Xiaoyu Liu

Beijing, China

Last Updated: 09/26/2026

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Found 14 publications

Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy.

Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy.

Journal: Pediatric research

Published: November 23, 2022

Prominent renal complications associated with MMACHC pathogenic variant c.80A > G in Chinese children with cobalamin C deficiency.

Prominent renal complications associated with MMACHC pathogenic variant c.80A > G in Chinese children with cobalamin C deficiency.

Journal: Frontiers in pediatrics

Published: September 29, 2022

Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5.

Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5.

Journal: Frontiers in genetics

Published: April 18, 2021

Value of electron microscopy in the pathological diagnosis of native kidney biopsies in children.

Value of electron microscopy in the pathological diagnosis of native kidney biopsies in children.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 19, 2020

Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.

Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.

Journal: Molecular genetics & genomic medicine

Published: February 01, 2020

Factors predicting the recovery from acute kidney injury in children with primary nephrotic syndrome.

Factors predicting the recovery from acute kidney injury in children with primary nephrotic syndrome.

Journal: Clinical and experimental nephrology

Published: October 14, 2019

Reassessing the pathogenicity of c.2858G>T(p.(G953V)) in COL4A5 Gene: report of 19 Chinese families.

Reassessing the pathogenicity of c.2858G>T(p.(G953V)) in COL4A5 Gene: report of 19 Chinese families.

Journal: European journal of human genetics : EJHG

Published: March 28, 2019

Diverse phenotypes in children with PAX2-related disorder.

Diverse phenotypes in children with PAX2-related disorder.

Journal: Molecular genetics & genomic medicine

Published: December 04, 2018

Steroid-resistant nephrotic syndrome caused by co-inheritance of mutations at NPHS1 and ADCK4 genes in two Chinese siblings.

Steroid-resistant nephrotic syndrome caused by co-inheritance of mutations at NPHS1 and ADCK4 genes in two Chinese siblings.

Journal: Intractable & rare diseases research

Published: December 21, 2017

Diagnosis and treatment of Dent disease in 10 Chinese boys.

Diagnosis and treatment of Dent disease in 10 Chinese boys.

Journal: Intractable & rare diseases research

Published: March 31, 2017

Mutations in TTC21B cause different phenotypes in two childhood cases in China.

Mutations in TTC21B cause different phenotypes in two childhood cases in China.

Journal: Nephrology (Carlton, Vic.)

Published: December 21, 2016

Clinical and genetic features of X-linked Alport syndrome in men positive for the collagen Ⅳ α5 chain in epidermal basement membrane

Clinical and genetic features of X-linked Alport syndrome in men positive for the collagen Ⅳ α5 chain in epidermal basement membrane

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: January 22, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026