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Publications by Raquel G. Gouveia

Recurrent ATP1A2 Mutations in Portuguese Families With Familial Hemiplegic Migraine

Journal of Human Genetics

English

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Sporadic Hemiplegic Migraine With ATP1A2 and Prothrombin Gene Mutations

Case Reports in Neurological Medicine

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The Contribution of CACNA1A, ATP1A2 and SCN1A Mutations in Hemiplegic Migraine: A Clinical and Genetic Study in Finnish Migraine Families

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Familial Hemiplegic Migraine With Prolonged Hemiplegia

Archives of Disease in Childhood

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Divergent Sodium Channel Defects in Familial Hemiplegic Migraine

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

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Familial Hemiplegic Migraine Type I: The Molecular Signaling Pathway

Journal of Neurology & Stroke

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Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Cav2.1 Ca2+Channel Gating

Journal of Biological Chemistry

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Respiratory Arrest in Familial Hemiplegic Migraine: A Clinical and Neuropathological Study.

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

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Sporadic Hemiplegic Migraine and CREST Syndrome

Journal of Headache and Pain

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