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Items: 13


Nondystrophic myotonia: challenges and future directions.

Trivedi JR, Cannon SC, Griggs RC.

Exp Neurol. 2014 Mar;253:28-30. doi: 10.1016/j.expneurol.2013.12.005. Epub 2013 Dec 18.


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.


Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channels.

Lee TT, Zhang XD, Chuang CC, Chen JJ, Chen YA, Chen SC, Chen TY, Tang CY.

PLoS One. 2013;8(2):e55930. doi: 10.1371/journal.pone.0055930. Epub 2013 Feb 12.


Physiology and pathophysiology of CLC-1: mechanisms of a chloride channel disease, myotonia.

Tang CY, Chen TY.

J Biomed Biotechnol. 2011;2011:685328. doi: 10.1155/2011/685328. Epub 2011 Dec 1. Review.


Skeletal muscle na channel disorders.

Simkin D, Bendahhou S.

Front Pharmacol. 2011 Oct 14;2:63. doi: 10.3389/fphar.2011.00063. eCollection 2011.


Impaired Wheel Running Exercise in CLC-1 Chloride Channel-Deficient Myotonic Mice.

van Lunteren E, Moyer M, Cooperrider J, Pollarine J.

Front Physiol. 2011 Aug 9;2:47. doi: 10.3389/fphys.2011.00047. eCollection 2011.


An interactive voice response diary for patients with non-dystrophic myotonia.

Statland JM, Wang Y, Richesson R, Bundy B, Herbelin L, Gomes J, Trivedi J, Venance S, Amato A, Hanna M, Griggs R, Barohn RJ; Cinch Consortium..

Muscle Nerve. 2011 Jul;44(1):30-5. doi: 10.1002/mus.22007.


Fatigue-inducing stimulation resolves myotonia in a drug-induced model.

van Lunteren E, Spiegler SE, Moyer M.

BMC Physiol. 2011 Feb 28;11:5. doi: 10.1186/1472-6793-11-5.


Warm-up phenomenon in myotonia associated with the V445M sodium channel mutation.

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

J Neurol. 2007 Feb;254(2):257-8. Epub 2007 Mar 2. No abstract available.


A novel syndrome of episodic muscle weakness maps to xp22.3.

Ryan MM, Taylor P, Donald JA, Ouvrier RA, Morgan G, Danta G, Buckley MF, North KN.

Am J Hum Genet. 1999 Oct;65(4):1104-13.


Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker).

Koch MC, Ricker K, Otto M, Wolf F, Zoll B, Lorenz C, Steinmeyer K, Jentsch TJ.

J Med Genet. 1993 Nov;30(11):914-7.



Howard RS.

BMJ. 1994 Aug 6;309(6951):392-5. Review. No abstract available.

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