KDIGO clinical practice guideline on the evaluation and management of candidates for kidney transplantation
SJ Chadban, C Ahn, DA Axelrod, BJ Foster… - …, 2020 - journals.lww.com
Abstract The 2020 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice
Guideline on the Evaluation and Management of Candidates for Kidney Transplantation is …
Guideline on the Evaluation and Management of Candidates for Kidney Transplantation is …
[HTML][HTML] Association of primary kidney disease type and donor relatedness with live donor kidney transplant outcomes: An analysis of ANZDATA
Rationale & Objective There is limited information about the association between primary
kidney disease and donor relatedness with transplant outcomes. This study addresses this …
kidney disease and donor relatedness with transplant outcomes. This study addresses this …
Renal, auricular, and ocular outcomes of Alport syndrome and their current management
Y Zhang, J Ding - Pediatric Nephrology, 2018 - Springer
Alport syndrome is a hereditary glomerular basement membrane disease caused by
mutations in the COL4A3/4/5 genes encoding the type IV collagen alpha 3–5 chains. Most …
mutations in the COL4A3/4/5 genes encoding the type IV collagen alpha 3–5 chains. Most …
Uncovering modifier genes of X-linked Alport syndrome using a novel multiparent mouse model
Y Takemon, V Wright, B Davenport… - Journal of the …, 2021 - journals.lww.com
Background Mutations in COL4A5 are responsible for 80% of cases of X-linked Alport
Syndrome (XLAS). Although genes that cause AS are well characterized, people with AS …
Syndrome (XLAS). Although genes that cause AS are well characterized, people with AS …
A case report and literature study on Alport syndrome featuring nephrotic syndrome as its primary manifestation
Z Deng, Q Zhou, TG Zhou - Transplant Immunology, 2023 - Elsevier
Background Historically, due to the lack of distinct clinical symptoms, Alport syndrome, a
hereditary kidney disease prevalent in children and a leading cause of kidney failure, has …
hereditary kidney disease prevalent in children and a leading cause of kidney failure, has …
[PDF][PDF] Alport 综合征的临床表现及诊疗进展
赵颖玲, 于力 - JOURNAL OF RARE AND UNCOMMON …, 2022 - diagnoschina.com
Alport 综合征(AS) 是我国常见的具有遗传异质性的儿童肾脏疾病, 以血尿, 听力损坏,
眼部病变及进行性肾功能衰竭等为临床特点, 又被称为家族性出血性肾炎, 遗传性进行性肾炎 …
眼部病变及进行性肾功能衰竭等为临床特点, 又被称为家族性出血性肾炎, 遗传性进行性肾炎 …
Explaining Alport syndrome—lessons from the adult nephrology clinic
H Mabillard, R Ryan, N Tzoumas, S Gear… - Journal of Rare …, 2024 - Springer
Alport syndrome is a genetic kidney disease that causes worsening of kidney function over
time, often progressing to kidney failure. Some types of Alport syndrome cause other …
time, often progressing to kidney failure. Some types of Alport syndrome cause other …
A comprehensive review on inherited Sensorineural Hearing Loss and their syndromes
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world
population effects with different kind of congenital hearing loss (HL). In third-world countries …
population effects with different kind of congenital hearing loss (HL). In third-world countries …
Hereditary Nephritis in Children
J Savige - Evidence‐Based Nephrology, 2022 - Wiley Online Library
Hereditary nephritis usually refers to Alport syndrome and thin basement membrane
nephropathy. Hematuria occurs in about 6% of the pediatric population and is mainly …
nephropathy. Hematuria occurs in about 6% of the pediatric population and is mainly …
[HTML][HTML] Mother–Son Kidney Transplantation in Patients With X-Linked Alport Syndrome
K Katayama, K Nishikawa, A Hane, M Fujimoto… - Kidney International …, 2021 - Elsevier
Alport syndrome (AS) is a hereditary disease that is characterized by progressive kidney
disease, sensorineural hearing loss, and ocular lesions. 1 The responsible genes for AS are …
disease, sensorineural hearing loss, and ocular lesions. 1 The responsible genes for AS are …