Literature DB >> 5311627

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

G F Young, C A Leon-Barth, J Green.   

Abstract

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Mesh：

Year:  1970        PMID： 5311627     DOI： 10.1001/archneur.1970.00480270011002

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  3 in total

Review 1.  The cerebellum and migraine.

Authors:  Maurice Vincent; Nouchine Hadjikhani
Journal:  Headache       Date:  2007-06       Impact factor: 5.887

2.  Genetic heterogeneity of familial hemiplegic migraine.

Authors:  A Joutel; A Ducros; K Vahedi; P Labauge; O Delrieu; N Pinsard; J Mancini; G Ponsot; F Gouttière; J L Gastaut
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

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

Authors:  A Ducros; C Denier; A Joutel; K Vahedi; A Michel; F Darcel; M Madigand; D Guerouaou; F Tison; J Julien; E Hirsch; F Chedru; C Bisgård; G Lucotte; P Després; C Billard; M A Barthez; G Ponsot; M G Bousser; E Tournier-Lasserve
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025
  3 in total

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