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There are 17837 results for: content related to: Refined exercise testing can aid dna-based diagnosis in muscle channelopathies

  1. Cortical involvement during myotonia in myotonic dystrophy: an fMRI study

    Acta Neurologica Scandinavica

    Volume 132, Issue 1, July 2015, Pages: 65–72, A. Toth, E. Lovadi, S. Komoly, A. Schwarcz, G. Orsi, G. Perlaki, P. Bogner, A. Sebok, N. Kovacs, E. Pal and J. Janszky

    Version of Record online : 28 JAN 2015, DOI: 10.1111/ane.12360

  2. AAEE minimonograph #27: Differential diagnosis of myotonic syndromes

    Muscle & Nerve

    Volume 10, Issue 7, September 1987, Pages: 603–615, Erich W. Streib

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880100704

  3. Myotonic Dystrophy and its Differential Diagnosis

    Acta Neurologica Scandinavica

    Volume 49, Issue s55, December 1973, Pages: 1–28, H. Zellweger and V. Ionasescu

    Version of Record online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1973.tb07597.x

  4. Hereditary myotonia in the Chow Chow

    Journal of Small Animal Practice

    Volume 22, Issue 7, July 1981, Pages: 451–465, B. R. H. FARROW and R. MALIK

    Version of Record online : 10 APR 2008, DOI: 10.1111/j.1748-5827.1981.tb00629.x


    Acta Neurologica Scandinavica

    Volume 39, Issue 1, March 1963, Pages: 41–58, Ingrid Gamstorp

    Version of Record online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1963.tb05386.x

  6. A quantitative measure of handgrip myotonia in non-dystrophic myotonia

    Muscle & Nerve

    Volume 46, Issue 4, October 2012, Pages: 482–489, Jeffrey M. Statland, Brian N. Bundy, Yunxia Wang, Jaya R. Trivedi, Dipa Raja Rayan, Laura Herbelin, Merideth Donlan, Rhonda McLin, Katy J. Eichinger, Karen Findlater, Liz Dewar, Shree Pandya, William B. Martens, Shannon L. Venance, Emma Matthews, Anthony A. Amato, Michael G. Hanna, Robert C. Griggs, Richard J. Barohn and and the CINCH Consortium

    Version of Record online : 13 SEP 2012, DOI: 10.1002/mus.23402

  7. The autosomal recessive (Becker) form of myotonia congenita

    Muscle & Nerve

    Volume 2, Issue 2, March/April 1979, Pages: 109–117, Dr S. Erich Kuhn, Dr. Walter Fiehn, Dr. Dieter Seiler and Dr. Joachim-Michael SchröDer

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880020205

  8. Clinical study of paramyotonia congenita with and without myotonia in a warm environment

    Muscle & Nerve

    Volume 4, Issue 5, September/October 1981, Pages: 388–395, Dr. Anton Haass, Dr. Kenneth Ricker, Dr. Reinhardt Rüdel, Dr. Frank Lehmann-Horn, Dr. Reinhard Böhlen, Dr. Reinhard Dengler and Dr. Hans Georg Mertens

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880040507

  9. Sodium channel slow inactivation as a therapeutic target for myotonia congenita

    Annals of Neurology

    Volume 77, Issue 2, February 2015, Pages: 320–332, Kevin R. Novak, Jennifer Norman, Jacob R. Mitchell, Martin J. Pinter and Mark M. Rich

    Version of Record online : 9 JAN 2015, DOI: 10.1002/ana.24331

  10. Myotonia in the rat diaphragm preparation caused by the sulfhydryl inhibiting para-substituted mercuribenzoates

    Acta Physiologica Scandinavica

    Volume 115, Issue 1, May 1982, Pages: 31–38, ASBJÖRN RÖED

    Version of Record online : 8 DEC 2008, DOI: 10.1111/j.1748-1716.1982.tb07042.x

  11. Effects of acetazolamide on myotonia

    Annals of Neurology

    Volume 3, Issue 6, June 1978, Pages: 531–537, Dr. Robert C. Griggs, Richard T. Moxley III, Jack E. Riggs and W. King Engel

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410030614


    Annals of Human Genetics

    Volume 21, Issue 4, May 1957, Pages: 318–351, MARGARET A LYNAS

    Version of Record online : 16 MAY 2014, DOI: 10.1111/j.1469-1809.1972.tb00203.x

  13. A congenital form of myotonia with dystrophic changes in a Quarterhorse

    Equine Veterinary Journal

    Volume 19, Issue 4, July 1987, Pages: 353–358, J. M. JAMISON, J. D. BAIRD, L. L. SMITH-MAXIE and T. J. HULLAND

    Version of Record online : 23 APR 2010, DOI: 10.1111/j.2042-3306.1987.tb01433.x

  14. The dominant chloride channel mutant G200R causing fluctuating myotonia: Clinical findings, electrophysiology, and channel pathology

    Muscle & Nerve

    Volume 21, Issue 9, September 1998, Pages: 1122–1128, Susanne Wagner, Feza Deymeer, Lothar L. Kürz, Sandra Benz, Lothar Schleithoff, Frank Lehmann-Horn, Piraye Serdaroğlu, Coskun Özdemir and Reinhardt Rüdel

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199809)21:9<1122::AID-MUS2>3.0.CO;2-9

  15. Aerobic training in myotonia congenita: Effect on myotonia and fitness

    Muscle & Nerve

    Accepted manuscript online: 31 DEC 2016, Grete Andersen, Nicoline Løkken and John Vissing

    DOI: 10.1002/mus.25549

  16. Myotonia and neuromuscular transmission in the mouse

    Muscle & Nerve

    Volume 14, Issue 8, August 1991, Pages: 775–780, MS Dirk Költgen, Dr., PhD Heinrich Brinkmeier and PhD Harald Jockusch

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880140813

  17. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

    Clinical Genetics

    Volume 80, Issue 6, December 2011, Pages: 574–580, C Sun, M Van Ghelue, L Tranebjærg, F Thyssen, Ø Nilssen and T Torbergsen

    Version of Record online : 19 JAN 2011, DOI: 10.1111/j.1399-0004.2010.01616.x

  18. You have full text access to this Open Access content
    A Novel Mutation of the CLCN1 Gene Associated with Myotonia Hereditaria in an Australian Cattle Dog

    Journal of Veterinary Internal Medicine

    Volume 21, Issue 3, May 2007, Pages: 458–463, Daniel F. Finnigan, W.J. Brad Hanna, Roberto Poma and Andrew J. Bendall

    Version of Record online : 5 FEB 2008, DOI: 10.1111/j.1939-1676.2007.tb02990.x

  19. The influence of skeletal muscle reinnervation on experimentally induced myotonia

    Muscle & Nerve

    Volume 9, Issue 4, May 1986, Pages: 364–366, Dr. Abdulsalam Al-sulaiman, Saad Al-Rajeh and Vasudeva Iyer

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880090414

  20. Severe neonatal non-dystrophic myotonia secondary to a novel mutation of the voltage-gated sodium channel (SCN4A) gene

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 3, 1 February 2008, Pages: 380–383, Sébastien Gay, Delphine Dupuis, Laurence Faivre, Alice Masurel-Paulet, Marc Labenne, Marina Colombani, Pierre Soichot, Frédéric Huet, Bernard Hainque, Damien Sternberg, Bertrand Fontaine, Jean-Bernard Gouyon and Christel Thauvin-Robinet

    Version of Record online : 17 JAN 2008, DOI: 10.1002/ajmg.a.32141