Bing-wen Soong

No.201, Sec. 2, Shipai Rd
Taipei, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 78 publications

A dominant negative Kcnd3 F227del mutation in mice causes spinocerebellar ataxia type 22 (SCA22) by impairing ER and Golgi functioning.

A dominant negative Kcnd3 F227del mutation in mice causes spinocerebellar ataxia type 22 (SCA22) by impairing ER and Golgi functioning.

Journal: The Journal of pathology

Published: May 27, 2024

MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II.

MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II.

Journal: Heliyon

Published: September 06, 2023

Reply to: "Low Frequency of p.S510G in PIAS1 Challenges Its Relevance for Modifying Repeat Expansion Disorders".

Reply to: "Low Frequency of p.S510G in PIAS1 Challenges Its Relevance for Modifying Repeat Expansion Disorders".

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

Published: July 26, 2022

Scale for Ocular motor Disorders in Ataxia (SODA).

Scale for Ocular motor Disorders in Ataxia (SODA).

Journal: Journal of the neurological sciences

Published: July 05, 2022

Radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia.

Radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia.

Journal: Scientific reports

Published: March 09, 2022

COQ2 and SNCA polymorphisms interact with environmental factors to modulate the risk of multiple system atrophy and subtype disposition.

COQ2 and SNCA polymorphisms interact with environmental factors to modulate the risk of multiple system atrophy and subtype disposition.

Journal: European journal of neurology

Published: January 10, 2022

A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein Homeostasis.

A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein Homeostasis.

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

Published: July 28, 2021

Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation.

Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation.

Journal: International journal of molecular sciences

Published: July 11, 2021

Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.

Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.

Journal: Journal of the neurological sciences

Published: April 18, 2021

Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt KV4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties.

Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt KV4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties.

Journal: International journal of molecular sciences

Published: April 13, 2021

Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan.

Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan.

Journal: Parkinsonism & related disorders

Published: February 11, 2021

Investigating TBP CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS.

Investigating TBP CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: December 30, 2020

Showing 1-12 of 78

Last Updated: 09/26/2026