Search Results

There are 5620 results for: content related to: Ca V 2.1 ablation in cortical interneurons selectively impairs fast-spiking basket cells and causes generalized seizures

  1. High cortical spreading depression susceptibility and migraine-associated symptoms in Cav2.1 S218L mice

    Annals of Neurology

    Volume 67, Issue 1, January 2010, Pages: 85–98, Arn M. J. M. van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E. Hoebeek, Curtis F. Barrett, Lisa Gherardini, Rob C. G. van de Ven, Boyan Todorov, Ludo A. M. Broos, Angelita Tottene, Zhenyu Gao, Mariann Fodor, Chris I. De Zeeuw, Rune R. Frants, Nikolaus Plesnila, Jaap J. Plomp, Daniela Pietrobon and Michel D. Ferrari

    Version of Record online : 4 AUG 2009, DOI: 10.1002/ana.21815

  2. You have free access to this content
    Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy

    The Journal of Physiology

    Volume 588, Issue 11, June 2010, Pages: 1905–1913, Sanjeev Rajakulendran, Tracey D. Graves, Robyn W. Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B. Davis, Rosalyn Davies, Nicholas W. Wood, Dimitri M. Kullmann, Michael G. Hanna and Stephanie Schorge

    Version of Record online : 28 MAY 2010, DOI: 10.1113/jphysiol.2009.186437

  3. You have free access to this content
    The P/Q channel in human disease: untangling the genetics and physiology

    Wiley Interdisciplinary Reviews: Membrane Transport and Signaling

    Volume 1, Issue 3, May/June 2012, Pages: 311–320, Stephanie Schorge and Sanjeev Rajakulendran

    Version of Record online : 23 JAN 2012, DOI: 10.1002/wmts.22

  4. You have full text access to this OnlineOpen article
    Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies

    Molecular Genetics & Genomic Medicine

    Volume 1, Issue 4, November 2013, Pages: 206–222, Oriel Carreño, Roser Corominas, Selma Angèlica Serra, Cèlia Sintas, Noèlia Fernández-Castillo, Marta Vila-Pueyo, Claudio Toma, Gemma G. Gené, Roser Pons, Miguel Llaneza, María-Jesús Sobrido, Daniel Grinberg, Miguel Ángel Valverde, José Manuel Fernández-Fernández, Alfons Macaya and Bru Cormand

    Version of Record online : 2 JUL 2013, DOI: 10.1002/mgg3.24

  5. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility

    American Journal of Medical Genetics

    Volume 105, Issue 8, 8 December 2001, Pages: 707–712, Rod A. Lea, Robert P. Curtain, Colin Hutchins, Peter J. Brimage and Lyn R. Griffiths

    Version of Record online : 30 OCT 2001, DOI: 10.1002/ajmg.1609

  6. Eye movement disorders are an early manifestation of CACNA1A mutations in children

    Developmental Medicine & Child Neurology

    Volume 58, Issue 6, June 2016, Pages: 639–644, Esther M Tantsis, Deepak Gill, Lyn Griffiths, Sachin Gupta, John Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert Smith, Christopher Troedson, Richard Webster and Manoj P Menezes

    Version of Record online : 27 JAN 2016, DOI: 10.1111/dmcn.13033

  7. Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes


    Volume 28, Issue 10, October 2008, Pages: 1039–1047, E Cuenca-León, R Corominas, N Fernàndez-Castillo, V Volpini, M Del Toro, M Roig, A Macaya and B Cormand

    Version of Record online : 17 JUL 2008, DOI: 10.1111/j.1468-2982.2008.01645.x

  8. You have free access to this content
    Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A

    Genes, Brain and Behavior

    Volume 6, Issue 8, November 2007, Pages: 717–727, G. Xie, S. J. Clapcote, B. J. Nieman, T. Tallerico, Y. Huang, I. Vukobradovic, S. P. Cordes, L. R. Osborne, J. Rossant, J. G. Sled, J. T. Henderson and J. C. Roder

    Version of Record online : 2 FEB 2007, DOI: 10.1111/j.1601-183X.2007.00302.x

  9. 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

  10. Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients


    Volume 28, Issue 9, September 2008, Pages: 914–921, LL Thomsen, E Oestergaard, A Bjornsson, H Stefansson, AC Fasquel, J Gulcher, K Stefansson and J Olesen

