Similar articles for PMID: 19438926

Year	Number of Results
1985	1
1997	1
1999	3
2000	3
2001	9
2002	6
2003	5
2004	8
2005	9
2006	7
2007	9
2008	17
2009	13
2010	8
2011	7
2012	7
2013	9
2014	5
2015	3
2016	1
2017	6
2018	4
2019	3
2020	3
2021	7
2022	2
2023	5
2024	1

1

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.

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

[From gene to disease; from CACNA1A to migraine].

Kors EE, Haan J, Frants RR, Ferrari MD. Kors EE, et al. Ned Tijdschr Geneeskd. 2001 Feb 10;145(6):266-7. Ned Tijdschr Geneeskd. 2001. PMID: 11236374 Review. Dutch.

5

Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.

Kaja S, Van de Ven RC, Broos LA, Frants RR, Ferrari MD, Van den Maagdenberg AM, Plomp JJ. Kaja S, et al. J Neurophysiol. 2010 Sep;104(3):1445-55. doi: 10.1152/jn.00012.2010. Epub 2010 Jul 14. J Neurophysiol. 2010. PMID: 20631222 Free article.

6

Minor head trauma-induced sporadic hemiplegic migraine coma.

Curtain RP, Smith RL, Ovcaric M, Griffiths LR. Curtain RP, et al. Pediatr Neurol. 2006 Apr;34(4):329-32. doi: 10.1016/j.pediatrneurol.2005.08.033. Pediatr Neurol. 2006. PMID: 16638514

7

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

8

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.

9

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

10

FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.

Wiwanitkit V. Wiwanitkit V. J Neurol Sci. 2009 Feb 15;277(1-2):76-9. doi: 10.1016/j.jns.2008.10.012. Epub 2008 Nov 13. J Neurol Sci. 2009. PMID: 19007941

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

140 results

Results by year