Literature DB >> 26943780

Rare neurological channelopathies--networks to study patients, pathogenesis and treatment.

Joanna C Jen1, Tetsuo Ashizawa2, Robert C Griggs3, Michael F Waters4.   

Abstract

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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Year:  2016        PMID: 26943780      PMCID: PMC6609097          DOI: 10.1038/nrneurol.2016.18

Source DB:  PubMed          Journal:  Nat Rev Neurol        ISSN: 1759-4758            Impact factor:   42.937


  64 in total

1.  Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

Authors:  J Julien; C Denier; X Ferrer; A Ducros; J Saintarailles; A Lagueny; E Tournier-Lasserve; C Vital
Journal:  J Neurol       Date:  2001-03       Impact factor: 4.849

2.  Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.

Authors:  Michael F Waters; Natali A Minassian; Giovanni Stevanin; Karla P Figueroa; John P A Bannister; Dagmar Nolte; Allan F Mock; Virgilio Gerald H Evidente; Dominic B Fee; Ulrich Müller; Alexandra Dürr; Alexis Brice; Diane M Papazian; Stefan M Pulst
Journal:  Nat Genet       Date:  2006-02-26       Impact factor: 38.330

3.  High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression.

Authors:  Yuting Shi; Chunrong Wang; Fengzhen Huang; Zhao Chen; Zhanfang Sun; Junling Wang; Beisha Tang; Tetsuo Ashizawa; Thomas Klockgether; Hong Jiang
Journal:  Cerebellum       Date:  2015-12       Impact factor: 3.847

4.  Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.

Authors:  Brent L Fogel; Hane Lee; Joshua L Deignan; Samuel P Strom; Sibel Kantarci; Xizhe Wang; Fabiola Quintero-Rivera; Eric Vilain; Wayne W Grody; Susan Perlman; Daniel H Geschwind; Stanley F Nelson
Journal:  JAMA Neurol       Date:  2014-10       Impact factor: 18.302

Review 5.  Primary episodic ataxias: diagnosis, pathogenesis and treatment.

Authors:  J C Jen; T D Graves; E J Hess; M G Hanna; R C Griggs; R W Baloh
Journal:  Brain       Date:  2007-06-15       Impact factor: 13.501

6.  A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.

Authors:  Yosuke Kokunai; Tomohiko Nakata; Mitsuru Furuta; Souhei Sakata; Hiromi Kimura; Takeshi Aiba; Masao Yoshinaga; Yusuke Osaki; Masayuki Nakamori; Hideki Itoh; Takako Sato; Tomoya Kubota; Kazushige Kadota; Katsuro Shindo; Hideki Mochizuki; Wataru Shimizu; Minoru Horie; Yasushi Okamura; Kinji Ohno; Masanori P Takahashi
Journal:  Neurology       Date:  2014-02-26       Impact factor: 9.910

Review 7.  Teleneurology applications: Report of the Telemedicine Work Group of the American Academy of Neurology.

Authors:  Lawrence R Wechsler; Jack W Tsao; Steven R Levine; Rebecca J Swain-Eng; Robert J Adams; Bart M Demaerschalk; David C Hess; Elena Moro; Lee H Schwamm; Steve Steffensen; Barney J Stern; Steven J Zuckerman; Pratik Bhattacharya; Larry E Davis; Ilana R Yurkiewicz; Aimee L Alphonso
Journal:  Neurology       Date:  2013-02-12       Impact factor: 9.910

8.  Clinical research for rare disease: opportunities, challenges, and solutions.

Authors:  Robert C Griggs; Mark Batshaw; Mary Dunkle; Rashmi Gopal-Srivastava; Edward Kaye; Jeffrey Krischer; Tan Nguyen; Kathleen Paulus; Peter A Merkel
Journal:  Mol Genet Metab       Date:  2008-11-13       Impact factor: 4.797

9.  Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.

