Rezultati - Kon‐Ping Lin

  • Showing 1 - 8 results of 8
Refine Results
  1. 1
    Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

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

    Izdano 2019
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  2. 2
    Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

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

    Izdano 2019
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  3. 3
    The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan

    The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan od Kon‐Ping Lin, Bing‐Wen Soong, Chih‐Chao Yang, Li-Wen Huang, Ming‐Hong Chang, I‐Hui Lee, Antony Antonellis, Yi‐Chung Lee

    Izdano 2011
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  4. 4
    PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions in a Taiwanese Cohort

    PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions in a Taiwanese Cohort od Yi‐Chung Lee, Ming‐Jen Lee, Hsiang‐Yu Yu, Chien Chen, Chang-Hung Hsu, Kon‐Ping Lin, Kwong‐Kum Liao, Ming‐Hong Chang, Yi‐Chu Liao, Bing‐Wen Soong

    Izdano 2012
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease

    Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease od Bing‐Wen Soong, Yen‐Hua Huang, Pei‐Chien Tsai, Chien‐Chang Huang, Hung-Chuan Pan, Yi-Chun Lu, Hsin-Ju Chien, Tze-Tze Liu, Ming-Hong Chang, Kon-Ping Lin, Pang‐Hsien Tu, Lung‐Sen Kao, Yi‐Chung Lee

    Izdano 2013
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  6. 6
    A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy

    A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy od Pei‐Chien Tsai, Bing‐Wen Soong, Inès Mademan, Yen‐Hua Huang, Chia-Rung Liu, Cheng‐Tsung Hsiao, Hung-Ta Wu, Tze-Tze Liu, Yo-Tsen Liu, Yen-Ting Tseng, Kon-Ping Lin, Ueng‐Cheng Yang, Ki Wha Chung, Byung‐Ok Choi, Garth A. Nicholson, Marina Kennerson, Chih‐Chiang Chan, Peter De Jonghe, Tzu-Hao Cheng, Yi‐Chu Liao, Stephan Züchner, Jonathan Baets, Yi‐Chung Lee

    Izdano 2017
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  7. 7
    Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis

    Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis od David Adams, Alejandra González‐Duarte, William O’Riordan, Chih‐Chao Yang, Mitsuharu Ueda, Arnt V. Kristen, Ivailo Tournev, Hartmut Schmidt, Teresa Coelho, John L. Berk, Kon-Ping Lin, Giuseppe Vita, Shahram Attarian, Violaine Planté‐Bordeneuve, Michelle M. Mezei, Josep M. Campistol, Juan Buades, Thomas H. Brannagan, Byoung J. Kim, Jeeyoung Oh, Yeşim Parman, Yoshiki Sekijima, Philip N. Hawkins, Scott D. Solomon, Michael Polydefkis, P. James B. Dyck, Pritesh J. Gandhi, Sunita Goyal, Jihong Chen, Andrew Strahs, Saraswathy V. Nochur, Marianne T. Sweetser, Pushkal Garg, Akshay Vaishnaw, Jared Gollob, Ole B. Suhr

    Izdano 2018
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  8. 8
    Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy

    Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy od Teresa Coelho, Wilson Marques, Noel R. Dasgupta, Chi‐Chao Chao, Yeşim Parman, Marcondes C. França, Yuh‐Cherng Guo, Jonas Wixner, Long‐Sun Ro, Cristian Calandra, Pedro André Kowacs, John L. Berk, Laura Obici, Fábio Barroso, Markus Weiler, Isabel Conceição, Shiangtung W. Jung, Gustavo Büchele, Michela Brambatti, Jersey Chen, Steven G. Hughes, Eugene Schneider, Nicholas J. Viney, Ahmad Masri, Morie R. Gertz, Yukio Ando, Julian D. Gillmore, Sami Khella, P. James B. Dyck, Márcia Waddington‐Cruz, Anna Mazzeo, Aikaterini Papagianni, Mazen M. Dimachkie, Ioannis Zaganas, Edward Gane, Marco Luigetti, Lucía Galán Dávila, Michelle M. Mezei, Juan González Moreno, Pascal Cintas, Davide Pareyson, Rebecca Traub, Julie Khoury, Conrado J. Estol, Merrilee Needham, David Adams, Michael Polydefkis, Thomas H. Brannagan, Vera Bril, Shahram Attarian, Marcelo Rugiero, B. Jane Distad, Eleni Zamba Papanicolaou, Kon‐Ping Lin, Merrill D. Benson, Morton Scheinberg

    Izdano 2023
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: