Familial hemiplegic migraine, retinal degeneration...[Arch Neurol. 1970]

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1: Arch Neurol. 1970 Sep;23(3):201-9. Links

Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus.

PMID: 5311627 [PubMed - indexed for MEDLINE]

An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor.
Ann Neurol. 1980 Sep; 8(3):329-32.

[Ann Neurol. 1980]
Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
Ann Neurol. 1996 Jan; 39(1):100-6.

[Ann Neurol. 1996]
[Difficulties in the diagnosis of genetic deafness. 2 cases of Usher syndrome]
Rev Chir Oncol Radiol O R L Oftalmol Stomatol Otorinolaringol. 1982 Jan-Mar; 27(1):53-8.

[Rev Chir Oncol Radiol O R L Oftalmol Stomatol Otorinolaringol. 1982]
ReviewHereditary deafness in man.
N Engl J Med. 1969 Oct 2; 281(14):774-8 contd.

[N Engl J Med. 1969]
Review[Hemiplegic migraine]
Presse Med. 1995 Feb 25; 24(8):411-4.

[Presse Med. 1995]
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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, et al. Am J Hum Genet. 1999 Jan; 64(1):89-98.

[Am J Hum Genet. 1999]
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. Am J Hum Genet. 1994 Dec; 55(6):1166-72.

[Am J Hum Genet. 1994]

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