Huadong Zhao

Changsha, China

Last Updated: 09/26/2026

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Found 12 publications

Novel VRK1 Variants and a Founder Effect in Axonal Polyneuropathy.

Novel VRK1 Variants and a Founder Effect in Axonal Polyneuropathy.

Journal: Neurology. Genetics

Published: September 20, 2025

Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies.

Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies.

Journal: Journal of the peripheral nervous system : JPNS

Published: February 25, 2025

Genotype-phenotype correlations of AR-CMT2S in a cohort of axonal Charcot-Marie-Tooth patients from Central South China.

Genotype-phenotype correlations of AR-CMT2S in a cohort of axonal Charcot-Marie-Tooth patients from Central South China.

Journal: Journal of the peripheral nervous system : JPNS

Published: April 03, 2024

Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.

Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: March 03, 2024

Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation.

Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation.

Journal: Journal of the peripheral nervous system : JPNS

Published: January 19, 2024

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot-Marie-Tooth Disease.

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot-Marie-Tooth Disease.

Journal: Journal of neurology

Published: June 11, 2023

The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies.

The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies.

Journal: Journal of neurology

Published: May 06, 2023

Expanding the genetic and clinical spectrum of SORD-related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement.

Expanding the genetic and clinical spectrum of SORD-related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement.

Journal: Journal of the peripheral nervous system : JPNS

Published: May 06, 2023

One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families.

One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families.

Journal: Frontiers in neurology

Published: July 05, 2021

Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China.

Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China.

Journal: European journal of neurology

Published: June 07, 2021

Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families.

Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families.

Journal: Frontiers in neurology

Published: September 04, 2020

A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family.

A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family.

Journal: Clinical genetics

Published: April 03, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026