These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 17654559)

  • 1. Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.
    Michel P; Sternberg D; Jeannet PY; Dunand M; Thonney F; Kress W; Fontaine B; Fournier E; Kuntzer T
    Muscle Nerve; 2007 Nov; 36(5):643-50. PubMed ID: 17654559
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Decrement of compound muscle action potential is related to mutation type in myotonia congenita.
    Colding-Jørgensen E; DunØ M; Schwartz M; Vissing J
    Muscle Nerve; 2003 Apr; 27(4):449-55. PubMed ID: 12661046
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Muscle membrane polarisation after provocative tests, and after cooling: the normal CMAP changes to be expected.
    Kuntzer T; Michel P
    Clin Neurophysiol; 2004 Jun; 115(6):1457-63. PubMed ID: 15134715
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Reduced muscle-fiber conduction but normal slowing after cold exposure in paramyotonia congenita.
    Blijham PJ; Drost G; Stegeman DF; Zwarts MJ
    Muscle Nerve; 2008 Jan; 37(1):23-6. PubMed ID: 17823953
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Activity-induced weakness in recessive myotonia congenita with a novel (696+1G>A) mutation.
    McKay OM; Krishnan AV; Davis M; Kiernan MC
    Clin Neurophysiol; 2006 Sep; 117(9):2064-8. PubMed ID: 16854622
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Value of short exercise and short exercise with cooling tests in the diagnosis of myotonic dystrophies (DM1 and DM2).
    Gawel M; Szmidt-Salkowska E; Lusakowska A; Nojszewska M; Sulek A; Krysa W; Rajkiewicz M; Seroka A; Kaminska AM
    Muscle Nerve; 2014 Feb; 49(2):277-83. PubMed ID: 23716346
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neuromuscular excitability properties in myotonic dystrophy type 1.
    Boërio D; Hogrel JY; Bassez G; Lefaucheur JP
    Clin Neurophysiol; 2007 Nov; 118(11):2375-82. PubMed ID: 17890147
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 18337100
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
    Sun C; Van Ghelue M; Tranebjærg L; Thyssen F; Nilssen Ø; Torbergsen T
    Clin Genet; 2011 Dec; 80(6):574-80. PubMed ID: 21204798
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenita.
    Modoni A; D'Amico A; Dallapiccola B; Mereu ML; Merlini L; Pagliarani S; Pisaneschi E; Silvestri G; Torrente I; Valente EM; Lo Monaco M
    J Clin Neurophysiol; 2011 Feb; 28(1):39-44. PubMed ID: 21221019
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of paramyotonia congenita without periodic paralysis: electrophysiological and molecular genetic studies.
    Park JH; Lee YW; Park SA; Lee TK; Rho HJ; Sung KB
    Neurologist; 2010 May; 16(3):203-5. PubMed ID: 20445432
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.
    Logigian EL; Ciafaloni E; Quinn LC; Dilek N; Pandya S; Moxley RT; Thornton CA
    Muscle Nerve; 2007 Apr; 35(4):479-85. PubMed ID: 17230537
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cold extends electromyography distinction between ion channel mutations causing myotonia.
    Fournier E; Viala K; Gervais H; Sternberg D; Arzel-Hézode M; Laforêt P; Eymard B; Tabti N; Willer JC; Vial C; Fontaine B
    Ann Neurol; 2006 Sep; 60(3):356-65. PubMed ID: 16786525
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relief from episodic weakness with pyridostigmine in paramyotonia congenita: a family study.
    Khadilkar SV; Singh RK; Mansukhani KA; Urtizberea JA; Sternberg D
    Muscle Nerve; 2010 Jan; 41(1):133-7. PubMed ID: 19768756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distinguishing paramyotonia congenita and myotonia congenita by electromyography.
    Subramony SH; Malhotra CP; Mishra SK
    Muscle Nerve; 1983 Jun; 6(5):374-9. PubMed ID: 6888415
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification.
    Ferriby D; Stojkovic T; Sternberg D; Hurtevent JF; Hurtevent JP; Vermersch P
    Neuromuscul Disord; 2006 May; 16(5):321-4. PubMed ID: 16624558
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Axonal function and activity-dependent excitability changes in myotonic dystrophy.
    Krishnan AV; Kiernan MC
    Muscle Nerve; 2006 May; 33(5):627-36. PubMed ID: 16453325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New mutation of the Na channel in the severe form of potassium-aggravated myotonia.
    Kubota T; Kinoshita M; Sasaki R; Aoike F; Takahashi MP; Sakoda S; Hirose K
    Muscle Nerve; 2009 May; 39(5):666-73. PubMed ID: 19347921
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapy.
    Jackson CE; Barohn RJ; Ptacek LJ
    Muscle Nerve; 1994 Jul; 17(7):763-8. PubMed ID: 8008003
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Electromyography guides toward subgroups of mutations in muscle channelopathies.
    Fournier E; Arzel M; Sternberg D; Vicart S; Laforet P; Eymard B; Willer JC; Tabti N; Fontaine B
    Ann Neurol; 2004 Nov; 56(5):650-61. PubMed ID: 15389891
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.