Similar articles for PMID: 18313928

Year	Number of Results
1953	1
1954	1
1955	1
1956	1
1958	2
1962	2
1969	1
1970	1
1979	1
1981	1
1999	3
2000	4
2001	9
2002	10
2003	4
2004	14
2005	15
2006	18
2007	22
2008	40
2009	32
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2013	16
2014	14
2015	5
2016	5
2017	6
2018	7
2019	2
2020	2
2021	4
2022	4
2023	3
2024	0

1

Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.

Chan YC, Burgunder JM, Wilder-Smith E, Chew SE, Lam-Mok-Sing KM, Sharma V, Ong BK. Chan YC, et al. J Clin Neurosci. 2008 Aug;15(8):891-4. doi: 10.1016/j.jocn.2007.01.013. Epub 2008 Mar 7. J Clin Neurosci. 2008. PMID: 18313928

2

Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.

Zangaladze A, Asadi-Pooya AA, Ashkenazi A, Sperling MR. Zangaladze A, et al. Epilepsy Behav. 2010 Feb;17(2):293-5. doi: 10.1016/j.yebeh.2009.12.017. Epub 2010 Jan 13. Epilepsy Behav. 2010. PMID: 20071244

3

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.

Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM. Stam AH, et al. Clin Genet. 2008 Nov;74(5):481-5. doi: 10.1111/j.1399-0004.2008.00996.x. Epub 2008 Apr 8. Clin Genet. 2008. PMID: 18400034

4

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

Thomsen LL, Kirchmann M, Bjornsson A, Stefansson H, Jensen RM, Fasquel AC, Petursson H, Stefansson M, Frigge ML, Kong A, Gulcher J, Stefansson K, Olesen J. Thomsen LL, et al. Brain. 2007 Feb;130(Pt 2):346-56. doi: 10.1093/brain/awl334. Epub 2006 Dec 2. Brain. 2007. PMID: 17142831

5

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.

Beauvais K, Cavé-Riant F, De Barace C, Tardieu M, Tournier-Lasserve E, Furby A. Beauvais K, et al. Eur Neurol. 2004;52(1):58-61. doi: 10.1159/000079546. Epub 2004 Jul 5. Eur Neurol. 2004. PMID: 15240985 No abstract available.

6

The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature.

Debiais S, Hommet C, Bonnaud I, Barthez MA, Rimbaux S, Riant F, Autret A. Debiais S, et al. Cephalalgia. 2009 Dec;29(12):1337-9. doi: 10.1111/j.1468-2982.2009.01884.x. Epub 2009 Apr 28. Cephalalgia. 2009. PMID: 19438926 Review.

7

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, Darcel F, Vicaut E, Bousser MG, Tournier-Lasserve E. Ducros A, et al. N Engl J Med. 2001 Jul 5;345(1):17-24. doi: 10.1056/NEJM200107053450103. N Engl J Med. 2001. PMID: 11439943 Free article.

8

CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2.

Robbins MS, Lipton RB, Laureta EC, Grosberg BM. Robbins MS, et al. Headache. 2009 Jul;49(7):1042-6. doi: 10.1111/j.1526-4610.2009.01464.x. Epub 2009 May 27. Headache. 2009. PMID: 19486177

9

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.

Stam AH, Luijckx GJ, Poll-Thé BT, Ginjaar IB, Frants RR, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM. Stam AH, et al. J Neurol Neurosurg Psychiatry. 2009 Oct;80(10):1125-9. doi: 10.1136/jnnp.2009.177279. Epub 2009 Jun 10. J Neurol Neurosurg Psychiatry. 2009. PMID: 19520699 Free article. Review.

10

[Familial hemiplegic migraine resulting in recurrent coma].

Lee H, Aramideh M, Ginjaar HB. Lee H, et al. Ned Tijdschr Geneeskd. 2008 Feb 16;152(7):393-6. Ned Tijdschr Geneeskd. 2008. PMID: 18380388 Dutch.

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