Di Zhang

Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 15 publications

Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation.

Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation.

Journal: Kidney & blood pressure research

Published: April 08, 2023

A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review.

A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review.

Journal: Molecular medicine reports

Published: March 20, 2023

Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome.

Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome.

Journal: Science bulletin

Published: December 27, 2022

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Journal: Frontiers in pediatrics

Published: June 05, 2022

Apparent mineralocorticoid excess: comprehensive overview of molecular genetics.

Apparent mineralocorticoid excess: comprehensive overview of molecular genetics.

Journal: Journal of translational medicine

Published: April 25, 2022

A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension.

A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension.

Journal: Frontiers in cardiovascular medicine

Published: March 15, 2022

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Journal: Frontiers in pediatrics

Published: March 01, 2022

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension.

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension.

Journal: Frontiers in pediatrics

Published: September 29, 2021

Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia.

Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia.

Journal: Endocrine

Published: May 06, 2020

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia.

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia.

Journal: Frontiers in pediatrics

Published: March 16, 2020

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.

Journal: Kidney & blood pressure research

Published: February 24, 2020

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Journal: American journal of hypertension

Published: February 18, 2020

Showing 1-12 of 15

Last Updated: 09/26/2026