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Let-7g Improves Multiple Endothelial Functions Through Targeting Transforming Growth Factor-Beta and SIRT-1 Signaling

Journal of the American College of Cardiology, 2014-04, Vol.63 (16), p.1685-1694

2014

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

PloS one, 2015-08, Vol.10 (8), p.e0136501-e0136501

2015

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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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Subclinical Atherosclerosis Markers of Carotid Intima-Media Thickness, Carotid Plaques, Carotid Stenosis, and Mortality in Community-Dwelling Adults

International journal of environmental research and public health, 2020-07, Vol.17 (13), p.4745

2020

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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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Diameter Reduction Determined Through Carotid Ultrasound Associated With Cardiovascular and All-Cause Mortality: A Single-Center Experience of 38 201 Consecutive Patients in Taiwan

Journal of the American Heart Association, 2021-12, Vol.10 (23), p.e023689-e023689

2021

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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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Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

PloS one, 2017-05, Vol.12 (5), p.e0177296-e0177296

2017

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Population‐Based 5‐Year Follow‐Up Study in Taiwan of Osteoporosis and Risk of Periodontitis

Journal of periodontology (1970), 2014-03, Vol.85 (3), p.e24-e30

2014

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Indomethacin inhibits cancer cell migration via attenuation of cellular calcium mobilization

Molecules (Basel, Switzerland), 2013-06, Vol.18 (6), p.6584-6596

2013

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CASP3 gene single-nucleotide polymorphism (rs72689236) and Kawasaki disease in Taiwanese children

Journal of human genetics, 2011-02, Vol.56 (2), p.161-165

2011

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Use of a Smartphone Application to Speed Up Interhospital Transfer of Acute Ischemic Stroke Patients for Thrombectomy

Frontiers in neurology, 2021-05, Vol.12, p.606673-606673

2021

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Independent associations of urinary albumin-to-creatinine ratio and serum cystatin C with carotid intima-media thickness in community-living Taiwanese adults

BMC nephrology, 2020-10, Vol.21 (1), p.454-454, Article 454

2020

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Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy

Brain (London, England : 1878), 2022-09, Vol.145 (9), p.3010-3021

2022

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Intracerebral Hemorrhage in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prevalence, Clinical and Neuroimaging Features and Risk Factors

Stroke (1970), 2021-03, Vol.52 (3), p.985-993

2021

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Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy

JAMA : the journal of the American Medical Association, 2023-10, Vol.330 (15), p.1448

2023

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BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis

Molecular medicine (Cambridge, Mass.), 2011-09, Vol.17 (9-10), p.1065-1074

2011

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Association study of polymorphisms rs4552569 and rs17095830 and the risk of ankylosing spondylitis in a Taiwanese population

PloS one, 2013-01, Vol.8 (1), p.e52801-e52801

2013

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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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Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis

BMC medical genetics, 2010-06, Vol.11 (1), p.93-93, Article 93

2010

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Association of ORAI1 haplotypes with the risk of HLA-B27 positive ankylosing spondylitis

PloS one, 2011-06, Vol.6 (6), p.e20426-e20426

2011

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Olfactory Auras in Patients with Temporal Lobe Epilepsy

Epilepsia (Copenhagen), 2003-02, Vol.44 (2), p.257-260

2003

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Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization

Neurology, 2014-10, Vol.83 (17), p.1554-1561

2014

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Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke

BMC medical genetics, 2013-01, Vol.14 (1), p.17-17, Article 17

2013

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Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia

Parkinsonism & related disorders, 2022-10, Vol.103, p.144-149

2022

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Let-7g Improves Multiple Endothelial Functions Through Targeting Transforming Growth Factor-Beta and SIRT-1 Signaling

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

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

Subclinical Atherosclerosis Markers of Carotid Intima-Media Thickness, Carotid Plaques, Carotid Stenosis, and Mortality in Community-Dwelling Adults

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

Diameter Reduction Determined Through Carotid Ultrasound Associated With Cardiovascular and All-Cause Mortality: A Single-Center Experience of 38 201 Consecutive Patients in Taiwan

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

Population‐Based 5‐Year Follow‐Up Study in Taiwan of Osteoporosis and Risk of Periodontitis

Indomethacin inhibits cancer cell migration via attenuation of cellular calcium mobilization

CASP3 gene single-nucleotide polymorphism (rs72689236) and Kawasaki disease in Taiwanese children

Use of a Smartphone Application to Speed Up Interhospital Transfer of Acute Ischemic Stroke Patients for Thrombectomy

Independent associations of urinary albumin-to-creatinine ratio and serum cystatin C with carotid intima-media thickness in community-living Taiwanese adults

Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy

Intracerebral Hemorrhage in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prevalence, Clinical and Neuroimaging Features and Risk Factors

Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy

BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis

Association study of polymorphisms rs4552569 and rs17095830 and the risk of ankylosing spondylitis in a Taiwanese population

Clinical and biophysical characterization of 19 GJB1 mutations

Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis

Association of ORAI1 haplotypes with the risk of HLA-B27 positive ankylosing spondylitis

Olfactory Auras in Patients with Temporal Lobe Epilepsy

Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization

Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke

Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia

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