Xin-hua Wan

Beijing, 100730, China

Last Updated: 09/26/2026

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Found 15 publications

Clinical and Genetic Spectrum of ANO3-Related Dystonia with Treatment Responses in a Chinese Cohort.

Clinical and Genetic Spectrum of ANO3-Related Dystonia with Treatment Responses in a Chinese Cohort.

Journal: Genes

Published: April 26, 2026

Dystonia-like behaviors and impaired sensory-motor integration following neurotoxic lesion of the pedunculopontine tegmental nucleus in mice.

Dystonia-like behaviors and impaired sensory-motor integration following neurotoxic lesion of the pedunculopontine tegmental nucleus in mice.

Journal: Frontiers in neurology

Published: November 24, 2022

Identification of TH Variants in Chinese Dopa-Responsive Dystonia Patients and Long-Term Outcomes.

Identification of TH Variants in Chinese Dopa-Responsive Dystonia Patients and Long-Term Outcomes.

Journal: Frontiers in neurology

Published: December 22, 2020

Mutations in the VPS16 Gene in 56 Early-Onset Dystonia Patients.

Mutations in the VPS16 Gene in 56 Early-Onset Dystonia Patients.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 07, 2020

A compound heterozygous ALPL variant in a patient with dystonia-parkinsonism and hypointensity in basal ganglia: A case report.

A compound heterozygous ALPL variant in a patient with dystonia-parkinsonism and hypointensity in basal ganglia: A case report.

Journal: Parkinsonism & related disorders

Published: May 15, 2020

Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants.

Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants.

Journal: Parkinsonism & related disorders

Published: February 05, 2020

Progress in the Diagnosis and Management of Chorea-acanthocytosis.

Progress in the Diagnosis and Management of Chorea-acanthocytosis.

Journal: Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih

Published: April 06, 2018

Targeted gene capture sequencing in diagnosis of dystonia patients.

Targeted gene capture sequencing in diagnosis of dystonia patients.

Journal: Journal of the neurological sciences

Published: September 21, 2017

Novel SERAC1 mutations in a Chinese patient presenting with parkinsonism and dystonia.

Novel SERAC1 mutations in a Chinese patient presenting with parkinsonism and dystonia.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: September 02, 2017

Mutations in GNAL gene in 214 cases with isolated dystonia.

Mutations in GNAL gene in 214 cases with isolated dystonia.

Journal: Parkinsonism & related disorders

Published: April 13, 2015

Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families.

Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: November 23, 2014

Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.

Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: January 07, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026