ENHANCEMENTS TO THE RARE DISEASES CLINICAL RESEARCH NETWORK CONTACT REGISTRY FOR THE INHERITED NEUROPATHIES CONSORTIUM

被引：0
|
作者：
Marking, D. [1 ]
Shy, M. [2 ]
机构：
[1] Univ S Florida, Tampa, FL USA
[2] Univ Iowa Hlth Care, Iowa City, IA USA
来源：
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM | 2017年 / 22卷 / 03期
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：337 / 338
页数：2
相关论文
共 50 条
  • [41] Treatment of chronic immune-mediated neuropathies: Impact of the Rare Diseases Centers network in Italy
    Nobile-Orazio, E.
    [J]. REVUE NEUROLOGIQUE, 2013, 169 : S33 - S38
  • [42] Establishment of a registry of clinical data and bioresources for rare nervous system diseases
    Kim, Dayoung
    Kim, Sooyoung
    Seok, Jin Myoung
    Shin, Kyong Jin
    Oh, Eungseok
    Jeon, Mi Young
    Park, Joungkyu
    Chang, Hee Jin
    Youn, Jinyoung
    Oh, Jeeyoung
    Sohn, Eunhee
    Park, Jinse
    Cho, Jin Whan
    Kim, Byoung Joon
    [J]. OSONG PUBLIC HEALTH AND RESEARCH PERSPECTIVES, 2024, 15 (02) : 174 - 181
  • [43] CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network
    Relling, M. V.
    Klein, T. E.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2011, 89 (03) : 464 - 467
  • [44] Dominantly Inherited Alzheimer Network: facilitating research and clinical trials
    Krista L Moulder
    B Joy Snider
    Susan L Mills
    Virginia D Buckles
    Anna M Santacruz
    Randall J Bateman
    John C Morris
    [J]. Alzheimer's Research & Therapy, 5
  • [45] Dominantly Inherited Alzheimer Network: facilitating research and clinical trials
    Moulder, Krista L.
    Snider, B. Joy
    Mills, Susan L.
    Buckles, Virginia D.
    Santacruz, Anna M.
    Bateman, Randall J.
    Morris, John C.
    [J]. ALZHEIMERS RESEARCH & THERAPY, 2013, 5 (05)
  • [46] Rare disease clinical research network's urea cycle consortium delivers a successful clinical trial to improve alternate pathway therapy
    Mistry, Pramod K.
    [J]. HEPATOLOGY, 2013, 57 (06) : 2100 - 2102
  • [47] Clinical research challenges in rare genetic diseases in Brazil
    Giugliani, Luciana
    Vanzella, Claudia
    Zambrano, Marina Bauer
    Donis, Karina Carvalho
    Wendland Wallau, Thais Klassmann
    da Costa, Fernando Machado
    Giugliani, Roberto
    [J]. GENETICS AND MOLECULAR BIOLOGY, 2019, 42 (01) : 305 - 311
  • [48] Clinical and genetic characterization of patients with eye diseases included in the Spanish Rare Diseases Patient Registry
    Lopez-de la Rosa, Alberto
    Telleria, Juan J.
    de la Paz, Manuel Posada
    Hermosilla-Gimeno, Isabel M.
    Rivas, Miren Agurtzane
    Gilabert, Raul
    Coco-Martin, Rosa M.
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2024, 19 (01)
  • [49] Methodological issues relevant to clinical research in rare diseases
    Dib, M
    Meininger, V
    Boissel, JP
    [J]. REVUE NEUROLOGIQUE, 2003, 159 (6-7) : 703 - 708
  • [50] Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network
    Kylie Tingley
    Monica Lamoureux
    Michael Pugliese
    Michael T. Geraghty
    Jonathan B. Kronick
    Beth K. Potter
    Doug Coyle
    Kumanan Wilson
    Michael Kowalski
    Valerie Austin
    Catherine Brunel-Guitton
    Daniela Buhas
    Alicia K. J. Chan
    Sarah Dyack
    Annette Feigenbaum
    Alette Giezen
    Sharan Goobie
    Cheryl R. Greenberg
    Shailly Jain Ghai
    Michal Inbar-Feigenberg
    Natalya Karp
    Mariya Kozenko
    Erica Langley
    Matthew Lines
    Julian Little
    Jennifer MacKenzie
    Bruno Maranda
    Saadet Mercimek-Andrews
    Connie Mohan
    Aizeddin Mhanni
    Grant Mitchell
    John J. Mitchell
    Laura Nagy
    Melanie Napier
    Amy Pender
    Murray Potter
    Chitra Prasad
    Suzanne Ratko
    Ramona Salvarinova
    Andreas Schulze
    Komudi Siriwardena
    Neal Sondheimer
    Rebecca Sparkes
    Sylvia Stockler-Ipsiroglu
    Yannis Trakadis
    Lesley Turner
    Clara Van Karnebeek
    Hilary Vallance
    Anthony Vandersteen
    Jagdeep Walia
    [J]. Orphanet Journal of Rare Diseases, 15
12345