Torthaí cuardaigh - Shuan‐Pei Lin

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  1. 1
    Assessing the impact of the five senses on quality of life in mucopolysaccharidoses

    Assessing the impact of the five senses on quality of life in mucopolysaccharidoses de réir Roberto Giugliani, Paul Harmatz, Shuan‐Pei Lin, Maurizio Scarpa

    Foilsithe / Cruthaithe 2020
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  2. 2
    MPS screening methods, the berry spot and acid turbidity tests, cause a high incidence of false‐negative results in sanfilippo and morquio syndromes

    MPS screening methods, the berry spot and acid turbidity tests, cause a high incidence of false‐negative results in sanfilippo and morquio syndromes de réir Chih‐Kuang, Chang, Shuan‐Pei, Lin, Shyue‐Jye, Lee, Tuen‐Jen, Wang

    Foilsithe / Cruthaithe 2002
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  3. 3
    A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses

    A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses de réir Chih‐Kuang Chuang, Hsiang‐Yu Lin, Tuen-Jen Wang, Chia‐Chen Tsai, Hsuan‐Liang Liu, Shuan‐Pei Lin

    Foilsithe / Cruthaithe 2014
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  4. 4
    Understanding Genetic Screening: Harnessing Health Information to Prevent Disease Risks

    Understanding Genetic Screening: Harnessing Health Information to Prevent Disease Risks de réir Chung‐Lin Lee, Chih‐Kuang Chuang, Huei‐Ching Chiu, Ya-Hui Chang, Yuan-Rong Tu, Yun‐Ting Lo, Hsiang‐Yu Lin, Shuan‐Pei Lin

    Foilsithe / Cruthaithe 2025
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  5. 5
    Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria

    Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria de réir Mei‐Ying Liu, Yan-Ling Yang, Ying-Chen Chang, Szu-Hui Chiang, Shuan-Pei Lin, Lian-Shu Han, Yu Qi, Kwang-Jen Hsiao, Tze-Tze Liu

    Foilsithe / Cruthaithe 2010
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  6. 6
    A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan

    A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan de réir Shuan‐Pei Lin, Hsiang‐Yu Lin, Tuen-Jen Wang, Chia-Ying Chang, Chia-Hui Lin, Sung‐Fa Huang, Chia‐Chen Tsai, Hsuan‐Liang Liu, Joan Keutzer, Chih‐Kuang Chuang

    Foilsithe / Cruthaithe 2013
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  7. 7
    The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects

    The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects de réir Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Carla E. M. Hollak, Peter Slasor, Celeste Decker

    Foilsithe / Cruthaithe 2013
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  8. 8
    Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI

    Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI de réir Min-Ju Chan, Hsuan-Chieh Liao, Michael H. Gelb, Chih‐Kuang Chuang, Mei‐Ying Liu, Hsiao-Jan Chen, Shu‐Min Kao, Hsiang‐Yu Lin, You-Hsin Huang, Arun Kumar, Naveen Kumar Chennamaneni, Nagendar Pendem, Shuan‐Pei Lin, Chuan-Chi Chiang

    Foilsithe / Cruthaithe 2018
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  9. 9
    Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of <i>GALNS</i> gene variants and reporting of 68 novel variants

    Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of <i>GALNS</i> gene variants and reporting of 68 novel variants de réir Alessandra Zanetti, Francesca D’Avanzo, Moeenaldeen AlSayed, Ana Carolina Brusius‐Facchin, Yin‐Hsiu Chien, Roberto Giugliani, Emanuela Izzo, David C. Kasper, Hsiang‐Yu Lin, Shuan‐Pei Lin, Laura Pollard, Akashdeep Singh, Rodolfo Tonin, Tim Wood, Amelia Morrone, Rosella Tomanin

    Foilsithe / Cruthaithe 2021
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  10. 10
    Longitudinal analysis of endurance and respiratory function from a natural history study of Morquio A syndrome

    Longitudinal analysis of endurance and respiratory function from a natural history study of Morquio A syndrome de réir Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Frits A. Wijburg, Kehu Yang, Peter Slasor, Celeste Decker

    Foilsithe / Cruthaithe 2014
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  11. 11
    Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure

    Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure de réir Minke H. de Ru, Q. Teunissen, Johanna H. van der Lee, Michael Beck, Olaf A. Bodamer, Lorne A. Clarke, Carla E. M. Hollak, Shuan-Pei Lin, M. Rojas, Gregory M. Pastores, Julian Raiman, Maurizio Scarpa, Eileen P. Treacy, Anna Tylki‐Szymańska, J. E. Wraith, J Zeman, Frits A. Wijburg

    Foilsithe / Cruthaithe 2012
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  12. 12
    Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups

    Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups de réir Tzu-Hung Chu, Yin‐Hsiu Chien, Hsiang‐Yu Lin, Hsuan-Chieh Liao, Huey-Jane Ho, Chih-Jou Lai, Chuan-Chi Chiang, Niang‐Cheng Lin, Chia-Feng Yang, Wuh‐Liang Hwu, Ni‐Chung Lee, Shuan-Pei Lin, Chin-Su Liu, Rey‐Heng Hu, Ming‐Chih Ho, Dau-Ming Niu

    Foilsithe / Cruthaithe 2019
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  13. 13
    Longitudinal Natural History of Pediatric Subjects Affected with Mucopolysaccharidosis IIIB

    Longitudinal Natural History of Pediatric Subjects Affected with Mucopolysaccharidosis IIIB de réir İlyas Okur, Fatih Süheyl Ezgü, Roberto Giugliani, Nicole Muschol, Anja F. Koehn, Hernán Amartino, Paul Harmatz, María José de Castro López, María L. Couce, Shuan‐Pei Lin, Spyros Batzios, Maureen Cleary, Martha Solano, Heidi Peters, Joy Lee, Igor Nestrašil, Adam J. Shaywitz, Stephen M. Maricich, Bernice Kuca, Joseph Kovalchin, Eric Zanelli

    Foilsithe / Cruthaithe 2022
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  14. 14
    Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese

    Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese de réir Mullin H.C. Yu, Mandy Ho-Yin Tsang, Sophie Lai, Matthew Sai-pong Ho, Donald Tse, Brooke Willis, Anna Ka‐Yee Kwong, Yen-Yin Chou, Shuan-Pei Lin, Catarina M. Quinzii, Wuh‐Liang Hwu, Yin‐Hsiu Chien, Pao‐Lin Kuo, C. Chan, Cheung Tsoi, Shuk-Ching Chong, Richard J. Rodenburg, Jan Smeitink, Christopher Chun Yu Mak, Kit San Yeung, Jasmine Lee-Fong Fung, Wendy Lam, Joannie Hui, Ni‐Chung Lee, Cheuk‐Wing Fung, Brian Hon‐Yin Chung

    Foilsithe / Cruthaithe 2019
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  15. 15
    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly de réir Daniela A. Braun, Jia Rao, Géraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst‐Schwan, Johanna Magdalena Schmidt, Jennifer A. Lawson, Denny Schanze, Shazia Ashraf, Jeremy F.P. Ullmann, Charlotte A. Hoogstraten, Nathalie Boddaert, Bruno Collinet, Gaëlle Martin, Dominique Liger, Svjetlana Lovric, Mónica Furlano, Ida Chiara Guerrera, Oraly Sanchez-Ferras, Jennifer Hu, Anne‐Claire Boschat, Sylvia Sanquer, Björn Menten, Sarah Vergult, Nina De Rocker, Merlin Airik, Tobias Hermle, Shirlee Shril, Eugen Widmeier, Heon Yung Gee, Won‐Il Choi, Carolin E. Sadowski, Werner L. Pabst, Jillian K. Warejko, Ankana Daga, Tamara Basta, Verena Matejas, Karin Scharmann, Sandra D. Kienast, Babak Behnam, Brendan Beeson, Amber Begtrup, M. Bruce, Gaik-Siew Ch’ng, Shuan‐Pei Lin, Jui-Hsing Chang, Chao‐Huei Chen, Megan T. Cho, Patrick M. Gaffney, Patrick Gipson, Chyong-Hsin Hsu, Jameela A. Kari, Yu-Yuan Ke, Cathy Kiraly‐Borri, Wai-ming Lai, Emmanuelle Lemyre, Rebecca O. Littlejohn, Amira Masri, Mastaneh Moghtaderi, Kazuyuki Nakamura, Fatih Özaltın, Marleen Praet, Chitra Prasad, Agnieszka Prytula-Ebels, Elizabeth Roeder, Patrick Rump, Rhonda E. Schnur, Takashi Shiihara, Manish D. Sinha, Neveen A. Soliman, Kenza Soulami, David A. Sweetser, Wen‐Hui Tsai, Jeng-Daw Tsai, Rezan Topaloĝlu, Udo Vester, David H. Viskochil, Nithiwat Vatanavicharn, Jessica L. Waxler, Klaas J. Wierenga, Matthias T. F. Wolf, Sik-Nin Wong, Sebastian A. Leidel, Gessica Truglio, Peter C. Dedon, Annapurna Poduri, Shrikant Mane, Richard P. Lifton, Maxime Bouchard, Pekka Kannus, David Chitayat, Daniella Magen, Bert Callewaert, Herman van Tilbeurgh, Martin Zenker

    Foilsithe / Cruthaithe 2017
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