Yanhua Lang

16 Jiangsu Road
Qingdao, 266003, China

Last Updated: 09/26/2026

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Found 24 publications

The influence of two-way referral model on treatment and prognosis of patients with chronic heart failure

The influence of two-way referral model on treatment and prognosis of patients with chronic heart failure

Journal: Zhonghua xin xue guan bing za zhi

Published: November 25, 2025

A novel heterozygous variant of the SALL1 gene with atypical Townes-Brocks syndrome phenotypes in Chinese family.

A novel heterozygous variant of the SALL1 gene with atypical Townes-Brocks syndrome phenotypes in Chinese family.

Journal: Nephrology (Carlton, Vic.)

Published: December 14, 2023

Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay.

Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay.

Journal: Molecular genetics & genomic medicine

Published: September 05, 2023

Four novel variants identified in primary hyperoxaluria and genotypic and phenotypic analysis in 21 Chinese patients.

Four novel variants identified in primary hyperoxaluria and genotypic and phenotypic analysis in 21 Chinese patients.

Journal: Frontiers in genetics

Published: December 15, 2022

Identification of two novel variants of BCS1L gene in a patient with classical GRACILE syndrome.

Identification of two novel variants of BCS1L gene in a patient with classical GRACILE syndrome.

Journal: Nephrology (Carlton, Vic.)

Published: May 23, 2022

Minigene splicing assays reveal new insights into exonic variants of the SLC12A3 gene in Gitelman syndrome.

Minigene splicing assays reveal new insights into exonic variants of the SLC12A3 gene in Gitelman syndrome.

Journal: Molecular genetics & genomic medicine

Published: April 07, 2022

Genotypic and phenotypic analysis in 51 Chinese patients with primary distal renal tubular acidosis.

Genotypic and phenotypic analysis in 51 Chinese patients with primary distal renal tubular acidosis.

Journal: Clinical genetics

Published: March 31, 2021

Identification of seven exonic variants in the SLC4A1, ATP6V1B1, and ATP6V0A4 genes that alter RNA splicing by minigene assay.

Identification of seven exonic variants in the SLC4A1, ATP6V1B1, and ATP6V0A4 genes that alter RNA splicing by minigene assay.

Journal: Human mutation

Published: January 27, 2021

Sudden onset of nephrotic syndrome in an asymptomatic Fabry patient: a case report.

Sudden onset of nephrotic syndrome in an asymptomatic Fabry patient: a case report.

Journal: Renal failure

Published: September 14, 2020

Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2.

Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 03, 2020

Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.

Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.

Journal: Endocrine

Published: August 21, 2019

Eleven novel SLC12A1 variants and an exonic mutation cause exon skipping in Bartter syndrome type I.

Eleven novel SLC12A1 variants and an exonic mutation cause exon skipping in Bartter syndrome type I.

Journal: Endocrine

Published: November 08, 2018

Showing 1-12 of 24

Last Updated: 09/26/2026