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Items: 1 to 20 of 33

1.

Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians.

Dupré N, Chrestian N, Bouchard JP, Rossignol E, Brunet D, Sternberg D, Brais B, Mathieu J, Puymirat J.

Neuromuscul Disord. 2009 May;19(5):330-4. doi: 10.1016/j.nmd.2008.01.007. Epub 2008 Mar 11.

PMID:
18337100
2.

The skeletal muscle sodium and chloride channel diseases.

Hudson AJ, Ebers GC, Bulman DE.

Brain. 1995 Apr;118 ( Pt 2):547-63. Review.

PMID:
7735894
3.

Treatment in myotonia and periodic paralysis.

Meola G, Sansone V.

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

PMID:
15269662
4.

Phenotypic variability in myotonia congenita.

Colding-Jørgensen E.

Muscle Nerve. 2005 Jul;32(1):19-34. Review.

PMID:
15786415
5.

Myotonia caused by mutations in the muscle chloride channel gene CLCN1.

Pusch M.

Hum Mutat. 2002 Apr;19(4):423-34. Review.

PMID:
11933197
6.

The myotonias: their diagnosis and treatment.

Moxley RT 3rd.

Compr Ther. 1996 Jan;22(1):8-21. Review. No abstract available.

PMID:
8654027
7.

Myotonia congenita.

Lossin C, George AL Jr.

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

PMID:
19185184
8.

Sodium channel defects in myotonia and periodic paralysis.

Cannon SC.

Annu Rev Neurosci. 1996;19:141-64. Review.

PMID:
8833439
9.

Myotonias due to CLC-1 chloride channel mutations.

Jentsch TJ, Lorenz C, Pusch M, Steinmeyer K.

Soc Gen Physiol Ser. 1995;50:149-59. Review. No abstract available.

PMID:
7676320
10.

Therapy in myotonic disorders and in muscle channelopathies.

Meola G, Sansone V.

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

11.

The diagnosis and treatment of myotonic disorders.

Heatwole CR, Statland JM, Logigian EL.

Muscle Nerve. 2013 May;47(5):632-48. doi: 10.1002/mus.23683. Epub 2013 Mar 27. Review.

PMID:
23536309
12.

Myotonic disorders.

Mankodi A.

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

13.

Channelopathies: the nondystrophic myotonias and periodic paralyses.

Lehmann-Horn F, Rüdel R.

Semin Pediatr Neurol. 1996 Jun;3(2):122-39. Review.

PMID:
8795846
14.

Quantitative myotonia assessment: an experimental protocol.

Sansone V, Marinou K, Salvucci J, Meola G.

Neurol Sci. 2000;21(5 Suppl):S971-4. Review.

16.

A clinical approach to muscle diseases.

Jackson CE.

Semin Neurol. 2008 Apr;28(2):228-40. doi: 10.1055/s-2008-1062266. Review.

PMID:
18351524
17.

Skeletal muscle channelopathies.

Jurkat-Rott K, Lerche H, Lehmann-Horn F.

J Neurol. 2002 Nov;249(11):1493-502. Review.

PMID:
12420087
18.

[Muscle weakness or rigidity due to hereditary ion channel diseases].

Links TP, van der Hoeven JH.

Ned Tijdschr Geneeskd. 2001 Feb 10;145(6):249-51. Review. Dutch.

PMID:
11236369
19.

[Electrophysiological testing in muscle channelopathies].

Kuntzer T.

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

PMID:
15269661
20.

Myotonic disorders and periodic paralysis.

Carey N, Johnson KJ.

Baillieres Clin Neurol. 1994 Aug;3(2):387-405. Review.

PMID:
7952854

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