Literature DB >> 11971066

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

T Takahashi, S Igarashi, T Kimura, I Hozumi, I Kawachi, O Onodera, H Takano, M Saito, S Tsuji.   

Abstract

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Year:  2002        PMID： 11971066      PMCID： PMC1737889          DOI： 10.1136/jnnp.72.5.676-a

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  5 in total

Review 1.  Migraine genetics: an update.

Authors:  J Haan; E E Kors; Kaate R J Vanmolkot; Arn M J M van den Maagdenberg; Rune R Frants; M D Ferrari
Journal:  Curr Pain Headache Rep       Date:  2005-06

2.  Crosslinguistic application of English-centric rhythm descriptors in motor speech disorders.

Authors:  Julie M Liss; Rene Utianski; Kaitlin Lansford
Journal:  Folia Phoniatr Logop       Date:  2013-05-28       Impact factor: 0.849

Review 3.  Toward a molecular genetic classification of familial hemiplegic migraine.

Authors:  Joost Haan; Esther E Kors; Arn M J M van den Maagdenberg; Kaate R J Vanmolkot; Gisela M Terwindt; Rune R Frants; Michel D Ferrari
Journal:  Curr Pain Headache Rep       Date:  2004-06

4.  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

5.  An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation.

Authors:  Satoshi Kono; Tatsuhiro Terada; Yasuomi Ouchi; Hiroaki Miyajima
Journal:  BBA Clin       Date:  2014-09-28
  5 in total

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