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There are 3327398 results for: content related to: Clinical features of a large Australian pedigree with episodic ataxia type 1

  1. You have free access to this content
    The Clinical Spectrum of Autosomal-Dominant Episodic Ataxias

    Movement Disorders Clinical Practice

    Volume 1, Issue 4, December 2014, Pages: 285–290, Stefan Kipfer and Michael Strupp

    Version of Record online : 28 JUL 2014, DOI: 10.1002/mdc3.12075

  2. Autosomal dominant episodic ataxia: A heterogeneous syndrome

    Movement Disorders

    Volume 1, Issue 4, 1986, Pages: 239–253, Dr. Stephen T. Gancher and John G. Nutt

    Version of Record online : 23 MAY 2005, DOI: 10.1002/mds.870010404

  3. Abstracts of The Movement Disorder Society's Twelfth International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 23, Issue S1, 15 May 2008, Pages: S1–S422,

    Version of Record online : 28 MAY 2008, DOI: 10.1002/mds.22133

  4. Ion channels and epilepsy

    American Journal of Medical Genetics

    Volume 106, Issue 2, Summer 2001, Pages: 146–159, Holger Lerche, Karin Jurkat-Rott and Frank Lehmann-Horn

    Version of Record online : 20 SEP 2001, DOI: 10.1002/ajmg.1582

  5. You have free access to this content
    Abstracts of The Movement Disorder Society's Eleventh International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 22, Issue S16, 2007, Pages: S1–S325,

    Version of Record online : 24 APR 2007, DOI: 10.1002/mds.21535

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    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

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    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  8. A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction

    Movement Disorders

    Volume 24, Issue 5, 15 April 2009, Pages: 778–782, Michelle K. Demos, Vincenzo Macri, Kevin Farrell, Tanya N. Nelson, Kristine Chapman, Eric Accili and Linlea Armstrong

    Version of Record online : 9 FEB 2009, DOI: 10.1002/mds.22467

  9. Familial dyskinesia and facial myokymia

    Movement Disorders

    Volume 17, Issue 4, July/August 2002, Page: 747, Thomas D. Bird

    Version of Record online : 17 MAY 2002, DOI: 10.1002/mds.10213

  10. Familial dyskinesia and facial myokymia (FDFM): A novel movement disorder

    Annals of Neurology

    Volume 49, Issue 4, April 2001, Pages: 486–492, Magali Fernandez, Wendy Raskind, John Wolff, Mark Matsushita, Eric Yuen, William Graf, Hillary Lipe and Thomas Bird

    Version of Record online : 2 APR 2001, DOI: 10.1002/ana.98

  11. Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p

    Annals of Neurology

    Volume 41, Issue 1, January 1997, Pages: 8–16, Dr Robert W. Baloh, Qing Yue, Joseph M. Furman and Stanley F. Nelson

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410410105

  12. Episodic ataxias as channelopathies

    Annals of Neurology

    Volume 37, Issue 3, March 1995, Pages: 285–287, Robert C. Griggs and John G. Nutt

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410370302

  13. Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea

    Muscle & Nerve

    Volume 37, Issue 3, March 2008, Pages: 399–402, Steven J. Shook, Hafsa Mamsa, Joanna C. Jen, Robert W. Baloh and Lan Zhou

    Version of Record online : 2 OCT 2007, DOI: 10.1002/mus.20904

  14. Genetic disorders of neuromuscular ion channels

    Muscle & Nerve

    Volume 26, Issue 3, September 2002, Pages: 299–325, Kleopas A. Kleopa and Robert L. Barchi

    Version of Record online : 5 JUN 2002, DOI: 10.1002/mus.10164

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    Episodic ataxia type 1 without episodic ataxia: the diagnostic utility of nerve excitability studies in individuals with KCNA1 mutations

    Developmental Medicine & Child Neurology

    Volume 55, Issue 10, October 2013, Pages: 959–962, S Veronica Tan, Elizabeth Wraige, Karine Lascelles and Hugh Bostock

    Version of Record online : 5 AUG 2013, DOI: 10.1111/dmcn.12236

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    A novel mutation in KCNA1 causes episodic ataxia without myokymia

    Human Mutation

    Volume 24, Issue 6, December 2004, Page: 536, Hane Lee, Hui Wang, Joanna C. Jen, Chiara Sabatti, Robert W. Baloh and Stanley F. Nelson

    Version of Record online : 5 NOV 2004, DOI: 10.1002/humu.9295

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    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Version of Record online : 6 JUN 2014, DOI: 10.1002/mds.25914

  18. Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

    Annals of Neurology

    Volume 48, Issue 4, October 2000, Pages: 647–656, L. H. Eunson, R. Rea, S. M. Zuberi, S. Youroukos, C. P. Panayiotopoulos, R. Liguori, P. Avoni, R. C. McWilliam, J. B. P. Stephenson, M. G. Hanna, D. M. Kullmann and A. Spauschus

    Version of Record online : 13 APR 2001, DOI: 10.1002/1531-8249(200010)48:4<647::AID-ANA12>3.0.CO;2-Q

  19. Eyelid myokymia in patients with migraine taking topiramate

    Acta Neurologica Scandinavica

    Volume 132, Issue 2, August 2015, Pages: 143–146, V. Medrano-Martínez, A. Pérez-Sempere, J. M. Moltó-Jordá, S. Fernández-Izquierdo, I. Francés-Pont, J. Mallada-Frechin and L. Piqueras-Rodríguez

    Version of Record online : 31 MAR 2015, DOI: 10.1111/ane.12395

  20. Familial Episodic Ataxia

    Annals of the New York Academy of Sciences

    Volume 1164, Issue 1, May 2009, Pages: 252–256, Joanna C. Jen and Robert W. Baloh

    Version of Record online : 21 MAY 2009, DOI: 10.1111/j.1749-6632.2008.03723.x