Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura, differentiated only by motor symptoms, which are absent in BM. Mutations in CACNA1A and ATP1A2 have been found in FHM. The authors detected a novel mutation in the ATP1A2 gene (R548H) in members of a family with BM, suggesting that BM and FHM may be allelic disorders.

Familiar basilar migraine associated with a new mutation in the ATP1A2 gene / Ambrosini, A; D'Onofrio, M; Grieco, Gs; DI MAMBRO, A; Montagna, G; Fortini, D; Nicoletti, Ferdinando; Nappi, Giuseppe; Sancesc, G; Schoenen, J; Buzzi, Mg; Santorelli, Fm; Pierelli, Francesco. - In: NEUROLOGY. - ISSN 0028-3878. - STAMPA. - 65(11):(2005), pp. 1826-1828. [10.1212/01.wnl.0000187072.71931.c0]

Familiar basilar migraine associated with a new mutation in the ATP1A2 gene

NICOLETTI, Ferdinando;NAPPI, Giuseppe;PIERELLI, Francesco
2005

Abstract

Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura, differentiated only by motor symptoms, which are absent in BM. Mutations in CACNA1A and ATP1A2 have been found in FHM. The authors detected a novel mutation in the ATP1A2 gene (R548H) in members of a family with BM, suggesting that BM and FHM may be allelic disorders.
2005
Basilar migraine; new mutation; ATP1A2 gene
01 Pubblicazione su rivista::01a Articolo in rivista
Familiar basilar migraine associated with a new mutation in the ATP1A2 gene / Ambrosini, A; D'Onofrio, M; Grieco, Gs; DI MAMBRO, A; Montagna, G; Fortini, D; Nicoletti, Ferdinando; Nappi, Giuseppe; Sancesc, G; Schoenen, J; Buzzi, Mg; Santorelli, Fm; Pierelli, Francesco. - In: NEUROLOGY. - ISSN 0028-3878. - STAMPA. - 65(11):(2005), pp. 1826-1828. [10.1212/01.wnl.0000187072.71931.c0]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/235860
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