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Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations

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References

  1. (2004) The International Classification of Headache Disorders, 2nd edn. Cephalalgia 24(suppl 1): 9160

  2. Black DF (2006) Sporadic and familial hemiplegic migraine: diagnosis and treatment. Semin Neurol 26:208–216

    Article  PubMed  Google Scholar 

  3. De Benedittis G, Ferrari Da Passano C, Granata G, Lorenzetti A (1999) CBF changes during headache-free periods and spontaneous/induced attacks in migraine with and without aura: a TCD and SPECT comparison study. J Neurosurg Sci 43:141–146 (discussion 146-147)

  4. De Fusco M, Marconi R, Silvestri L, Atorino L, Rampoldi L, Morgante L, Ballabio A, Aridon P, Casari G (2003) Haploinsufficiency of ATP1A2 encoding the Na +/K + pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 33:192–196

    Article  PubMed  Google Scholar 

  5. Ducros A, Boukobza M, Porcher R, Sarov M, Valade D, Bousser MG (2007) The clinical and radiological spectrum of reversible cerebral vasoconstriction syndrome. A prospective series of 67 patients. Brain 130:3091–3101

    Article  PubMed  Google Scholar 

  6. Gomez-Aranda F, Canadillas F, Marti-Masso JF, Diez-Tejedor E, Serrano PJ, Leira R, Gracia M, Pascual J (1997) Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis. A report of 50 cases. Brain 120(Pt 7):1105–1113

    Article  PubMed  Google Scholar 

  7. Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87:543–552

    Article  PubMed  CAS  Google Scholar 

  8. Pierelli F, Pauri F, Cupini LM, Fiermonte G, Rizzo PA (1991) Transcranial doppler sonography in familial hemiplegic migraine. Cephalalgia 11:29–31

    Article  PubMed  CAS  Google Scholar 

  9. Prodan CI, Holland NR, Lenaerts ME, Parke JT (2002) Magnetic resonance angiogram evidence of vasospasm in familial hemiplegic migraine. J Child Neurol 17:470–472

    Article  PubMed  Google Scholar 

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Conflicts of interest

All authors declare no conflict of interest for this study.

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The study was performed according to the Medical Association's professional code of conduct of Saxonia/Germany.

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Correspondence to Andreas Hermann.

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Hermann, A., Engelandt, K., Rautenstrauss, B. et al. Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations. J Neurol 260, 2172–2174 (2013). https://doi.org/10.1007/s00415-013-7010-3

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  • DOI: https://doi.org/10.1007/s00415-013-7010-3

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