4A4 or COL4A5 variants. [PDF]
Matsuzaki S +10 more
europepmc +1 more source
Objective Systemic lupus erythematosus (SLE) is an autoimmune disease that affects numerous organs. Neutrophil extracellular traps (NETs) contribute to sterile inflammation and autoantibody generation in SLE. Isolevuglandins (isoLGs) are reactive oxygen species that are formed during NETosis and contribute to chromatin expansion.
Jaya Krishnan +7 more
wiley +1 more source
Case report: Surgical and clinical results in bilateral lenticonus due to Alport syndrome. [PDF]
Çakmak-Cengiz E +2 more
europepmc +1 more source
Objective The therapeutic effects of telitacicept combined with standard of care (SoC) in childhood‐onset systemic lupus erythematosus (cSLE) remain unclear. This study aims to evaluate its efficacy in comparison with belimumab combined with SoC.
Chong Luo +15 more
wiley +1 more source
A rare case of dual glomerular pathology: Alport syndrome and immune complex-mediated MPGN. [PDF]
Ozcan SG +6 more
europepmc +1 more source

