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Items: 1 to 20 of 38

1.

Postoperative Hemiplegic Migraine After a Laparoscopic Cholecystectomy: A Case Report.

Happel J, Quiko AS, Phun H, Collier M, Mortensen A.

A A Case Rep. 2017 Apr 1;8(7):161-163. doi: 10.1213/XAA.0000000000000454.

PMID:
28045726
2.

Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.

Domitrz I, Kosiorek M, Żekanowski C, Kamińska A.

Hum Genomics. 2016 Jan 8;10:3. doi: 10.1186/s40246-015-0057-8.

3.

Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis: A Case Report.

LaBianca S, Jensen R, van den Maagdenberg AM, Baandrup L, Bendtsen L.

Headache. 2015 Jul-Aug;55(7):1004-7. doi: 10.1111/head.12595. Epub 2015 Jun 18.

PMID:
26087244
4.

Perfusion and pH MRI in familial hemiplegic migraine with prolonged aura.

Blicher JU, Tietze A, Donahue MJ, Smith SA, Østergaard L.

Cephalalgia. 2016 Mar;36(3):279-83. doi: 10.1177/0333102415586064. Epub 2015 May 6.

PMID:
25948653
5.

Field-testing of the ICHD-3 beta/proposed ICD-11 diagnostic criteria for migraine with aura.

Li D, Christensen AF, Olesen J.

Cephalalgia. 2015 Aug;35(9):748-56. doi: 10.1177/0333102414559731. Epub 2014 Nov 25.

PMID:
25424707
6.

Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.

Iizuka T, Tominaga N, Kaneko J, Sato M, Akutsu T, Hamada J, Sakai F, Nishiyama K.

J Neurol Neurosurg Psychiatry. 2015 Mar;86(3):344-53. doi: 10.1136/jnnp-2014-307731. Epub 2014 Jun 30.

PMID:
25411546
7.

Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice.

Vecchia D, Tottene A, van den Maagdenberg AM, Pietrobon D.

Neurobiol Dis. 2014 Sep;69:225-34. doi: 10.1016/j.nbd.2014.05.035. Epub 2014 Jun 5.

8.

The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal.

Barros J, Ruano L, Domingos J, Tuna A, Damásio J, Alonso I, Silveira I, Sequeiros J, Coutinho P.

Headache. 2014 May;54(5):911-5. doi: 10.1111/head.12260. Epub 2013 Oct 30.

PMID:
24898624
9.

Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i.

Di Guilmi MN, Wang T, Inchauspe CG, Forsythe ID, Ferrari MD, van den Maagdenberg AM, Borst JG, Uchitel OD.

J Neurosci. 2014 May 21;34(21):7047-58. doi: 10.1523/JNEUROSCI.2526-13.2014.

10.

Familial hemiplegic migraine: a model for the genetic studies of migraine.

Ducros A.

Cephalalgia. 2014 Nov;34(13):1035-7. doi: 10.1177/0333102414529192. Epub 2014 Apr 4. No abstract available.

PMID:
24707017
11.

Two novel SCN1A mutations identified in families with familial hemiplegic migraine.

Weller CM, Pelzer N, de Vries B, López MA, De Fàbregues O, Pascual J, Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM.

Cephalalgia. 2014 Nov;34(13):1062-9. doi: 10.1177/0333102414529195. Epub 2014 Apr 4.

PMID:
24707016
12.

Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.

Barros J, Ferreira A, Brandão AF, Lemos C, Correia F, Damásio J, Tuna A, Sequeiros J, Coutinho P, Alonso I, Pereira-Monteiro J.

Cephalalgia. 2014 Oct;34(12):1015-20. doi: 10.1177/0333102414527015. Epub 2014 Mar 19.

PMID:
24646837
13.

Pharmacological correction of gating defects in the voltage-gated Ca(v)2.1 Ca²⁺ channel due to a familial hemiplegic migraine mutation.

Inagaki A, Frank CA, Usachev YM, Benveniste M, Lee A.

Neuron. 2014 Jan 8;81(1):91-102. doi: 10.1016/j.neuron.2013.10.056.

14.

Relationship between intracellular Na+ concentration and reduced Na+ affinity in Na+,K+-ATPase mutants causing neurological disease.

Toustrup-Jensen MS, Einholm AP, Schack VR, Nielsen HN, Holm R, Sobrido MJ, Andersen JP, Clausen T, Vilsen B.

J Biol Chem. 2014 Feb 7;289(6):3186-97. doi: 10.1074/jbc.M113.543272. Epub 2013 Dec 19.

15.

Delayed recovery post anesthesia: an atypical presentation of familial hemiplegic migraine.

Greaney D, Vaughan P.

Can J Anaesth. 2014 Mar;61(3):278-9. doi: 10.1007/s12630-013-0090-9. Epub 2013 Dec 18. No abstract available.

PMID:
24347352
16.

Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.

Montani D, Girerd B, Günther S, Riant F, Tournier-Lasserve E, Magy L, Maazi N, Guignabert C, Savale L, Sitbon O, Simonneau G, Soubrier F, Humbert M.

Eur Respir J. 2014 Feb;43(2):641-3. doi: 10.1183/09031936.00147013. Epub 2013 Oct 17. No abstract available.

17.

The E1015K variant in the synprint region of the CaV2.1 channel alters channel function and is associated with different migraine phenotypes.

Condliffe SB, Fratangeli A, Munasinghe NR, Saba E, Passafaro M, Montrasio C, Ferrari M, Rosa P, Carrera P.

J Biol Chem. 2013 Nov 22;288(47):33873-83. doi: 10.1074/jbc.M113.497701. Epub 2013 Oct 9.

18.

Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects.

Cestèle S, Schiavon E, Rusconi R, Franceschetti S, Mantegazza M.

Proc Natl Acad Sci U S A. 2013 Oct 22;110(43):17546-51. doi: 10.1073/pnas.1309827110. Epub 2013 Oct 7.

19.

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.

Roth C, Freilinger T, Kirovski G, Dunkel J, Shah Y, Wilken B, Rautenstrauß B, Ferbert A.

Cephalalgia. 2014 Mar;34(3):183-90. doi: 10.1177/0333102413506128. Epub 2013 Oct 4.

PMID:
24096472
20.

Monozygotic twin sisters discordant for familial hemiplegic migraine.

Barros J, Barreto R, Brandão AF, Domingos J, Damásio J, Ramos C, Lemos C, Sequeiros J, Alonso I, Pereira-Monteiro J.

J Headache Pain. 2013 Sep 16;14:77. doi: 10.1186/1129-2377-14-77.

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