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A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1252-1266

2017

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The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan

PloS one, 2011-12, Vol.6 (12), p.e29393-e29393

2011

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Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration

Cellular and molecular life sciences : CMLS, 2020-04, Vol.77 (7), p.1421-1434

2020

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A prospective, observational study on conversion of clinically isolated syndrome to multiple sclerosis during 4-year period (MS NEO study) in Taiwan

PloS one, 2019-07, Vol.14 (7), p.e0202453-e0202453

2019

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Sonographic median nerve change after steroid injection for carpal tunnel syndrome

Muscle & nerve, 2018-09, Vol.58 (3), p.402-406

2018

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Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study

Journal of the Formosan Medical Association, 2024-09, Vol.123 (9), p.975-984

2024

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Lead, Mercury, and Arsenic Poisoning Due to Topical Use of Traditional Chinese Medicines

The American journal of medicine, 2013-05, Vol.126 (5), p.451-454

2013

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

PloS one, 2016-01, Vol.11 (1), p.e0147677

2016

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Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder

Journal of the Formosan Medical Association, 2022-09, Vol.121 (9), p.1647-1656

2022

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

Movement disorders, 2011-09, Vol.26 (11), p.2081-2087

2011

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PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort

PloS one, 2012-08, Vol.7 (8), p.e38543-e38543

2012

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Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

Annals of clinical and translational neurology, 2019-06, Vol.6 (6), p.1090-1101

2019

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Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy

Scientific reports, 2017-11, Vol.7 (1), p.15363-9, Article 15363

2017

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Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Annals of clinical and translational neurology, 2019-05, Vol.6 (5), p.913-922

2019

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Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Annals of clinical and translational neurology, 2020-04, Vol.7 (4), p.486-496

2020

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Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant

Annals of clinical and translational neurology, 2020-06, Vol.7 (6), p.965-971

2020

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Biophysical characterization and modulation of Transthyretin Ala97Ser

Annals of clinical and translational neurology, 2019-10, Vol.6 (10), p.1961-1970

2019

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

Journal of the neurological sciences, 2013-12, Vol.335 (1), p.139-144

2013

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GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies

Neurology, 2022-01, Vol.98 (2), p.e199

2022

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A proposed mechanism of superficial siderosis supported by surgical and neuroimaging findings

Medical hypotheses, 2011-06, Vol.76 (6), p.823-826

2011

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Comparison of Corticosteroid Injection Dosages in Mild to Moderate Idiopathic Carpal Tunnel Syndrome: A Randomized Controlled Trial

Archives of physical medicine and rehabilitation, 2020-11, Vol.101 (11), p.1857-1864

2020

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Clinical and biophysical characterization of 19 GJB1 mutations

Annals of clinical and translational neurology, 2016-11, Vol.3 (11), p.854-865

2016

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Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis

Neurobiology of aging, 2016-04, Vol.40, p.191.e11-191.e16

2016

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Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia

Parkinsonism & related disorders, 2022-03, Vol.96, p.43-44

2022

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Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis

Journal of the Chinese Medical Association, 2023-01, Vol.86 (1), p.47-51

2023

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A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy

The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan

Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration

A prospective, observational study on conversion of clinically isolated syndrome to multiple sclerosis during 4-year period (MS NEO study) in Taiwan

Sonographic median nerve change after steroid injection for carpal tunnel syndrome

Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study

Lead, Mercury, and Arsenic Poisoning Due to Topical Use of Traditional Chinese Medicines

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

Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder

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

PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort

Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant

Biophysical characterization and modulation of Transthyretin Ala97Ser

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

GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies

A proposed mechanism of superficial siderosis supported by surgical and neuroimaging findings

Comparison of Corticosteroid Injection Dosages in Mild to Moderate Idiopathic Carpal Tunnel Syndrome: A Randomized Controlled Trial

Clinical and biophysical characterization of 19 GJB1 mutations

Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis

Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia

Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis

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