TY - JOUR
T1 - Rare neurological channelopathies-networks to study patients, pathogenesis and treatment
AU - Jen, Joanna C.
AU - Ashizawa, Tetsuo
AU - Griggs, Robert C.
AU - Waters, Michael F.
N1 - Funding Information:
The CINCH and CRC-SCA consortia were participants of the Rare Disease Clinical Research Network supported by the Office of Rare Disease Research and the National Center for Advancing Translational Sciences of the NIH. Both consortia were supported by the National Institute of Neurological Disorders and Stroke. CINCH received support from the Muscular Dystrophy Association. CRC-SCA received support from the National Ataxia Foundation.
Publisher Copyright:
© 2016 Macmillan Publishers Limited. All rights reserved.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Each of the thousands of rare neurological diseases requires a widely distributed network of centres, investigators and patients, so as to foster multidisciplinary investigations and involve sufficient numbers of patients in the discovery of disease pathogenesis and novel treatment. In this Review, we highlight the value of this collaborative approach in patient-oriented research into rare neurological channelopathies. Two networks, the Consortium for Clinical Investigations of Neurological Channelopathies (CINCH) and the Clinical Research Consortium for Studies of Cerebellar Ataxias (CRC-SCA), provide a link between patients with rare channelopathies and investigators who are studying disease pathogenesis and developing novel treatments. Interactions between patients, researchers and advocacy groups promote shared agendas that benefit patient education and recruitment, research collaboration and funding, and training and mentoring of junior investigators who are attracted to the study of the diseases that provide the focus for the two networks. Here, we discuss how linkage of national and international centres has enabled recruitment of study participants, provided opportunities for novel studies of pathogenesis, and facilitated successful clinical trials.
AB - Each of the thousands of rare neurological diseases requires a widely distributed network of centres, investigators and patients, so as to foster multidisciplinary investigations and involve sufficient numbers of patients in the discovery of disease pathogenesis and novel treatment. In this Review, we highlight the value of this collaborative approach in patient-oriented research into rare neurological channelopathies. Two networks, the Consortium for Clinical Investigations of Neurological Channelopathies (CINCH) and the Clinical Research Consortium for Studies of Cerebellar Ataxias (CRC-SCA), provide a link between patients with rare channelopathies and investigators who are studying disease pathogenesis and developing novel treatments. Interactions between patients, researchers and advocacy groups promote shared agendas that benefit patient education and recruitment, research collaboration and funding, and training and mentoring of junior investigators who are attracted to the study of the diseases that provide the focus for the two networks. Here, we discuss how linkage of national and international centres has enabled recruitment of study participants, provided opportunities for novel studies of pathogenesis, and facilitated successful clinical trials.
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U2 - 10.1038/nrneurol.2016.18
DO - 10.1038/nrneurol.2016.18
M3 - Review article
C2 - 26943780
AN - SCOPUS:84960158096
VL - 12
SP - 195
EP - 203
JO - Nature Reviews Neurology
JF - Nature Reviews Neurology
SN - 1759-4758
IS - 4
ER -