Literature DB >> 15115644

Toward a molecular genetic classification of familial hemiplegic migraine.

Joost Haan1, Esther E Kors, Arn M J M van den Maagdenberg, Kaate R J Vanmolkot, Gisela M Terwindt, Rune R Frants, Michel D Ferrari.   

Abstract

The genetics of migraine is a fascinating and rapidly moving research area. Familial hemiplegic migraine, a rare subtype of migraine with a Mendelian pattern of inheritance, is caused by mutations in the chromosome 19 CACNA1A gene or in the chromosome 1 ATP1A2 gene. Familial migraine variants are classified on the basis of clinical, descriptive criteria, but this is insufficient. In the future, a diagnostic classification based on mutation-analysis is needed.

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Year:  2004        PMID： 15115644     DOI： 10.1007/s11916-004-0058-0

Source DB:  PubMed          Journal:  Curr Pain Headache Rep        ISSN： 1534-3081


  35 in total

1.  Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.

Authors:  T Takahashi; S Igarashi; T Kimura; I Hozumi; I Kawachi; O Onodera; H Takano; M Saito; S Tsuji
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-05       Impact factor: 10.154

2.  The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

Authors:  A Ducros; C Denier; A Joutel; M Cecillon; C Lescoat; K Vahedi; F Darcel; E Vicaut; M G Bousser; E Tournier-Lasserve
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

Review 3.  Genetic epidemiology of migraine and cluster headache.

Authors:  M B Russell
Journal:  Cephalalgia       Date:  1997-10       Impact factor: 6.292

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

Authors:  G M Terwindt; R A Ophoff; J Haan; M N Vergouwe; R van Eijk; R R Frants; M D Ferrari
Journal:  Neurology       Date:  1998-04       Impact factor: 9.910

5.  A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.

Authors:  L L Thomsen; M K Eriksen; S F Roemer; I Andersen; J Olesen; M B Russell
Journal:  Brain       Date:  2002-06       Impact factor: 13.501

Review 6.  The genetics of migraine: implication for treatment approaches.

Authors:  M D Ferrari; J Haan
Journal:  J Neural Transm Suppl       Date:  2002

7.  A gene for familial hemiplegic migraine maps to chromosome 19.

Authors:  A Joutel; M G Bousser; V Biousse; P Labauge; H Chabriat; A Nibbio; J Maciazek; B Meyer; M A Bach; J Weissenbach
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

8.  Genetic heterogeneity of familial hemiplegic migraine.

Authors:  R A Ophoff; R van Eijk; L A Sandkuijl; G M Terwindt; C P Grubben; J Haan; D Lindhout; M D Ferrari; R R Frants
Journal:  Genomics       Date:  1994-07-01       Impact factor: 5.736

9.  Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.

Authors:  Roberto Marconi; Maurizio De Fusco; Paolo Aridon; Katrin Plewnia; Maja Rossi; Sadia Carapelli; Andrea Ballabio; Letterio Morgante; Rosa Musolino; Antonio Epifanio; Giuseppe Micieli; Giuseppe De Michele; Giorgio Casari
Journal:  Ann Neurol       Date:  2003-03       Impact factor: 10.422

10.  Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

Authors:  Maurizio De Fusco; Roberto Marconi; Laura Silvestri; Luigia Atorino; Luca Rampoldi; Letterio Morgante; Andrea Ballabio; Paolo Aridon; Giorgio Casari
Journal:  Nat Genet       Date:  2003-01-21       Impact factor: 38.330
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  1 in total

1.  Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures.

Authors:  Rokhsareh Meamar; Maryam Ostadsharif; Mohammad Saadatnia; Abbas Ghorbani; Nayereh Nouri; Leila Dehghani; Mansoor Salehi
Journal:  J Res Med Sci       Date:  2013-03       Impact factor: 1.852
  1 in total

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