BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

354 related articles for article (PubMed ID: 11137655)

  • 1. Disorders of membrane channels or channelopathies.
    Celesia GG
    Clin Neurophysiol; 2001 Jan; 112(1):2-18. PubMed ID: 11137655
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. [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]  

  • 4. Voltage-gated ion channels and hereditary disease.
    Lehmann-Horn F; Jurkat-Rott K
    Physiol Rev; 1999 Oct; 79(4):1317-72. PubMed ID: 10508236
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ion channels and epilepsy.
    Lerche H; Jurkat-Rott K; Lehmann-Horn F
    Am J Med Genet; 2001; 106(2):146-59. PubMed ID: 11579435
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies.
    Meola G; Sansone V; Rotondo G; Mancinelli E
    Eur J Histochem; 2003; 47(1):17-28. PubMed ID: 12685554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Ion channel diseases in neurology].
    Lerche H; Mitrovic N; Lehmann-Horn F
    Fortschr Neurol Psychiatr; 1997 Nov; 65(11):481-8. PubMed ID: 9480290
    [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. [Channelopathy].
    Okamoto K; Ikeda Y
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1226-8. PubMed ID: 12235844
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ion channels-related diseases.
    Dworakowska B; Dołowy K
    Acta Biochim Pol; 2000; 47(3):685-703. PubMed ID: 11310970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular genetics of human familial epilepsy syndromes.
    Hirose S; Okada M; Kaneko S; Mitsudome A
    Epilepsia; 2002; 43 Suppl 9():21-5. PubMed ID: 12383275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Calcium channels and channelopathies of the central nervous system.
    Pietrobon D
    Mol Neurobiol; 2002 Feb; 25(1):31-50. PubMed ID: 11890456
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The neuronal channelopathies.
    Kullmann DM
    Brain; 2002 Jun; 125(Pt 6):1177-95. PubMed ID: 12023309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic abnormalities underlying familial epilepsy syndromes.
    Hirose S; Okada M; Yamakawa K; Sugawara T; Fukuma G; Ito M; Kaneko S; Mitsudome A
    Brain Dev; 2002 Jun; 24(4):211-22. PubMed ID: 12015163
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Periodic paralysis: understanding channelopathies.
    Lehmann-Horn F; Jurkat-Rott K; Rüdel R
    Curr Neurol Neurosci Rep; 2002 Jan; 2(1):61-9. PubMed ID: 11898585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic approach to the pathogeneses of epilepsy].
    Hirose S
    Rinsho Shinkeigaku; 2004 Nov; 44(11):975-8. PubMed ID: 15651347
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits.
    McKeown L; Robinson P; Jones OT
    Acta Pharmacol Sin; 2006 Jul; 27(7):799-812. PubMed ID: 16787562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ion channels and epilepsy.
    Armijo JA; Shushtarian M; Valdizan EM; Cuadrado A; de las Cuevas I; Adín J
    Curr Pharm Des; 2005; 11(15):1975-2003. PubMed ID: 15974971
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetics of infantile nervous system channelopathies.
    Gardiner M
    Early Hum Dev; 2006 Dec; 82(12):775-9. PubMed ID: 17049761
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Channelopathies: ion channel defects linked to heritable clinical disorders.
    Felix R
    J Med Genet; 2000 Oct; 37(10):729-40. PubMed ID: 11015449
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.