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Items: 1 to 20 of 666

1.

[Case of sporadic hemiplegic migraine with cerebellar ataxia].

Iwanaka Y, Okada K, Akamatsu N, Uozumi T, Adachi Y, Tsuji S.

Rinsho Shinkeigaku. 2009 May;49(5):267-70. Japanese.

PMID:
19594104
2.

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.

Terwindt G, Kors E, Haan J, Vermeulen F, Van den Maagdenberg A, Frants R, Ferrari M.

Arch Neurol. 2002 Jun;59(6):1016-8. Review.

PMID:
12056940
3.

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD.

Neurology. 1998 Apr;50(4):1105-10.

PMID:
9566402
4.

[A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset].

Ohkuma Y, Sato K, Ohtomo T, Ohishi H, Mitsuoka H, Mori H, Hirai S, Takubo H, Takeda N, Sato K, Mizuno Y.

No To Shinkei. 1997 May;49(5):473-81. Japanese.

PMID:
9163763
5.

1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1.

Dichgans M, Herzog J, Freilinger T, Wilke M, Auer DP.

Neurology. 2005 Feb 22;64(4):608-13.

PMID:
15728280
6.

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.

Wada T, Kobayashi N, Takahashi Y, Aoki T, Watanabe T, Saitoh S.

Pediatr Neurol. 2002 Jan;26(1):47-50.

PMID:
11814735
7.

[A case of cerebellar ataxia showing severe dystonia masquerading as myoclonic jerky movements on arm extension].

Nakagaki H, Furuya H, Miyoshi Y, Murai H, Araki T, Ohyagi Y, Yamada T, Sasaki M, Tobimatsu S, Kira J.

Rinsho Shinkeigaku. 2002 Jan;42(1):7-12. Japanese.

PMID:
12355858
8.

[Hemiplegic migraine complicated with coronary vasospasm].

Takeuchi I, Hata T, Itagaki H, Akutsu T, Takagi Y.

Rinsho Shinkeigaku. 1992 Jan;32(1):73-7. Japanese.

PMID:
1628439
9.

Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.

Elliott MA, Peroutka SJ, Welch S, May EF.

Ann Neurol. 1996 Jan;39(1):100-6.

PMID:
8572654
10.

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.

Brain. 2007 Feb;130(Pt 2):346-56. Epub 2006 Dec 2.

PMID:
17142831
11.

Sporadic hemiplegic migraine presenting as acute encephalopathy.

Ohmura K, Suzuki Y, Saito Y, Wada T, Goto M, Seto S.

Brain Dev. 2012 Sep;34(8):691-5. doi: 10.1016/j.braindev.2011.11.002. Epub 2011 Dec 1.

PMID:
22136990
12.

Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.

Zangaladze A, Asadi-Pooya AA, Ashkenazi A, Sperling MR.

Epilepsy Behav. 2010 Feb;17(2):293-5. doi: 10.1016/j.yebeh.2009.12.017. Epub 2010 Jan 13.

PMID:
20071244
13.

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.

Vahedi K, Denier C, Ducros A, Bousson V, Levy C, Chabriat H, Haguenau M, Tournier-Lasserve E, Bousser MG.

Neurology. 2000 Oct 10;55(7):1040-2.

PMID:
11061267
14.

[Familial hemiplegic migraine resulting in recurrent coma].

Lee H, Aramideh M, Ginjaar HB.

Ned Tijdschr Geneeskd. 2008 Feb 16;152(7):393-6. Dutch.

PMID:
18380388
15.

[A 32-year-old man who developed a posterior fossa mass 12 years after the radiation therapy for cerebellar arteriovenous malformation].

Koshimura I, Takeda N, Ohtomo T, Shimada J, Sugano K, Mori H, Mizuno Y, Sato K.

No To Shinkei. 1996 Jan;48(1):81-9. Japanese.

PMID:
8679325
16.

Genetic heterogeneity in Italian families with familial hemiplegic migraine.

Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C.

Neurology. 1999 Jul 13;53(1):26-33.

PMID:
10408532
17.

[A sporadic case of episodic ataxia with nystagmus (EA-2)].

Namekawa M, Takiyama Y, Ueno N, Nishizawa M.

Rinsho Shinkeigaku. 1998 May;38(5):446-9. Japanese.

PMID:
9805992
18.

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.

N Engl J Med. 2001 Jul 5;345(1):17-24.

19.

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E.

Am J Hum Genet. 1999 Jan;64(1):89-98.

20.

A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline.

Freilinger T, Ackl N, Ebert A, Schmidt C, Rautenstrauss B, Dichgans M, Danek A.

J Neurol Sci. 2011 Jan 15;300(1-2):160-3. doi: 10.1016/j.jns.2010.09.032. Epub 2010 Oct 28.

PMID:
21035146

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