290 related articles for article (PubMed ID: 12420087)
1. Skeletal muscle channelopathies.
Jurkat-Rott K; Lerche H; Lehmann-Horn F
J Neurol; 2002 Nov; 249(11):1493-502. PubMed ID: 12420087
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetics of ion channel diseases.
George AL
Kidney Int; 1995 Oct; 48(4):1180-90. PubMed ID: 8569079
[TBL] [Abstract][Full Text] [Related]
3. Human muscle voltage-gated ion channels and hereditary disease.
Jurkat-Rott K; Lehmann-Horn F
Curr Opin Pharmacol; 2001 Jun; 1(3):280-7. PubMed ID: 11712752
[TBL] [Abstract][Full Text] [Related]
4. Ion channels-related diseases.
Dworakowska B; Dołowy K
Acta Biochim Pol; 2000; 47(3):685-703. PubMed ID: 11310970
[TBL] [Abstract][Full Text] [Related]
5. Ion channels and disorders of excitation in skeletal muscle.
Barchi RL
Curr Opin Neurol Neurosurg; 1993 Feb; 6(1):40-7. PubMed ID: 7679017
[TBL] [Abstract][Full Text] [Related]
6. [The spectrum of hereditary skeletal-muscle channelopathies].
Trip J; Drost G; Ginjaar HB; van Engelen BG; Faber CG
Ned Tijdschr Geneeskd; 2005 Sep; 149(38):2093-8. PubMed ID: 16201598
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Inherited ion channel disorders.
Surtees R
Eur J Pediatr; 2000 Dec; 159 Suppl 3():S199-203. PubMed ID: 11216900
[TBL] [Abstract][Full Text] [Related]
9. Ryanodine receptor channelopathies.
Benkusky NA; Farrell EF; Valdivia HH
Biochem Biophys Res Commun; 2004 Oct; 322(4):1280-5. PubMed ID: 15336975
[TBL] [Abstract][Full Text] [Related]
10. The role of ion-regulatory membrane proteins of excitation-contraction coupling and relaxation in inherited muscle diseases.
Froemming GR; Ohlendieck K
Front Biosci; 2001 Jan; 6():D65-74. PubMed ID: 11145921
[TBL] [Abstract][Full Text] [Related]
11. Therapy in myotonic disorders and in muscle channelopathies.
Meola G; Sansone V
Neurol Sci; 2000; 21(5 Suppl):S953-61. PubMed ID: 11382195
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Ion-channel related muscular diseases].
Fontaine B
Rev Med Interne; 1999 Sep; 20(9):774-80. PubMed ID: 10522299
[TBL] [Abstract][Full Text] [Related]
14. [Channelopathy].
Okamoto K; Ikeda Y
Rinsho Shinkeigaku; 2001 Dec; 41(12):1226-8. PubMed ID: 12235844
[TBL] [Abstract][Full Text] [Related]
15. Electrophysiology and molecular pharmacology of muscle channelopathies.
Jurkat-Rott K; Lehmann-Horn F
Rev Neurol (Paris); 2004 May; 160(5 Pt 2):S43-8. PubMed ID: 15269660
[TBL] [Abstract][Full Text] [Related]
16. [Myocyte sarcolemmal and cytoskeleton proteins in inherited muscular diseases].
Carpén O
Duodecim; 2003; 119(3):179-86. PubMed ID: 12650015
[No Abstract] [Full Text] [Related]
17. [Myotonia and channelopathy].
Kurihara T
Rinsho Shinkeigaku; 1999 Dec; 39(12):1219-21. PubMed ID: 10791081
[TBL] [Abstract][Full Text] [Related]
18. Ion channel mutations and diseases of skeletal muscle.
Barchi RL
Neurobiol Dis; 1997; 4(3-4):254-64. PubMed ID: 9361302
[TBL] [Abstract][Full Text] [Related]
19. Dynamic alterations in myoplasmic Ca2+ in malignant hyperthermia and central core disease.
Lyfenko AD; Goonasekera SA; Dirksen RT
Biochem Biophys Res Commun; 2004 Oct; 322(4):1256-66. PubMed ID: 15336973
[TBL] [Abstract][Full Text] [Related]
20. A Mixed Periodic Paralysis & Myotonia Mutant, P1158S, Imparts pH-Sensitivity in Skeletal Muscle Voltage-gated Sodium Channels.
Ghovanloo MR; Abdelsayed M; Peters CH; Ruben PC
Sci Rep; 2018 Apr; 8(1):6304. PubMed ID: 29674667
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]