Results 21 to 30 of about 216,693 (188)

C3 glomerulopathy disease

open access: yesCumhuriyet Medical Journal, 2018
C3 glomerulopati (C3G), kompleman aktivasyonunun anormal kontrolü ile oluşan bir grup böbrek hastalığını kapsayan yakın zamanda tanımlanmış bir hastalıktır.
Ferhan Candan³   +2 more
core   +4 more sources

C3 Glomerulopathy and related disorders in children [PDF]

open access: yes, 2021
Background and objectives: Membranoproliferative Glomerulonephritis (MPGN) and C3 Glomerulopathy are rare and overlapping disorders associated with dysregulation of the alternative complement pathway.
Gale, Daniel P.   +56 more
core   +2 more sources

C3 glomerulopathy

open access: yesCleveland Clinic Journal of Medicine, 2023
C3 glomerulopathy (C3G) is a rare kidney disease that causes kidney dysfunction as a result of dysregulation of the complement system alternate pathway (AP). C3G encompasses 2 separate disorders, C3 glomerulonephritis and dense deposit disease. The presentation and natural history is variable and kidney biopsy is needed to confirm the diagnosis.
Ali, Mehdi, Jonathan J, Taliercio
openaire   +2 more sources

Clinical Images: Anti-MDA5 dermatomyositis with rapidly progressive interstitial lung disease presenting with rapidly progressive glomerulonephritis due to C3 glomerulopathy. [PDF]

open access: yesACR Open Rheumatol
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Lebhar J   +6 more
europepmc   +2 more sources

Characterization of C3 in C3 glomerulopathy [PDF]

open access: yesNephrology Dialysis Transplantation, 2016
Abstract Background: C3 glomerulopathy (C3G) is caused by overactivity of the alternative pathway of complement that results in bright glomerular C3 staining with minimal or no deposition of immunoglobulins on immunofluorescence microscopy.
Sanjeev, Sethi   +7 more
openaire   +2 more sources

Overview of C3 Glomerulopathy [PDF]

open access: yesFrontiers in Pediatrics, 2016
C3 glomerulopathy is an umbrella term, which includes several rare forms of glomerulonephritis (GN) with underlying defects in the alternate complement cascade. A common histological feature noted in all these GN is dominant C3 deposition in the glomerulus.
Master Sankar Raj, Vimal   +2 more
openaire   +2 more sources

Recurrence of rare disease after kidney transplant [PDF]

open access: yesJournal of Nephropharmacology, 2023
The incidence of chronic kidney diseases (CKDs) by rare etiologies is growing along with other CKDs. This mini-review discusses the epidemiology, pathogenesis, clinical presentation, and diagnosis of rare kidney disease recurrence after kidney ...
Farahnoosh Farnood   +4 more
doaj   +1 more source

C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes [PDF]

open access: yes, 2021
BACKGROUND AND OBJECTIVES: Membranoproliferative GN and C3 glomerulopathy are rare and overlapping disorders associated with dysregulation of the alternative complement pathway.
Wilson, V   +24 more
core   +1 more source

C3 Glomerulopathy and Related Disorders in Children. [PDF]

open access: yes
Background and objectives: Membranoproliferative Glomerulonephritis (MPGN) and C3 Glomerulopathy are rare and overlapping disorders associated with dysregulation of the alternative complement pathway.
Morgan BP   +23 more
core   +4 more sources

C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction

open access: yesCase Reports in Nephrology and Dialysis, 2018
The advances in our understanding of the alternative pathway have emphasized that uncontrolled hyperactivity of this pathway causes 2 distinct disorders that adversely impact the kidney.
Ravneet Bajwa   +10 more
doaj   +1 more source

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