Publications by authors named "Kon-Ping Lin"

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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, Cheng-Hsuan Tsai, Mao-Yuan Su, Kon-Ping Lin, Yen-Hung Lin

J Formos Med Assoc· April 2025

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Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study.
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, Ming-Jen Lee, John Vest

J Formos Med Assoc· September 2024

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Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy.
Laura Obici, Senda Ajroud-Driss, Kon-Ping Lin, John L Berk, Julian D Gillmore

Neurol Ther· October 2023

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Clinical and genetic characterization of NEFL-related neuropathy in Taiwan.
Hua-Chuan Chao, Cheng-Tsung Hsiao, Kuan-Lin Lai, Yu-Shuen Tsai, Kon-Ping Lin

J Formos Med Assoc· February 2023

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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.
Kang-Yang Jih, Kuan-Lin Lai, Kon-Ping Lin, Yi-Chu Liao, Yi-Chung Lee

J Chin Med Assoc· January 2023

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Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia.
Shao-Lun Hsu, Yi-Chu Liao, Kon-Ping Lin, Po-Yu Lin, Kai-Wei Yu

Parkinsonism Relat Disord· October 2022

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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, Ching-Piao Tsai, Jong-Ling Fuh, Kon-Ping Lin

J Formos Med Assoc· September 2022

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Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia.
Shao-Lun Hsu, Kang-Yang Jih, Kon-Ping Lin, Yi-Chu Liao, Yi-Chung Lee

Parkinsonism Relat Disord· March 2022

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GGC Repeat Expansion of in Taiwanese Patients With Inherited Neuropathies.
Yi-Chu Liao, Fu-Pang Chang, Han-Wei Huang, Ting-Bing Chen, Ying-Tsen Chou, Kon-Ping Lin, Chou-Ching K Lin

Neurology· January 2022

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Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis.
Pei-Chien Tsai, Kang-Yang Jih, Ting-Yi Shen, Yi-Hong Liu, Kon-Ping Lin

Neurol Genet· December 2021

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Investigating CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS.
Kang-Yang Jih, Kon-Ping Lin, Pei-Chien Tsai, Bing-Wen Soong, Yi-Chu Liao

Amyotroph Lateral Scler Frontotemporal Degener· August 2021

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Hereditary transthyretin amyloidosis in multi-ethnic Malaysians.
Soon-Chai Low, Nor Ashikin Md Sari, Cheng-Yin Tan, Azlina Ahmad-Annuar, Kum-Thong Wong, Kon-Ping Lin

Neuromuscul Disord· July 2021

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Comparison of Corticosteroid Injection Dosages in Mild to Moderate Idiopathic Carpal Tunnel Syndrome: A Randomized Controlled Trial.
Po-Cheng Hsu, Kwong-Kum Liao, Kon-Ping Lin, Jan-Wei Chiu, Pin-Yi Wu

Arch Phys Med Rehabil· November 2020

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Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant.
Yu-Shuen Tsai, Kon-Ping Lin, Kang-Yang Jih, Pei-Chien Tsai, Yi-Chu Liao

Ann Clin Transl Neurol· June 2020

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Reply to "Use DN4-T to rule out non-neuropathic pain".
Yen-Feng Wang, Chih-Chao Yang, Long-Sun Ro, Yu-Chuan Tsai, Kon-Ping Lin

J Chin Med Assoc· May 2020

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Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration.
Ridwan Babatunde Ibrahim, Ssu-Yu Yeh, Kon-Ping Lin, Frans Ricardo, Tsyr-Yan Yu

Cell Mol Life Sci· April 2020

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Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5.
Cheng-Ta Chou, Bing-Wen Soong, Kon-Ping Lin, Yu-Shuen Tsai, Kang-Yang Jih

Ann Clin Transl Neurol· April 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.
Long-Sun Ro, Chih-Chao Yang, Rong-Kuo Lyu, Kon-Ping Lin, Tzung-Chang Tsai

PLoS One· February 2020

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Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy.
Soon Chai Low, Cheng Yin Tan, Nor Ashikin Md Sari, Azlina Ahmad-Annuar, Kum Thong Wong, Kon-Ping Lin

Amyloid· January 2020

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Biophysical characterization and modulation of Transthyretin Ala97Ser.
Yo-Tsen Liu, Yueh-Jung Yen, Frans Ricardo, Yu Chang, Pei-Hao Wu, Kon-Ping Lin

Ann Clin Transl Neurol· October 2019

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Development and validation of a Taiwan version of the DN4-T questionnaire.
Yen-Feng Wang, Chih-Chao Yang, Long-Sun Ro, Yu-Chuan Tsai, Kon-Ping Lin

J Chin Med Assoc· August 2019

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Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan.
Yun-Hsin Hsu, Kon-Ping Lin, Yuh-Cherng Guo, Yu-Shuen Tsai, Yi-Chu Liao

Ann Clin Transl Neurol· June 2019

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Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan.
Hua-Chuan Chao, Yi-Chu Liao, Yo-Tsen Liu, Yuh-Cherng Guo, Fu-Pang Chang, Kon-Ping Lin

Ann Clin Transl Neurol· May 2019

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Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan.
Pei-Chien Tsai, Yi-Chu Liao, Kang-Yang Jih, Bing-Wen Soong, Kon-Ping Lin

Neurobiol Aging· December 2018

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Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis.
David Adams, Alejandra Gonzalez-Duarte, William D O'Riordan, Chih-Chao Yang, Mitsuharu Ueda, Kon-Ping Lin

N Engl J Med· July 2018

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