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New susceptible locus, rs9428555, is associated with pediatric-onset immunoglobulin A nephropathy and immunoglobulin A vasculitis in Koreans.
Genes Genomics
September 2021
Department of Pediatrics, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon-Si, Gyeonggi-do, Republic of Korea.
Background: Immunoglobulin A nephropathy (IgAN) is one of the most common primary forms of glomerulonephritis, while IgA vasculitis (IgAV) is the most common systemic vasculitis in children.
Objective: Herein we aimed to uncover single nucleotide polymorphism (SNP) markers associated with these two related diseases by applying association tests and Sanger sequencing.
Methods: Within the discovery stage, genomic DNA in blood samples from 101 enrolled patients were genotyped by the Korean Biobank Array.
Introduction to the special issue: "Focus on pediatric nephrology".
J Biol Regul Homeost Agents
November 2019
Chief UOSD Pediatric Nephrology, AOUP Policlinico G. Martino, Messina.
In this special issue, Researchers and Specialist Registrars of University of Catania, Catanzaro and Messina (ITALY) focused on nephron-urological abnormalities in children, ranging from glomerular (nephrosic and Alport syndrome, chronic glomerulonephritis) and urologic diseases (multicystic dysplastic kidney, obstructive pathologies and stones). Particular attention was paid to congenital syndrome, such as Vacterl, Fabry and Goldenhar syndrome and acquired conditions such as Schoenlein-Henoch disease potentially leading to renal impairment. In addition, oxidative stress in newborns is involved in the progression of renal failure.
View Article and Find Full Text PDF[Rapid progressive glomerulonephritis].
Internist (Berl)
May 2019
Medizinische Klinik III - Nieren- und Hochdruckerkrankungen, Klinikum Fulda gAG, Universitätsmedizin Marburg - Campus Fulda, Pacelliallee 4, 36043, Fulda, Deutschland.
The rapid progressive glomerulonephritis is an emergency case. Renal function is rapidly lost within weeks or a few months (rarely within days) due to necrotizing extracapillary proliferative crescentic glomerulonephritis. Early diagnosis and treatment improve prognosis, as the best prognostic marker is creatinine when treatment is initiated.
View Article and Find Full Text PDFThe Spectrum of Biopsy-Proven Glomerular Diseases among Children in China: A National, Cross-Sectional Survey.
Clin J Am Soc Nephrol
July 2018
The National Clinical Research Center for Kidney Disease, State Key Laboratory of Organ Failure Research, Renal Division, Nanfang Hospital and.
Background And Objectives: High-quality epidemiologic data on the spectrum of biopsy-proven glomerular diseases among children are limited. This study aimed to determine the profile of and temporal change in biopsy-proven pediatric glomerular diseases in China.
Design, Setting, Participants, & Measurements: We previously conducted a nationwide kidney biopsy survey including 71,151 patients over an 11-year period from January 2004 to December 2014.
[Henoch-Schönlein purpura in a cocaine consumer man with HIV infection and ANCA-p positivity].
Medicina (B Aires)
February 2017
Centro Sanatorio Delta, Rosario, Santa Fe, Argentina.
The Henoch-Schönlein purpura (HSP) is a small vessel vasculitis with IgA immune complex deposition. The presentation in adults is rare and severe. Reported cases of HSP in patients infected with HIV are scarce.
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