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 *

241 related articles for article (PubMed ID: 20824453)

  • 1. Hereditary channelopathies in neurology.
    Jurkat-Rott K; Lerche H; Weber Y; Lehmann-Horn F
    Adv Exp Med Biol; 2010; 686():305-34. PubMed ID: 20824453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Muscle channelopathies and related diseases.
    Fontaine B
    Handb Clin Neurol; 2013; 113():1433-6. PubMed ID: 23622365
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inherited ion channel disorders.
    Surtees R
    Eur J Pediatr; 2000 Dec; 159 Suppl 3():S199-203. PubMed ID: 11216900
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Ion channel abnormalities ("channelopathies") in neurologic diseases].
    Masson C
    Presse Med; 2002 Feb; 31(6):244-8. PubMed ID: 11883365
    [TBL] [Abstract][Full Text] [Related]  

  • 5. State of the art in hereditary muscle channelopathies.
    Jurkat-Rott K; Lehmann-Horn F
    Acta Myol; 2010 Oct; 29(2):343-50. PubMed ID: 21314017
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders].
    Terwindt GM; Ophoff RA; Haan J; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 1998 May; 142(18):1015-9. PubMed ID: 9623202
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neurological disorders caused by inherited ion-channel mutations.
    Kullmann DM; Hanna MG
    Lancet Neurol; 2002 Jul; 1(3):157-66. PubMed ID: 12849484
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system.
    Ptácek LJ
    Neuromuscul Disord; 1997 Jun; 7(4):250-5. PubMed ID: 9196907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics, an alternative way to discover, characterize and understand ion channels.
    Schofield PR
    Clin Exp Pharmacol Physiol; 2001; 28(1-2):84-8. PubMed ID: 11153544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ion channel shake-down.
    Ptácek L
    Nat Genet; 1994 Oct; 8(2):111-2. PubMed ID: 7531055
    [No Abstract]   [Full Text] [Related]  

  • 11. Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias.
    Platt D; Griggs R
    Curr Opin Neurol; 2009 Oct; 22(5):524-31. PubMed ID: 19571750
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic neurological channelopathies.
    Hanna MG
    Nat Clin Pract Neurol; 2006 May; 2(5):252-63. PubMed ID: 16932562
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscle channelopathies.
    Statland J; Phillips L; Trivedi JR
    Neurol Clin; 2014 Aug; 32(3):801-15, x. PubMed ID: 25037091
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Channelopathies: the nondystrophic myotonias and periodic paralyses.
    Lehmann-Horn F; Rüdel R
    Semin Pediatr Neurol; 1996 Jun; 3(2):122-39. PubMed ID: 8795846
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Channelopathies in neurology].
    Grippo J; Grippo T
    Rev Neurol; 2001 Oct 1-15; 33(7):643-7. PubMed ID: 11784953
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Channelopathy].
    Okamoto K; Ikeda Y
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1226-8. PubMed ID: 12235844
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Periodic paralysis, myotonia congenita and sarcolemmal ion channels: a success of the candidate gene approach.
    Fontaine B
    Neuromuscul Disord; 1993 Mar; 3(2):101-7. PubMed ID: 7689379
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscle channelopathies: the nondystrophic myotonias and periodic paralyses.
    Statland JM; Barohn RJ
    Continuum (Minneap Minn); 2013 Dec; 19(6 Muscle Disease):1598-614. PubMed ID: 24305449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Is there a role for potassium channel openers in neuronal ion channel disorders?
    Lawson K
    Expert Opin Investig Drugs; 2000 Oct; 9(10):2269-80. PubMed ID: 11060806
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.
    Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD
    Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.