    Version of Record online : 30 MAY 2008, DOI: 10.1111/j.1468-2982.2008.01599.x

  11. Chromosome 19p13 loci in Finnish migraine with aura families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 132B, Issue 1, 5 January 2005, Pages: 85–89, Mari A. Kaunisto, Päivi J. Tikka, Mikko Kallela, Suzanne M. Leal, Jeanette C. Papp, Arja Korhonen, Eija Hämäläinen, Hanna Harno, Hannele Havanka, Markku Nissilä, Erkki Säkö, Matti Ilmavirta, Jaakko Kaprio, Markus Färkkilä, Roel A. Ophoff, Aarno Palotie and Maija Wessman

    Version of Record online : 24 SEP 2004, DOI: 10.1002/ajmg.b.30082

  12. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits

    Annals of Neurology

    Volume 54, Issue 6, December 2003, Pages: 725–731, S. H. Subramony, Kelly Schott, Robert S. Raike, Joel Callahan, Leigh R. Langford, Peka S. Christova, John H. Anderson and Christopher M. Gomez

    Version of Record online : 28 OCT 2003, DOI: 10.1002/ana.10756

  13. You have full text access to this OnlineOpen article
    Next-generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2

    Molecular Genetics & Genomic Medicine

    Volume 4, Issue 2, March 2016, Pages: 211–222, Neven Maksemous, Bishakha Roy, Robert A. Smith and Lyn R. Griffiths

    Version of Record online : 20 JAN 2016, DOI: 10.1002/mgg3.196

  14. Migrainous Vertigo: Mutation Analysis of the Candidate Genes CACNA1A, ATP1A2, SCN1A, and CACNB4

    Headache: The Journal of Head and Face Pain

    Volume 46, Issue 7, July/August 2006, Pages: 1136–1141, Michael Von Brevern, Nga Ta, Anupama Shankar, Anna Wiste, Anne Siegel, Andrea Radtke, Thomas Sander and Andrew Escayg

    Version of Record online : 6 JUL 2006, DOI: 10.1111/j.1526-4610.2006.00504.x

  15. You have free access to this content
    The voltage-gated calcium channel UNC-2 is involved in stress-mediated regulation of tryptophan hydroxylase

    Journal of Neurochemistry

    Volume 88, Issue 1, January 2004, Pages: 102–113, Miguel Estevez, Annette O. Estevez, Robin H. Cowie and Kathy L. Gardner

    Version of Record online : 28 NOV 2003, DOI: 10.1046/j.1471-4159.2003.02140.x

  16. Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation


    Volume 28, Issue 4, April 2008, Pages: 403–407, T Freilinger, M Bohe, B Wegener, B Müller-Myhsok, M Dichgans and H Knoblauch

    Version of Record online : 14 FEB 2008, DOI: 10.1111/j.1468-2982.2008.01540.x

  17. Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

    Annals of Neurology

    Volume 49, Issue 6, June 2001, Pages: 753–760, Esther E. Kors, Gisela M. Terwindt, Frans L.M.G. Vermeulen, Robin B. Fitzsimons, Philip E. Jardine, Peter Heywood, Seth Love, Arn M.J.M. Van Den Maagdenberg, Joost Haan, Rune R. Frants and Michel D. Ferrari

    Version of Record online : 2 APR 2001, DOI: 10.1002/ana.1031

  18. Invertebrate Modeling of a Migraine Channelopathy

    Headache: The Journal of Head and Face Pain

    Volume 46, Issue s1, June 2006, Pages: S25–S31, Miguel Estevez

    Version of Record online : 24 MAY 2006, DOI: 10.1111/j.1526-4610.2006.00487.x

  19. Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A

    Headache: The Journal of Head and Face Pain

    Volume 43, Issue 8, September 2003, Pages: 892–895, Kristine M. Chapman, Blazej I. Szczygielski, Cory Toth, Andrew Woolfenden, Gordon Robinson, Terrance P. Snutch and Siân D. Spacey

    Version of Record online : 27 AUG 2003, DOI: 10.1046/j.1526-4610.2003.03168.x

  20. Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation

    Headache: The Journal of Head and Face Pain

    Volume 51, Issue 10, November/December 2011, Pages: 1542–1546, Oriel Carreño, María Teresa García-Silva, Óscar García-Campos, Ana Martínez-de Aragón, Bru Cormand and Alfons Macaya

    Version of Record online : 14 NOV 2011, DOI: 10.1111/j.1526-4610.2011.02014.x