Kidney Disorder | List of Frontiers open access articles

Mini Review

Published on 05 Jul 2023

Research progress on Cornus officinalis and its active compounds in the treatment of diabetic nephropathy

in Ethnopharmacology

Chenguang Wu
Jingjing Wang
Rui Zhang
Hailing Zhao
Xin Li
Lifan Wang
Peng Liu
Ping Li

Frontiers in Pharmacology

doi 10.3389/fphar.2023.1207777

6,460 views
26 citations

Case Report

Published on 18 Dec 2025

Case Report: UMOD gene mutation and phenotypic overlap with REN in autosomal dominant tubulointerstitial kidney disease

in Genetics of Common and Rare Diseases

Jingying Xu
Enhui Chen
Wen Shi
Wenhui He
Dongrong Yu
Xianfa Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1661377

1,444 views

Original Research

Published on 23 Aug 2023

Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane

in Neurogenetics

Hongliang Xu
Hanyu Lv
Xin Chen
Yajun Lian
Guolan Xing
Yingzi Wang
Ruimin Hu

Frontiers in Neurology

doi 10.3389/fneur.2023.1231605

3,757 views
2 citations

Case Report

Published on 02 Aug 2021

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

in Pediatric Nephrology

Yu-Xing Liu
Ai-Qian Zhang
Fang-Mei Luo
Yue Sheng
Chen-Yu Wang
Yi Dong
Liangliang Fan
Lv Liu

Frontiers in Pediatrics

doi 10.3389/fped.2021.687455

4,344 views
6 citations

Original Research

Published on 19 Apr 2023

Sperm morphological abnormalities in autosomal dominant polycystic kidney disease are associated with the Hippo signaling pathway via PC1

in Reproduction

Wei-Hui Shi
Zhi-Yang Zhou
Mu-Jin Ye
Ning-Xin Qin
Zi-Ru Jiang
Xuan-You Zhou
Nai-Xin Xu
Xian-Lin Cao
Song-Chang Chen
He-Feng Huang

Frontiers in Endocrinology

doi 10.3389/fendo.2023.1130536

7,174 views
5 citations

Case Report

Published on 26 Nov 2019

The Hypomorphic Variant p.(Gly624Asp) in COL4A5 as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport Syndrome

in Pediatric Nephrology

Eva Pauline Macheroux
Matthias C. Braunisch
Stephanie Pucci Pegler
Robin Satanovskij
Korbinian M. Riedhammer
Roman Günthner
Oliver Gross
Mato Nagel
Lutz Renders
Julia Hoefele

Frontiers in Pediatrics

doi 10.3389/fped.2019.00485

6,883 views
13 citations

Case Report

Published on 10 Dec 2025

Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant

in Pediatric Nephrology

Tuyen Thi Thanh Nguyen
Quynh Thuy Huong Tran
Huong Thi Thanh Nguyen
Trang Quynh Mai Pham
Doan Tran
Kenji Fukui
Hiroyasu Tsukaguchi

Frontiers in Pediatrics

doi 10.3389/fped.2025.1693036

1,018 views

Original Research

Published on 11 Aug 2021

Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

in Molecular Innate Immunity

Marloes A. H. M. Michels
Nicole C. A. J. van de Kar
Sanne A. W. van Kraaij
Sebastian A. Sarlea
Valentina Gracchi
Flore A. P. T. Engels
Eiske M. Dorresteijn
Johannes van der Deure
Caroline Duineveld
Jack F. M. Wetzels

Frontiers in Immunology

doi 10.3389/fimmu.2021.715704

6,551 views
17 citations

Original Research

Accepted on 27 Jan 2026

Clinical value of luciferase‑based bioluminescence assay in diagnosis of Alport syndrome

in Pediatric Nephrology

Yue Cai
Yingqi Lin
Xinyu Kuang
Lei Sun
Mengying Li
Yujie Hu
Wenyan Huang

Frontiers in Pediatrics

192 views

Case Report

Published on 14 May 2024

Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant

in Clinical Research in Nephrology

Paola Krall
Angélica Rojo
Anita Plaza
Sofia Canals
María Luisa Ceballos
Francisco Cano
José Luis Guerrero

Frontiers in Nephrology

doi 10.3389/fneph.2024.1379061

2,677 views
1 citation

Original Research

Published on 16 May 2024

The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822–10T>C, which has been identified as a causative factor for Alport syndrome

in Genetics of Common and Rare Diseases

Lei Liang
Haotian Wu
Jianrong Zhao

Frontiers in Genetics

doi 10.3389/fgene.2024.1330525

2,130 views

Articles

Research progress on Cornus officinalis and its active compounds in the treatment of diabetic nephropathy

Case Report: UMOD gene mutation and phenotypic overlap with REN in autosomal dominant tubulointerstitial kidney disease

Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

Sperm morphological abnormalities in autosomal dominant polycystic kidney disease are associated with the Hippo signaling pathway via PC1

The Hypomorphic Variant p.(Gly624Asp) in COL4A5 as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport Syndrome

Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant

Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

Clinical value of luciferase‑based bioluminescence assay in diagnosis of Alport syndrome

Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant

The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822–10T>C, which has been identified as a causative factor for Alport syndrome