B. Soong

Po-Shan Wang, Chih-I Hung, Shin Teng, 2008, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Octarepeat changes of prion protein in Parkinson's disease.

Bing-Wen Soong, M. Kao, Vinchi Wang, 2009, Parkinsonism & related disorders.

SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications.

H. Fung, Yih-Ru Wu, C. Chen, 2010, Clinica chimica acta; international journal of clinical chemistry.

Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.

Bing-Wen Soong, K. Choo, Yi-Chun Lu, 2001 .

A randomized controlled pilot trial of game-based training in individuals with spinocerebellar ataxia type 3

Yea-Ru Yang, Ray-Yau Wang, B. Soong, 2018, Scientific Reports.

DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.

K. Hsiao, B. Soong, T. Su, 1991, American journal of medical genetics.

Val-9Ala and Ile+58Thr polymorphism of MnSOD in Parkinson's disease.

M. Kao, B. Soong, Shao-Yuan Chen, 2010, Clinical biochemistry.

Clinical and biophysical characterization of 19 GJB1 mutations

P. Tsai, Yi-Chung Lee, Y. Liao, 2016, Annals of clinical and translational neurology.

Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth disease

Yi-Chung Lee, Ming-Wei Lin, Ming-Hong Chang, 2010, Neuromuscular Disorders.

5′-Flanking region polymorphism of the neuronal nitric oxide synthase gene with Parkinson's disease in Taiwan

E. Hogan, B. Soong, H. Lo, 2002, Journal of the Neurological Sciences.

Mutations in the Novel Protein PRRT2 Cause Infantile Convulsions with Paroxysmal Kinesigenic Dyskinesia

Lynch, J. Jankovic, A. Bowcock, 2012 .

Medical and Paramedical Care of Patients With Cerebellar Ataxia During the COVID-19 Outbreak: Seven Practical Recommendations of the COVID 19 Cerebellum Task Force

H. Mitoma, M. Molinari, J. Schmahmann, 2020, Frontiers in Neurology.

A Pilot Study of a New Thrombolytic Agent for Acute Ischemic Stroke in Taiwan Within A Five-Hour Window

Y. Luk, W. Wong, Han-Hwa Hu, 2006, Stroke.

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

P. Tsai, Yi-Chung Lee, Y. Liao, 2017, Journal of the Neurological Sciences.

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Yi-Chung Lee, Y. Liao, B. Soong, 2020, Annals of clinical and translational neurology.

Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in Taiwan

Y. Liao, B. Soong, M. Lan, 2018, Clinical genetics.

Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis

P. Tsai, Yi-Chung Lee, Y. Liao, 2018, Neurobiology of Aging.

Fractal dimension analysis for quantifying cerebellar morphological change of multiple system atrophy of the cerebellar type (MSA-C)

Kuo-Kai Shyu, Po-Shan Wang, Yu-Te Wu, 2010, NeuroImage.

Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles

Wei‐Ju Lee, Yi-Chung Lee, Yen-Feng Wang, 2015, PloS one.

Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6

B. Soong, P.-S. Wang, R.-S. Liu, 2007, Journal of Neurology.

Comparison of cerebellar ataxias: A three‐year prospective longitudinal assessment

Po-Shan Wang, Yi-Chung Lee, Y. Liao, 2011, Movement disorders : official journal of the Movement Disorder Society.

Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan

Yi-Chung Lee, Y. Liao, B. Soong, 2020, The Cerebellum.

Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington's disease patients.

Yih-Ru Wu, M. Cheng, D. Chiu, 2007, Biochemical and biophysical research communications.

Age at onset prediction in spinocerebellar ataxia type 3 changes according to population of origin

M. Saraiva-Pereira, M. Lima, S. Camey, 2018, European journal of neurology.

Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan

Yi-Chung Lee, Y. Liao, B. Soong, 2020, The Cerebellum.

SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications

H. Fung, Yih-Ru Wu, C. Chen, 2009, Human Genetics.

Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications

Ren-Shyan Liu, K. Liao, B. Soong, 2004, Movement disorders : official journal of the Movement Disorder Society.

Spinocerebellar ataxia type 2 presenting as familial levodopa‐responsive parkinsonism

Changming Sun, K. Liao, B. Soong, 2001, Annals of neurology.

Disrupted cerebellar connectivity reduces whole‐brain network efficiency in multiple system atrophy

Shin Teng, Chia-Feng Lu, Po-Shan Wang, 2013, Movement disorders : official journal of the Movement Disorder Society.

Differences between Spinocerebellar Ataxias and Multiple System Atrophy-Cerebellar Type on Proton Magnetic Resonance Spectroscopy

Po-Shan Wang, J. Lirng, Wan-Yuo Guo, 2012, PloS one.

Quantifying cerebellar atrophy in multiple system atrophy of the cerebellar type (MSA-C) using three-dimensional gyrification index analysis

Yu-Te Wu, Kuo-Kai Shyu, Tzu-Yun Wang, 2012, NeuroImage.

