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Items: 1 to 20 of 22

1.

Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1.

Lueck JD, Lungu C, Mankodi A, Osborne RJ, Welle SL, Dirksen RT, Thornton CA.

Am J Physiol Cell Physiol. 2007 Apr;292(4):C1291-7. Epub 2006 Nov 29.

2.

RNA pathogenesis of the myotonic dystrophies.

Day JW, Ranum LP.

Neuromuscul Disord. 2005 Jan;15(1):5-16. Epub 2004 Nov 26. Review.

PMID:
15639115
3.

[Myotonic dystrophy].

Ishiura S, Oana K, Koebis M.

Rinsho Shinkeigaku. 2013;53(11):1109-11. Review. Japanese.

PMID:
24291894
4.

Myotonic disorders.

Mankodi A.

Neurol India. 2008 Jul-Sep;56(3):298-304. Review.

5.

[Myotonia and cardiac conduction defects in myotonic dystrophy and defect in ion channels].

Kubota T, Nakamori M, Takahashi MP.

Rinsho Byori. 2014 Mar;62(3):246-54. Review. Japanese.

PMID:
24800500
6.

Therapy in myotonic disorders and in muscle channelopathies.

Meola G, Sansone V.

Neurol Sci. 2000;21(5 Suppl):S953-61. Review.

PMID:
11382195
7.

Treatment in myotonia and periodic paralysis.

Meola G, Sansone V.

Rev Neurol (Paris). 2004 May;160(5 Pt 2):S55-69. Review.

PMID:
15269662
8.

Myogenic defects in myotonic dystrophy.

Amack JD, Mahadevan MS.

Dev Biol. 2004 Jan 15;265(2):294-301. Review.

9.

[Myotonia and channelopathy].

Kurihara T.

Rinsho Shinkeigaku. 1999 Dec;39(12):1219-21. Review. Japanese.

PMID:
10791081
10.

[Electrophysiological testing in muscle channelopathies].

Kuntzer T.

Rev Neurol (Paris). 2004 May;160(5 Pt 2):S49-54. Review. French.

PMID:
15269661
11.

Myotonia congenita.

Lossin C, George AL Jr.

Adv Genet. 2008;63:25-55. doi: 10.1016/S0065-2660(08)01002-X. Review.

PMID:
19185184
12.

Myotonic dystrophy 1 in the nervous system: from the clinic to molecular mechanisms.

de León MB, Cisneros B.

J Neurosci Res. 2008 Jan;86(1):18-26. Review.

PMID:
17549748
13.

Cerebral involvement in myotonic dystrophies.

Meola G, Sansone V.

Muscle Nerve. 2007 Sep;36(3):294-306. Review.

PMID:
17486579
14.

[Spontaneous electromyographic activity. Practical importance].

Georgesco M, Salerno A.

Neurophysiol Clin. 2000 Oct;30(5):289-305. Review. French.

PMID:
11126641
15.

Therapeutic approaches to ion channel diseases.

Camerino DC, Desaphy JF, Tricarico D, Pierno S, Liantonio A.

Adv Genet. 2008;64:81-145. doi: 10.1016/S0065-2660(08)00804-3. Review.

PMID:
19161833
16.

Structure and function of CLCA proteins.

Loewen ME, Forsyth GW.

Physiol Rev. 2005 Jul;85(3):1061-92. Review.

17.

Treatment of neuromuscular channelopathies: current concepts and future prospects.

Cleland JC, Griggs RC.

Neurotherapeutics. 2008 Oct;5(4):607-12. doi: 10.1016/j.nurt.2008.09.001. Review.

18.

[The spectrum of hereditary skeletal-muscle channelopathies].

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

Ned Tijdschr Geneeskd. 2005 Sep 17;149(38):2093-8. Review. Dutch.

PMID:
16201598
19.

[Myotonic disorder and channelopathy].

Kurihara T.

Nihon Naika Gakkai Zasshi. 2004 Mar 10;93(3):510-4. Review. Japanese. No abstract available.

PMID:
15052812
20.

Pain as a channelopathy.

Raouf R, Quick K, Wood JN.

J Clin Invest. 2010 Nov;120(11):3745-52. doi: 10.1172/JCI43158. Epub 2010 Nov 1. Review.

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