dc.contributor.author | ULUKAN, Çağrı | |
dc.contributor.author | Aydin, Nursel | |
dc.contributor.author | ERDOĞAN, SEYDA | |
dc.contributor.author | PEKER, ELİF | |
dc.contributor.author | Tezcan, Sabiha | |
dc.date.accessioned | 2022-02-18T09:30:01Z | |
dc.date.available | 2022-02-18T09:30:01Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Tezcan S., ULUKAN Ç., ERDOĞAN S., PEKER E., Aydin N., "Two Cases of Dyke-Davidoff Masson Syndrome", EPILEPSI, cilt.23, sa.3, ss.131-134, 2017 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_419fe341-761f-4c0f-99cb-e14d14bed2b7 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/177341 | |
dc.identifier.uri | https://doi.org/10.14744/epilepsi.2017.03016 | |
dc.description.abstract | Dyke-Davidoff Masson Syndrome (DDMS) is a rare syndrome characterized by seizures, facial asymmetry, and contralateral hemiplegia or hemiparesis. The typical radiological features of DDMS include cerebral hemiatrophy with ipsilateral hypertrophy of the skull and sinuses. It is usually diagnosed in childhood. Presently described are 2 rare cases of DDMS that were diagnosed in adults based on magnetic resonance imaging of the brain. | |
dc.language.iso | eng | |
dc.subject | Neurology | |
dc.subject | Neurology (clinical) | |
dc.subject | Life Sciences | |
dc.subject | Health Sciences | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Nöroloji | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | KLİNİK NEUROLOJİ | |
dc.title | Two Cases of Dyke-Davidoff Masson Syndrome | |
dc.type | Makale | |
dc.relation.journal | EPILEPSI | |
dc.contributor.department | Ankara Üniversitesi , , | |
dc.identifier.volume | 23 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 131 | |
dc.identifier.endpage | 134 | |
dc.contributor.firstauthorID | 3385117 | |