Hereditary spinocerebellar ataxias: number, prevalence, and treatment prospects.

B. Soong, 2004, Hong Kong medical journal = Xianggang yi xue za zhi.

Intra- and Inter-Modular Connectivity Alterations in the Brain Structural Network of Spinocerebellar Ataxia Type 3

Yu-Te Wu, Tzu-Yun Wang, Po-Shan Wang, 2019, Entropy.

A novel DNAJB6 mutation causes dominantly inherited distal‐onset myopathy and compromises DNAJB6 function

P. Tsai, Y. Liao, B. Soong, 2017, Clinical genetics.

Cerebral involvement in spinal and bulbar muscular atrophy (Kennedy's disease): A pilot study of PET

Po-Shan Wang, Yi-Chung Lee, Ren-Shyan Liu, 2013, Journal of the Neurological Sciences.

Dentatorubropallidoluysian atrophy in Chinese.

Yue-Cune Chang, B. Soong, Yi-Chun Lu, 2001, Archives of neurology.

SCA 8 repeat expansion : large CTA / CTG repeat alleles in neurological disorders and functional implications

H. Fung, Yih-Ru Wu, C. Chen, 2009 .

Sleep disruption in spinocerebellar ataxia type 3: A genetic and polysomnographic study

Hsiao-Lun Ku, B. Soong, N. Chi, 2013, Journal of the Chinese Medical Association : JCMA.

Management of Patients with Cerebellar Ataxia During the COVID-19 Pandemic: Current Concerns and Future Implications

H. Mitoma, M. Molinari, J. Schmahmann, 2020, The Cerebellum.

Intravenous Administration of Allogeneic Mesenchymal Stem Cells in Patients with Cerebellar Ataxias: A Phase I/IIa Clinical Trial

O. Lee, B. Soong, K. Ho, 2016 .

Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

D. Labuda, M. Pandolfo, J. Poirier, 2000, Neurology.

Characterization of the cea gene of the ColE7 plasmid.

K. Chak, B. Soong, F. Lu, 1992, Molecular & general genetics : MGG.

Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy

P. Tsai, Yi-Chung Lee, Yen‐Hua Huang, 2016, PloS one.

MPZ mutation G123S characterization

B. Soong, M. Chang, Y. Liu, 2008, Neurology.

Management of Patients with Cerebellar Ataxia During the COVID-19 Pandemic: Current Concerns and Future Implications

H. Mitoma, M. Molinari, J. Schmahmann, 2020, Cerebellum.

Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan

P. Tsai, Yi-Chung Lee, Y. Liao, 2018, Neurobiology of Aging.

Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases

S. Kuo, Yau-Huei Wei, B. Soong, 2008, Journal of the Neurological Sciences.

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

P. Gonzalez-Alegre, T. Bardakjian, T. Tropea, 2021, International journal of molecular sciences.

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

A. Capuano, S. Servidei, G. Zanni, 2021, International journal of molecular sciences.

Dysregulated brain creatine kinase is associated with hearing impairment in mouse models of Huntington disease.

P. Poon, Yih-Ru Wu, Y. Chern, 2011, The Journal of clinical investigation.

Novel SCA19/22‐associated KCND3 mutations disrupt human KV4.3 protein biosynthesis and channel gating

Yo-Tsen Liu, B. Soong, Ssu-Ju Fu, 2019, Human mutation.

Spastic paraparesis as a manifestation of metabolic vitamin B12 deficiency

B. Soong, Y-C Lee, Sheng-Hsiung Cheng, 2005, Journal of Neurology.

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

Yi-Chung Lee, Y. Liao, J. Fuh, 2021, Journal of Neurological Sciences.

Multiple sulfatase deficiency

J. Fink, G. Constantopoulos, B. Soong, 1988, Neurology.

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

Yi-Chung Lee, Y. Chern, Tzu-Hao Cheng, 2022, Movement disorders : official journal of the Movement Disorder Society.

Genetic screening for Huntington's disease in Chinese patients with involuntary movements

Zin-An Wu, B. Soong, D. Shan, 1997, Clinical Neurology and Neurosurgery.

An electrophysiologic and pathologic study of peripheral nerves in individuals with Machado-Joseph disease.

B. Soong, K. Lin, 1998, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.

The remarkably variable expressivity of CADASIL: report of a minimally symptomatic man at an advanced age

Yi-Chung Lee, B. Soong, A. Yang, 2009, Journal of Neurology.

A comparison of the Huntington's disease associated trinucleotide repeat between Chinese and white populations.

B. Soong, J. T. Wang, 1995, Journal of medical genetics.

Metabolic characterization of spinocerebellar ataxia type 6.

Ren-Shyan Liu, B. Soong, Liang-Chih Wu, 2001, Archives of neurology.

Splice isoform-specific suppression of the CaV2.1 variant underlying spinocerebellar ataxia type 6

H. Paulson, B. Soong, Wei-Ling Tsou, 2011, Neurobiology of Disease.