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Items: 1 to 20 of 158

1.

Familial migraine with vertigo and essential tremor.

Baloh RW, Foster CA, Yue Q, Nelson SF.

Neurology. 1996 Feb;46(2):458-60.

PMID:
8614512
2.

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR.

Genomics. 1994 Jul 1;22(1):21-6.

PMID:
7959770
3.

Familial migraine with vertigo: no mutations found in CACNA1A.

Kim JS, Yue Q, Jen JC, Nelson SF, Baloh RW.

Am J Med Genet. 1998 Sep 1;79(2):148-51.

PMID:
9741473
4.

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD.

Epilepsia. 1997 Aug;38(8):915-21.

5.

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
6.

Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.

Hovatta I, Kallela M, Färkkilä M, Peltonen L.

Genomics. 1994 Oct;23(3):707-9.

PMID:
7851903
7.

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF.

Hum Mol Genet. 2006 Jan 15;15(2):251-8. Epub 2005 Dec 5.

8.

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.

Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, Verier A, Echenne B, Lopez de Munain A, Bousser MG, Tournier-Lasserve E.

Ann Neurol. 1997 Dec;42(6):885-90.

PMID:
9403481
9.

Genetic heterogeneity of familial hemiplegic migraine.

Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al.

Am J Hum Genet. 1994 Dec;55(6):1166-72.

10.

Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.

Baloh RW, Yue Q, Furman JM, Nelson SF.

Ann Neurol. 1997 Jan;41(1):8-16.

PMID:
9005860
11.

Familial benign recurrent vertigo.

Oh AK, Lee H, Jen JC, Corona S, Jacobson KM, Baloh RW.

Am J Med Genet. 2001 May 15;100(4):287-91.

PMID:
11343320
12.

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

Steckley JL, Ebers GC, Cader MZ, McLachlan RS.

Neurology. 2001 Oct 23;57(8):1499-502.

PMID:
11673600
13.

An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor.

Zifkin B, Andermann E, Andermann F, Kirkham T.

Ann Neurol. 1980 Sep;8(3):329-32.

PMID:
7436378
14.

A gene for familial hemiplegic migraine maps to chromosome 19.

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al.

Nat Genet. 1993 Sep;5(1):40-5.

PMID:
8220421
15.

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families.

Ahmed MA, Reid E, Cooke A, Arngrímsson R, Tolmie JL, Stephenson JB.

J Neurol Neurosurg Psychiatry. 1996 Dec;61(6):616-20.

16.

[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al.

Rev Neurol (Paris). 1994;150(5):340-5. French.

PMID:
7878319
17.

Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.

Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR.

Neurology. 1998 May;50(5):1428-32.

PMID:
9596000
18.

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.

19.

Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy.

Jen JC, Wang H, Lee H, Sabatti C, Trent R, Hannigan I, Brantberg K, Halmagyi GM, Nelson SF, Baloh RW.

Neurology. 2004 Dec 28;63(12):2376-9.

PMID:
15623703
20.

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.

Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ.

Genomics. 2001 Dec;78(3):150-4.

PMID:
11735221
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