284 related articles for article (PubMed ID: 9623202)
1. [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]
2. Genetic neurological channelopathies.
Hanna MG
Nat Clin Pract Neurol; 2006 May; 2(5):252-63. PubMed ID: 16932562
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Calcium channelopathies in inherited neurological disorders: relevance to drug screening for acquired channel disorders.
Lory P; Mezghrani A
IDrugs; 2010 Jul; 13(7):467-71. PubMed ID: 20582871
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A review of the genetic relation between migraine and epilepsy.
Haan J; Terwindt GM; van den Maagdenberg AM; Stam AH; Ferrari MD
Cephalalgia; 2008 Feb; 28(2):105-13. PubMed ID: 18197881
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Channelopathy].
Okamoto K; Ikeda Y
Rinsho Shinkeigaku; 2001 Dec; 41(12):1226-8. PubMed ID: 12235844
[TBL] [Abstract][Full Text] [Related]
10. Molecular biology of channelopathies: impact on diagnosis and treatment.
Avanzini G; Franceschetti S; Avoni P; Liguori R
Expert Rev Neurother; 2004 May; 4(3):519-39. PubMed ID: 15853547
[TBL] [Abstract][Full Text] [Related]
11. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
Singh R; Macdonell RA; Scheffer IE; Crossland KM; Berkovic SF
Epileptic Disord; 1999 Jun; 1(2):93-9. PubMed ID: 10937138
[TBL] [Abstract][Full Text] [Related]
12. The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Vanmolkot KR; Babini E; de Vries B; Stam AH; Freilinger T; Terwindt GM; Norris L; Haan J; Frants RR; Ramadan NM; Ferrari MD; Pusch M; van den Maagdenberg AM; Dichgans M
Hum Mutat; 2007 May; 28(5):522. PubMed ID: 17397047
[TBL] [Abstract][Full Text] [Related]
13. Migraine and epilepsy: genetically linked?
Haan J; van den Maagdenberg AM; Brouwer OF; Ferrari MD
Expert Rev Neurother; 2008 Sep; 8(9):1307-11. PubMed ID: 18759542
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Mechanisms of human inherited epilepsies.
Reid CA; Berkovic SF; Petrou S
Prog Neurobiol; 2009 Jan; 87(1):41-57. PubMed ID: 18952142
[TBL] [Abstract][Full Text] [Related]
16. Epilepsy and ionic channels.
Roll P; Szepetowski P
Epileptic Disord; 2002 Sep; 4(3):165-72. PubMed ID: 12446218
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Neurological channelopathies.
Graves TD; Hanna MG
Postgrad Med J; 2005 Jan; 81(951):20-32. PubMed ID: 15640425
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Ion channels and neurological disorders].
Imoto K; Sasaki S
Nihon Shinkei Seishin Yakurigaku Zasshi; 2005 Aug; 25(4):189-96. PubMed ID: 16190368
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