Authors:  Sophie Tezenas du Montcel; Alexandra Durr; Peter Bauer; Karla P Figueroa; Yaeko Ichikawa; Alessandro Brussino; Sylvie Forlani; Maria Rakowicz; Ludger Schöls; Caterina Mariotti; Bart P C van de Warrenburg; Laura Orsi; Paola Giunti; Alessandro Filla; Sandra Szymanski; Thomas Klockgether; José Berciano; Massimo Pandolfo; Sylvia Boesch; Bela Melegh; Dagmar Timmann; Paola Mandich; Agnès Camuzat; Jun Goto; Tetsuo Ashizawa; Cécile Cazeneuve; Shoji Tsuji; Stefan-M Pulst; Alfredo Brusco; Olaf Riess; Alexis Brice; Giovanni Stevanin
Journal:  Brain       Date:  2014-06-26       Impact factor: 13.501

10.  Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.

Authors:  Joyce van de Leemput; Jayanth Chandran; Melanie A Knight; Lynne A Holtzclaw; Sonja Scholz; Mark R Cookson; Henry Houlden; Katrina Gwinn-Hardy; Hon-Chung Fung; Xian Lin; Dena Hernandez; Javier Simon-Sanchez; Nick W Wood; Paola Giunti; Ian Rafferty; John Hardy; Elsdon Storey; R J McKinlay Gardner; Susan M Forrest; Elizabeth M C Fisher; James T Russell; Huaibin Cai; Andrew B Singleton
Journal:  PLoS Genet       Date:  2007-05-16       Impact factor: 5.917

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  6 in total

Review 1.  Spinocerebellar ataxias: prospects and challenges for therapy development.

Authors:  Tetsuo Ashizawa; Gülin Öz; Henry L Paulson
Journal:  Nat Rev Neurol       Date:  2018-10       Impact factor: 42.937

2.  Protein surface topography as a tool to enhance the selective activity of a potassium channel blocker.

Authors:  Antonina A Berkut; Anton O Chugunov; Konstantin S Mineev; Steve Peigneur; Valentin M Tabakmakher; Nikolay A Krylov; Peter B Oparin; Alyona F Lihonosova; Ekaterina V Novikova; Alexander S Arseniev; Eugene V Grishin; Jan Tytgat; Roman G Efremov; Alexander A Vassilevski
Journal:  J Biol Chem       Date:  2019-09-18       Impact factor: 5.157

3.  Importance of an International Registry for and Collaborative Research on Esophageal Atresia.

Authors:  Frédéric Gottrand; Delphine Ley; Laurent Michaud; Rony Sfeir
Journal:  Front Pediatr       Date:  2017-04-20       Impact factor: 3.418

4.  Reduced Function of the Glutathione S-Transferase S1 Suppresses Behavioral Hyperexcitability in Drosophila Expressing Mutant Voltage-Gated Sodium Channels.

Authors:  Hung-Lin Chen; Junko Kasuya; Patrick Lansdon; Garrett Kaas; Hanxi Tang; Maggie Sodders; Toshihiro Kitamoto
Journal:  G3 (Bethesda)       Date:  2020-04-09       Impact factor: 3.154

5.  Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases.

Authors:  C Painous; N J H van Os; A Delamarre; I Michailoviene; M J Marti; B P van de Warrenburg; W G Meissner; A Utkus; C Reinhard; H Graessner; M A Tijssen
Journal:  Eur J Neurol       Date:  2020-06-19       Impact factor: 6.089

6.  Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies.

Authors:  Regina C Betz; Silke Redler; Evgeniya Denisova; Dana Westphal; Harald M Surowy; Friedegund Meier; Barbara Hutter; Julia Reifenberger; Arno Rütten; Alexander Schulz; Mildred Sergon; Mirjana Ziemer; Benedikt Brors
Journal:  Cancer Gene Ther       Date:  2021-05-27       Impact factor: 5.854

  6 in total

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