http://www.cnr.it/ontology/cnr/individuo/prodotto/ID26723
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses (Articolo in rivista)
- Type
- Label
- ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s10072-008-0870-0 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Cologno D.; d'Onofrio F.; Esposito T.; Gianfrancesco F.; Petretta V.; Casucci G.; Frediani F.; Buzzi M.G.; Bussone G. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Azienda Ospedaliero-Universitaria Ospedali Riuniti, Institute of Clinical Neurophysiology, Department of Neuroscience Foggia, Italy;
Institute of Neurology \"San G. Moscati\" Hospital Avellino, Italy;
Institute of Genetics and Biophysics Italian National Research Council Naples, Italy;
Casa di Cura \"S. Francesco\" Telese (BN), Italy;
Institute of Neurology Ponte S. Pietro (Bergamo), Italy;
IRCCS Santa Lucia Foundation Rome, Italy;
Institute of Neurology, IRCCS \"C. Besta\" Milan, Italy; (literal)
- Titolo
- ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses (literal)
- Abstract
- Basilar-type migraine (BM) and hemiplegic migraine are clinically distinct subtypes of migraine with aura, however they do share clinical features and it is possible they may share genetic bases. In recent years, ATP1A2 and other gene mutations have been discovered in familial and sporadic hemiplegic migraine. More recently, an ATP1A2 mutation has been identified in an Italian family with BM. In this study we document the absence of ATP1A2 mutations in two Italian sisters with menstrual BM, suggesting that other genes are involved in the condition. (literal)
- Prodotto di
- Autore CNR
- Insieme di parole chiave
Incoming links:
- Autore CNR di
- Prodotto
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- Insieme di parole chiave di