Eurohead Project: Migraine genes and neurobiological pathways

Association between cortical metabolite levels and clinical manifestations of migrainous aura: an MR-spectroscopy study.

Schulz UG, Blamire AM, Corkill RG, Davies P, Styles P, Rothwell PM.

Brain. 2007 Oct 22; [Epub ahead of print]

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KR, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM, van den Maagdenberg AM.

J Hum Genet. 2007 Oct 19; [Epub ahead of print]

Investigation of neuromuscular transmission in some rare types of migraine.

Baslo MB, Coban A, Baykan B, Tutkavul K, Karli N, Saip S, Orhan EK, Ertas M.

Cephalalgia 2007;27:1201-5.

Familial hemiplegic migraine: permanent attack-related neurologic deficits.

Dodick D, Roarke M.

Headache 2007;47:1210-2.

Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.

Tonelli A, Gallanti A, Bersano A, Cardin V, Ballabio E, Airoldi G, Redaelli F, Candelise L, Bresolin N, Bassi M.

Clin Genet. 2007 Sep 18; [Epub ahead of print]

Treatment of hemiplegic migraine with triptans.

Artto V, Nissilä M, Wessman M, Palotie A, Färkkilä M, Kallela M.

Eur J Neurol 2007;14:1053-6.

Association analysis of chromosome 1 migraine candidate genes.

Fernandez F, Curtain RP, Colson NJ, Ovcaric M, MacMillan J, Griffiths LRBMC.

Med Genet 2007;8:57.

Apnoeic spells following general anaesthesia in a patient with familial hemiplegic migraine.

Willson J, Kapur S.

Anaesthesia 2007;62:956-8.

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.

Ragno M, Cacchiò G, Fabrizi GM, Scarcella M, Silvaggio F, Cavallaro T, Taioli F, Trojano L.

Neurol Sci 2007;28:181-4.

Adult-onset hemiplegic migraine with cortical enhancement and oedema.

Cha YH, Millett D, Kane M, Jen J, Baloh R.

Cephalalgia 2007 Jul 23; [Epub ahead of print]

Hemiplegic migraine: Hyperperfusion and abortive therapy with intravenous verapamil.

Hsu DA, Stafstrom CE, Rowley HA, Kiff JE, Dulli DA.

Brain Dev 2007 Jul 3; [Epub ahead of print]

Migraine with aura is a risk factor for cardiovascular and cerebrovascular disease: a critically appraised topic.

Wingerchuk DM, Spencer B, Dodick DW, Demaerschalk BM.

Neurologist 2007;13:231-3.

Presentation of hemiplegic migraine--hemiplegia and hemi-sensory loss following general anaesthesia.

Lin L, Adey C.

Anaesth Intensive Care 2007;35:418-22.

Cessation of hemiplegic migraine auras with greater occipital nerve blockade.

Rozen T.

Headache 2007;47:917-9.

Migraine: gene mutations and functional consequences.

van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD.

Curr Opin Neurol 2007;20:299-305.

First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.

Vanmolkot KR, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJ, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM.

Eur J Hum Genet 2007; May 2 [Epub ahead of print]

Prolonged hemiplegic episodes in children due to mutations in ATP1A2.

Jen JC, Klein A, Boltshauser E, Cartwright MS, Roach ES, Mamsa H, Baloh RW.

J Neurol Neurosurg Psychiatry 2007;78:523-6.

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

Vanmolkot KR, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AM, Dichgans M.

Hum Mutat 2007;28:522.

Familial hemiplegic migraine.

Pietrobon D.

Neurotherapeutics 2007;4:274-84.

Familial occipitotemporal lobe epilepsy and migraine with visual aura. Linkage to chromosome 9q.

Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P.

Neurology 2007; Apr 25 [Epub ahead of print]

Functional polymorphisms of the 5-HT1A and 5-HT1B receptor are associated with clinical symptoms in migraineurs.

Marziniak M, Mossner R, Kienzler C, Riederer P, Lesch KP, Sommer C.

J Neural Transm 2007; Apr 10 [Epub ahead of print]

Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.

Xie G, Clapcote SJ, Nieman BJ, Tallerico T, Huang Y, Vukobradovic I, Cordes SP, Osborne LR, Rossant J, Sled JG, Henderson JT, Roder JC.

Genes Brain Behav 2007; Mar 21; [Epub ahead of print]

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.

Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C.

J Neurol Sci 2007;254:69-71.

Combined effects of ACE and MMP-3 polymorphisms on migraine development.

Kara I, Ozkok E, Aydin M, Orhan N, Cetinkaya Y, Gencer M, Kilic G, Tireli H.

Cephalalgia 2007;27:235-43.

Establishing the genetic heterogeneity of familial hemiplegic migraine.

Low N, Singleton A.

Brain 2007;130:312-3.

The search for migraine genes: an overview of current knowledge.

Colson NJ, Fernandez F, Lea RA, Griffiths LR.

Cell Mol Life Sci 2007;64:331-44.

The influence of gender and sex steroids on craniofacial nociception.

Cairns BE.

Headache 2007;47:319-24.

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

Thomsen LL, Kirchmann M, Bjornsson A, Stefansson H, Jensen RM, Fasquel AC, Petursson H, Stefansson M, Frigge ML, Kong A, Gulcher J, Stefansson K, Olesen J.

Brain 2007;130:346-56.

Recent advances in understanding migraine mechanisms, molecules and therapeutics.

Goadsby PJ.

Trends Mol Med 2007;13:39-44.

Deficiency in Na,K-ATPase alpha isoform genes alters spatial learning, motor activity, and anxiety in mice.

Moseley AE, Williams MT, Schaefer TL, Bohanan CS, Neumann JC, Behbehani MM, Vorhees CV, Lingrel JB.

J Neurosci 2007;27:616-26.