378 related articles for article (PubMed ID: 11216900)
1. Inherited ion channel disorders.
Surtees R
Eur J Pediatr; 2000 Dec; 159 Suppl 3():S199-203. PubMed ID: 11216900
[TBL] [Abstract][Full Text] [Related]
2. Disorders of membrane channels or channelopathies.
Celesia GG
Clin Neurophysiol; 2001 Jan; 112(1):2-18. PubMed ID: 11137655
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Spectrum of Nondystrophic Skeletal Muscle Channelopathies in Children.
Al-Ghamdi F; Darras BT; Ghosh PS
Pediatr Neurol; 2017 May; 70():26-33. PubMed ID: 28325641
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Channelopathy].
Okamoto K; Ikeda Y
Rinsho Shinkeigaku; 2001 Dec; 41(12):1226-8. PubMed ID: 12235844
[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. 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]
9. Prevalence study of genetically defined skeletal muscle channelopathies in England.
Horga A; Raja Rayan DL; Matthews E; Sud R; Fialho D; Durran SC; Burge JA; Portaro S; Davis MB; Haworth A; Hanna MG
Neurology; 2013 Apr; 80(16):1472-5. PubMed ID: 23516313
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The neuronal channelopathies.
Kullmann DM
Brain; 2002 Jun; 125(Pt 6):1177-95. PubMed ID: 12023309
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Mutation spectrum and health status in skeletal muscle channelopathies in Japan.
Sasaki R; Nakaza M; Furuta M; Fujino H; Kubota T; Takahashi MP
Neuromuscul Disord; 2020 Jul; 30(7):546-553. PubMed ID: 32660787
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [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]
17. Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands.
Stunnenberg BC; Raaphorst J; Deenen JCW; Links TP; Wilde AA; Verbove DJ; Kamsteeg EJ; van den Wijngaard A; Faber CG; van der Wilt GJ; van Engelen BGM; Drost G; Ginjaar HB
Neuromuscul Disord; 2018 May; 28(5):402-407. PubMed ID: 29606556
[TBL] [Abstract][Full Text] [Related]
18. Muscle channelopathies.
Vivekanandam V; Jayaseelan D; Hanna MG
Handb Clin Neurol; 2023; 195():521-532. PubMed ID: 37562884
[TBL] [Abstract][Full Text] [Related]
19. Skeletal-muscle channelopathies: periodic paralysis and nondystrophic myotonias.
Ryan AM; Matthews E; Hanna MG
Curr Opin Neurol; 2007 Oct; 20(5):558-63. PubMed ID: 17885445
[TBL] [Abstract][Full Text] [Related]
20. Muscle channelopathies and electrophysiological approach.
Cherian A; Baheti NN; Kuruvilla A
Ann Indian Acad Neurol; 2008 Jan; 11(1):20-7. PubMed ID: 19966974
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]