Yin Ma

88 Jiefang Rd
Hangzhou, 310009, China

Last Updated: 09/26/2026

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Found 15 publications

Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene.

Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene.

Journal: Cerebellum (London, England)

Published: June 04, 2024

Identifying extracerebellar characteristics in a large cohort of 319 Chinese patients with spinocerebellar ataxia type 3.

Identifying extracerebellar characteristics in a large cohort of 319 Chinese patients with spinocerebellar ataxia type 3.

Journal: Chinese medical journal

Published: January 17, 2024

CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1.

CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1.

Journal: Cerebellum (London, England)

Published: July 06, 2023

Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.

Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.

Journal: Translational neurodegeneration

Published: May 31, 2021

Association of the Level of Neurofilament Light With Disease Severity in Patients With Spinocerebellar Ataxia Type 2.

Association of the Level of Neurofilament Light With Disease Severity in Patients With Spinocerebellar Ataxia Type 2.

Journal: Neurology

Published: January 25, 2021

TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study.

TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study.

Journal: Gene

Published: December 10, 2020

Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years.

Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years.

Journal: European journal of neurology

Published: September 18, 2020

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.

Journal: Brain : a journal of neurology

Published: August 21, 2020

Factors Associated with Intergenerational Instability of ATXN3 CAG Repeat and Genetic Anticipation in Chinese Patients with Spinocerebellar Ataxia Type 3.

Factors Associated with Intergenerational Instability of ATXN3 CAG Repeat and Genetic Anticipation in Chinese Patients with Spinocerebellar Ataxia Type 3.

Journal: Cerebellum (London, England)

Published: July 18, 2020

Genotype-phenotype correlation in 667 Chinese families with spinocerebellar ataxia type 3.

Genotype-phenotype correlation in 667 Chinese families with spinocerebellar ataxia type 3.

Journal: Parkinsonism & related disorders

Published: April 26, 2020

Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3.

Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3.

Journal: Molecular genetics & genomic medicine

Published: February 08, 2020

The discriminative capacity of CSF β-amyloid 42 and Tau in neurodegenerative diseases in the Chinese population.

The discriminative capacity of CSF β-amyloid 42 and Tau in neurodegenerative diseases in the Chinese population.

Journal: Journal of the neurological sciences

Published: November 04, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026