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Annals of Clinical and Translational Neurology
|
April 23, 2024
Genetic analysis of IRF2BPL in a Taiwanese dystonia cohort: The genotype and phenotype correlation
Pin-Shiuan Chen, Ying-Fa Chen, Jian-Ying Chiu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
December 6, 2025
Parkinson's disease in transition: Genetics, biomarkers, and emerging therapeutics
Sung-Pin Fan, Ayami Okuzumi, Pin-Shiuan Chen, et al.
Journal of Neuromuscular Diseases
|
April 17, 2023
Diagnostic Challenges of Neuromuscular Disorders after Whole Exome Sequencing
Pin-Shiuan Chen, Chi-Chao Chao, Li-Kai Tsai, et al.
Neurology
|
December 12, 2025
Plasma pTau217 and Neurofilament Light Chain as Differentiative Markers for Progressive Supranuclear Palsy From Parkinson Disease
Cheng-Hsuan Li, Sung-Pin Fan, Pin-Shiuan Chen, et al.
Diseases (Basel, Switzerland)
|
August 27, 2025
Ten-Year Trends in Hepatocellular Carcinoma Mortality: Examining the Interaction Between Fibrosis Score and Patient Age
Ayrton Bangolo, Hadrian Hoang-Vu Tran, Budoor Alqinai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 28, 2025
Neuronal-specific antibody in patients with multiple system atrophy and progressive supranuclear palsy
Mimi S Fang, Ming-Chen Tsai, Friederike A Arlt, et al.
World Journal of Clinical Oncology
|
July 1, 2024
Characteristics and distinct prognostic determinants of individuals with hepatosplenic T-cell lymphoma over the past two decades
Ayrton Bangolo, Pierre Fwelo, Shraboni Dey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 27, 2023
Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5
Pin-Shiuan Chen, Ni-Chung Lee, Chieh-Ju Sung, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 29, 2025
Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly Individuals
Pin-Shiuan Chen, Yi-Ling Liu, Pu-Tien Chiang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Is <i>SORL1</i> a common genetic target across neurodegenerative diseases?: A multi-ancestry biobank scale assessment
Marzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.
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Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Annals of Clinical and Translational Neurology
|
April 23, 2024
Genetic analysis of IRF2BPL in a Taiwanese dystonia cohort: The genotype and phenotype correlation
Pin-Shiuan Chen, Ying-Fa Chen, Jian-Ying Chiu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
December 6, 2025
Parkinson's disease in transition: Genetics, biomarkers, and emerging therapeutics
Sung-Pin Fan, Ayami Okuzumi, Pin-Shiuan Chen, et al.
Journal of Neuromuscular Diseases
|
April 17, 2023
Diagnostic Challenges of Neuromuscular Disorders after Whole Exome Sequencing
Pin-Shiuan Chen, Chi-Chao Chao, Li-Kai Tsai, et al.
Neurology
|
December 12, 2025
Plasma pTau217 and Neurofilament Light Chain as Differentiative Markers for Progressive Supranuclear Palsy From Parkinson Disease
Cheng-Hsuan Li, Sung-Pin Fan, Pin-Shiuan Chen, et al.
Diseases (Basel, Switzerland)
|
August 27, 2025
Ten-Year Trends in Hepatocellular Carcinoma Mortality: Examining the Interaction Between Fibrosis Score and Patient Age
Ayrton Bangolo, Hadrian Hoang-Vu Tran, Budoor Alqinai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 28, 2025
Neuronal-specific antibody in patients with multiple system atrophy and progressive supranuclear palsy
Mimi S Fang, Ming-Chen Tsai, Friederike A Arlt, et al.
World Journal of Clinical Oncology
|
July 1, 2024
Characteristics and distinct prognostic determinants of individuals with hepatosplenic T-cell lymphoma over the past two decades
Ayrton Bangolo, Pierre Fwelo, Shraboni Dey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 27, 2023
Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5
Pin-Shiuan Chen, Ni-Chung Lee, Chieh-Ju Sung, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 29, 2025
Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly Individuals
Pin-Shiuan Chen, Yi-Ling Liu, Pu-Tien Chiang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Is <i>SORL1</i> a common genetic target across neurodegenerative diseases?: A multi-ancestry biobank scale assessment
Marzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.
Page
of 3