Headache (including migraine)

Displaying results 1-8 of 8

• Mutation reports:

  Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing

  • R W Labrum,
  • S Rajakulendran,
  • T D Graves,
  • L H Eunson,
  • R Bevan,
  • M G Sweeney,
  • S R Hammans,
  • N Tubridy,
  • T Britton,
  • L J Carr,
  • J R Ostergaard,
  • C R Kennedy,
  • A Al-Memar,
  • D M Kullmann,
  • S Schorge,
  • K Temple,
  • M B Davis,
  • M G Hanna

  J. Med. Genet.  2009;46:786-791  doi:10.1136/jmg.2009.067967
  • [Abstract]
  • [Full text]
  • [PDF]
  • [web only appendix]
• Original articles:

  Clinical features in a family with an R460H mutation in transforming growth factor ß receptor 2 gene

  • C Law,
  • D Bunyan,
  • B Castle,
  • L Day,
  • I Simpson,
  • G Westwood,
  • B Keeton

  J. Med. Genet.  2006;43:908-916  doi:10.1136/jmg.2006.042176
  • [Abstract]
  • [Full text]
  • [PDF]
• Letters to JMG:

  A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

  • M T Bassi,
  • N Bresolin,
  • A Tonelli,
  • K Nazos,
  • F Crippa,
  • C Baschirotto,
  • C Zucca,
  • A Bersano,
  • D Dolcetta,
  • F M Boneschi,
  • V Barone,
  • G Casari

  J. Med. Genet.  2004;41:621-628  doi:10.1136/jmg.2003.017863
  • [Extract]
  • [Full text]
  • [PDF]
  • [Erratum]
• Online mutation reports:

  Clusters of non-truncating mutations of P/Q type Ca²⁺ channel subunit Ca_v2.1 causing episodic ataxia 2

  • E Mantuano,
  • L Veneziano,
  • M Spadaro,
  • P Giunti,
  • S Guida,
  • M G Leggio,
  • L Verriello,
  • N Wood,
  • C Jodice,
  • M Frontali

  J. Med. Genet.  2004;41:82  doi:10.1136/jmg.2003.015396
  • [Extract]
  • [Full text]
  • [PDF]
• Online mutation reports:

  Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip

  • V Shotelersuk,
  • C Ittiwut,
  • P Siriwan,
  • A Angspatt

  J. Med. Genet.  2003;40:64  doi:10.1136/jmg.40.5.e64
  • [Extract]
  • [Full text]
  • [PDF]
• Letters to JMG:

  Longevity in Schimke immuno-osseous dysplasia

  • S Lou,
  • P Lamfers,
  • N McGuire,
  • C F Boerkoel

  J. Med. Genet.  2002;39:922-925  doi:10.1136/jmg.39.12.922
  • [Extract]
  • [Full text]
  • [PDF]
• Review articles:

  Channelopathies: ion channel defects linked to heritable clinical disorders

  • Ricardo Felix

  J. Med. Genet.  2000;37:729-740  doi:10.1136/jmg.37.10.729
  • [Abstract]
  • [Full text]
  • [PDF]
• Original articles:

  The inheritance of migraine with aura estimated by means of structural equation modelling

  • Vibeke Ulrich,
  • Morten Gervil,
  • Kirsten O Kyvik,
  • Jes Olesen,
  • Michael B Russell

  J. Med. Genet.  1999;36:225-227  doi:10.1136/jmg.36.3.225
  • [Abstract]
  • [Full text]
  • [PDF]