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Annals of Clinical and Translational Neurology
|
November 16, 2016
Clinical and biophysical characterization of 19 <i>GJB1</i> mutations
Pei-Chien Tsai, De-Ming Yang, Yi-Chu Liao, et al.
Clinical Neurology and Neurosurgery
|
March 21, 2008
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
Shyue-Ru Chen, Kon-Ping Lin, Hung-Chou Kuo, et al.
American Journal of Human Genetics
|
February 26, 2013
Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease
Bing-Wen Soong, Yen-Hua Huang, Pei-Chien Tsai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 22, 2021
Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder
Yi-Hong Liu, Yuh-Cherng Guo, Lien-Ying Lin, et al.
Neurology
|
August 8, 2014
A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function
Pei-Chien Tsai, Yen-Hua Huang, Yuh-Cherng Guo, et al.
Neurology
|
October 22, 2021
GGC Repeat Expansion of <i>NOTCH2NLC</i> in Taiwanese Patients With Inherited Neuropathies
Yi-Chu Liao, Fu-Pang Chang, Han-Wei Huang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 10, 2024
Use of technetium-99m-pyrophosphate single-photon emission computed tomography/computed tomography in monitoring therapeutic changes of RNA interference therapeutics in patients with hereditary transthyretin amyloid cardiomyopathy
Yi-Hsin Hung, An-Li Yu, Yi-Chieh Chen, et al.
Brain : a Journal of Neurology
|
April 4, 2017
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy
Pei-Chien Tsai, Bing-Wen Soong, Inès Mademan, et al.
The New England Journal of Medicine
|
July 5, 2018
Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
David Adams, Alejandra Gonzalez-Duarte, William D O'Riordan, et al.
Acta Neurologica Taiwanica
|
April 25, 2026
Taiwan Clinical Practice Guidelines for Myasthenia Gravis
Hsu-Ling Yeh, Che-Cheng Chang, An-Bang Liu, et al.
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Search research articles
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Showing results (71-80 of 80) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 80 results.
Annals of Clinical and Translational Neurology
|
November 16, 2016
Clinical and biophysical characterization of 19 <i>GJB1</i> mutations
Pei-Chien Tsai, De-Ming Yang, Yi-Chu Liao, et al.
Clinical Neurology and Neurosurgery
|
March 21, 2008
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
Shyue-Ru Chen, Kon-Ping Lin, Hung-Chou Kuo, et al.
American Journal of Human Genetics
|
February 26, 2013
Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease
Bing-Wen Soong, Yen-Hua Huang, Pei-Chien Tsai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 22, 2021
Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder
Yi-Hong Liu, Yuh-Cherng Guo, Lien-Ying Lin, et al.
Neurology
|
August 8, 2014
A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function
Pei-Chien Tsai, Yen-Hua Huang, Yuh-Cherng Guo, et al.
Neurology
|
October 22, 2021
GGC Repeat Expansion of <i>NOTCH2NLC</i> in Taiwanese Patients With Inherited Neuropathies
Yi-Chu Liao, Fu-Pang Chang, Han-Wei Huang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 10, 2024
Use of technetium-99m-pyrophosphate single-photon emission computed tomography/computed tomography in monitoring therapeutic changes of RNA interference therapeutics in patients with hereditary transthyretin amyloid cardiomyopathy
Yi-Hsin Hung, An-Li Yu, Yi-Chieh Chen, et al.
Brain : a Journal of Neurology
|
April 4, 2017
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy
Pei-Chien Tsai, Bing-Wen Soong, Inès Mademan, et al.
The New England Journal of Medicine
|
July 5, 2018
Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
David Adams, Alejandra Gonzalez-Duarte, William D O'Riordan, et al.
Acta Neurologica Taiwanica
|
April 25, 2026
Taiwan Clinical Practice Guidelines for Myasthenia Gravis
Hsu-Ling Yeh, Che-Cheng Chang, An-Bang Liu, et al.
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of 8