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Cited In for PubMed (Select 7980103)


Muscle channelopathies: the nondystrophic myotonias and periodic paralyses.

Statland JM, Barohn RJ.

Continuum (Minneap Minn). 2013 Dec;19(6 Muscle Disease):1598-614. doi: 10.1212/01.CON.0000440661.49298.c8. Review.


Non-dystrophic myotonia: prospective study of objective and patient reported outcomes.

Trivedi JR, Bundy B, Statland J, Salajegheh M, Rayan DR, Venance SL, Wang Y, Fialho D, Matthews E, Cleland J, Gorham N, Herbelin L, Cannon S, Amato A, Griggs RC, Hanna MG, Barohn RJ; CINCH Consortium.

Brain. 2013 Jul;136(Pt 7):2189-200. doi: 10.1093/brain/awt133. Epub 2013 Jun 13.


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

Statland JM, Bundy BN, Wang Y, Trivedi JR, Raja Rayan D, Herbelin L, Donlan M, McLin R, Eichinger KJ, Findlater K, Dewar L, Pandya S, Martens WB, Venance SL, Matthews E, Amato AA, Hanna MG, Griggs RC, Barohn RJ; CINCH Consortium.

Muscle Nerve. 2012 Oct;46(4):482-9. doi: 10.1002/mus.23402.


Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians.

Zhao J, Duprè N, Puymirat J, Chahine M.

J Physiol. 2012 Jun 1;590(Pt 11):2629-44. doi: 10.1113/jphysiol.2011.223461. Epub 2012 Jan 16.


Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorder.

Simkin D, Léna I, Landrieu P, Lion-François L, Sternberg D, Fontaine B, Bendahhou S.

J Physiol. 2011 Jul 1;589(Pt 13):3115-24. doi: 10.1113/jphysiol.2011.207977. Epub 2011 Apr 26.


Muscle channelopathies and electrophysiological approach.

Cherian A, Baheti NN, Kuruvilla A.

Ann Indian Acad Neurol. 2008 Jan;11(1):20-7. doi: 10.4103/0972-2327.40221.


The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Matthews E, Fialho D, Tan SV, Venance SL, Cannon SC, Sternberg D, Fontaine B, Amato AA, Barohn RJ, Griggs RC, Hanna MG; CINCH Investigators.

Brain. 2010 Jan;133(Pt 1):9-22. doi: 10.1093/brain/awp294. Epub 2009 Nov 16. Review.


Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss.

Mackenzie FE, Parker A, Parkinson NJ, Oliver PL, Brooker D, Underhill P, Lukashkina VA, Lukashkin AN, Holmes C, Brown SD.

Genes Brain Behav. 2009 Oct;8(7):699-713. doi: 10.1111/j.1601-183X.2009.00514.x. Epub 2009 Jun 22.


Diagnostics and therapy of muscle channelopathies--Guidelines of the Ulm Muscle Centre.

Lehmann-Horn F, Jurkat-Rott K, Rüdel R; Ulm Muscle Centre.

Acta Myol. 2008 Dec;27:98-113. Review.


Health status in non-dystrophic myotonias: close relation with pain and fatigue.

Trip J, de Vries J, Drost G, Ginjaar HB, van Engelen BG, Faber CG.

J Neurol. 2009 Jun;256(6):939-47. doi: 10.1007/s00415-009-5049-y. Epub 2009 Mar 1.


The dominant cold-sensitive Out-cold mutants of Drosophila melanogaster have novel missense mutations in the voltage-gated sodium channel gene paralytic.

Lindsay HA, Baines R, ffrench-Constant R, Lilley K, Jacobs HT, O'Dell KM.

Genetics. 2008 Oct;180(2):873-84. doi: 10.1534/genetics.108.090951. Epub 2008 Aug 24.


Practical aspects in the management of hypokalemic periodic paralysis.

Levitt JO.

J Transl Med. 2008 Apr 21;6:18. doi: 10.1186/1479-5876-6-18. Erratum in: J Transl Med. 2014;12:198. Dosage error in article text.


Muscle channelopathies and critical points in functional and genetic studies.

Jurkat-Rott K, Lehmann-Horn F.

J Clin Invest. 2005 Aug;115(8):2000-9. Review.


Inherited disorders of voltage-gated sodium channels.

George AL Jr.

J Clin Invest. 2005 Aug;115(8):1990-9. Review.


Neurological channelopathies.

Graves TD, Hanna MG.

Postgrad Med J. 2005 Jan;81(951):20-32. Review.


Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.

Kim J, Hahn Y, Sohn EH, Lee YJ, Yun JH, Kim JM, Chung JH.

J Neurol Neurosurg Psychiatry. 2001 May;70(5):618-23.


Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker.

Hayward LJ, Brown RH Jr, Cannon SC.

J Gen Physiol. 1996 May;107(5):559-76.

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