Jose M. Monteiro-Pereira
Porto, Portugal
Last Updated: 09/26/2026
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Found 12 publications
A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study.
A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study.
Journal: The journal of headache and pain
Published: December 10, 2020
Chronic and Refractory Migraine: How to Diagnose and Treat
Journal: Acta medica portuguesa
Published: March 01, 2019
CADASIL: MRI may be normal in the fourth decade of life - a case report.
Journal: Cephalalgia : an international journal of headache
Published: December 10, 2015
Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.
Journal: Cephalalgia : an international journal of headache
Published: March 21, 2014
Monozygotic twin sisters discordant for familial hemiplegic migraine.
Journal: The journal of headache and pain
Published: July 17, 2013
Interaction between γ-aminobutyric acid A receptor genes: new evidence in migraine susceptibility.
Journal: PloS one
Published: May 13, 2013
Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.
Journal: JAMA neurology
Published: February 15, 2013
Assessing risk factors for migraine: differences in gender transmission.
Journal: PloS one
Published: August 30, 2012
Migraine-induced epistaxis and sporadic hemiplegic migraine: unusual features in the same patient.
Journal: Case reports in neurology
Published: July 19, 2012
Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2).
Journal: The journal of headache and pain
Published: March 26, 2012
Sporadic hemiplegic migraine with normal imaging as the initial manifestation of CADASIL.
Journal: Cephalalgia : an international journal of headache
Published: January 18, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026