[HTML][HTML] IgA nephropathy
JC Rodrigues, M Haas, HN Reich - Clinical Journal of the …, 2017 - journals.lww.com
IgA nephropathy (IgAN) is a leading cause of CKD and renal failure. Recent international
collaborative efforts have led to important discoveries that have improved our understanding …
collaborative efforts have led to important discoveries that have improved our understanding …
[图书][B] Campbell Walsh Wein Urology, E-Book: 3-Volume Set
AW Partin, RR Dmochowski, LR Kavoussi, CA Peters… - 2020 - books.google.com
From the basic science underpinnings to the most recent developments in medical and
surgical care, Campbell-Walsh-Wein Urology offers a depth and breadth of coverage you …
surgical care, Campbell-Walsh-Wein Urology offers a depth and breadth of coverage you …
[HTML][HTML] New insights in the pathogenesis of immunoglobulin A vasculitis (Henoch-Schönlein purpura)
MH Heineke, AV Ballering, A Jamin, SB Mkaddem… - Autoimmunity …, 2017 - Elsevier
Immunoglobulin A vasculitis (IgAV), also referred to as Henoch-Schönlein purpura, is the
most common form of childhood vasculitis. The pathogenesis of IgAV is still largely …
most common form of childhood vasculitis. The pathogenesis of IgAV is still largely …
[HTML][HTML] IgA vasculitis update: epidemiology, pathogenesis, and biomarkers
L Xu, Y Li, X Wu - Frontiers in Immunology, 2022 - frontiersin.org
Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the
most common systemic vasculitis in children, characterized by diverse clinical …
most common systemic vasculitis in children, characterized by diverse clinical …
IgA nephropathy
Abstract Globally, IgA nephropathy (IgAN) is the most common primary glomerulonephritis
that can progress to renal failure. The exact pathogenesis of IgAN is not well defined, but …
that can progress to renal failure. The exact pathogenesis of IgAN is not well defined, but …
[HTML][HTML] Pathogenesis of IgA vasculitis: an up-to-date review
Y Song, X Huang, G Yu, J Qiao, J Cheng, J Wu… - Frontiers in …, 2021 - frontiersin.org
Immunoglobin A (IgA) vasculitis (IgAV), formerly called the Henoch-Schönlein purpura
(HSP), is a small vessel vasculitis, characterized by IgA1-dominant immune deposition at …
(HSP), is a small vessel vasculitis, characterized by IgA1-dominant immune deposition at …
[HTML][HTML] Childhood IgA vasculitis (Henoch Schonlein purpura)—advances and knowledge gaps
L Oni, S Sampath - Frontiers in pediatrics, 2019 - frontiersin.org
Immunoglobulin A vasculitis (IgAV; formerly Henoch Schonlein Purpura) is the most
common form of childhood vasculitis. It can occur in any age and peaks around 4–6 years …
common form of childhood vasculitis. It can occur in any age and peaks around 4–6 years …
[HTML][HTML] New developments in the genetics, pathogenesis, and therapy of IgA nephropathy
R Magistroni, VD D'Agati, GB Appel, K Kiryluk - Kidney international, 2015 - Elsevier
Recent years have brought notable progress in the field of IgA nephropathy. Here, we
highlight important new directions and latest developments, including successful discovery …
highlight important new directions and latest developments, including successful discovery …
[HTML][HTML] Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis
K Kiryluk, Y Li, S Sanna-Cherchi… - PLoS …, 2012 - journals.plos.org
IgA nephropathy (IgAN), major cause of kidney failure worldwide, is common in Asians,
moderately prevalent in Europeans, and rare in Africans. It is not known if these differences …
moderately prevalent in Europeans, and rare in Africans. It is not known if these differences …