dc.contributor.author | Ozdemir, Nuriye Guzin | |
dc.contributor.author | Batur, Sebnem | |
dc.contributor.author | Atci, Burak | |
dc.contributor.author | Kocak, Ayhan | |
dc.contributor.author | Turk, Okan | |
dc.contributor.author | Yaldiz, Can | |
dc.contributor.author | Antar, Veysel | |
dc.contributor.author | Demirel, Nail | |
dc.date.accessioned | 2021-03-04T08:59:54Z | |
dc.date.available | 2021-03-04T08:59:54Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Turk O., Yaldiz C., Antar V., Batur S., Demirel N., Atci B., Ozdemir N. G. , Kocak A., "Spinal paragangliomas Surgical treatment and follow-up outcomes in eight cases", MEDICINE, cilt.97, sa.38, 2018 | |
dc.identifier.issn | 0025-7974 | |
dc.identifier.other | av_6628a391-18a6-4c31-b2cd-4e1eeb31e499 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/70958 | |
dc.identifier.uri | https://doi.org/10.1097/md.0000000000012468 | |
dc.description.abstract | Paragangliomas are neuro-endocrine tumors originating from the adrenal gland. They are usually benign and nonfunctioning, rarely seen in central nervous system. More than 90% of central nervous system paragangliomas are manifested as carotid and glomus jugulare tumors. Spinal paragangliomas are quite rare. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp | |
dc.subject | Temel Tıp Bilimleri | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.title | Spinal paragangliomas Surgical treatment and follow-up outcomes in eight cases | |
dc.type | Makale | |
dc.relation.journal | MEDICINE | |
dc.contributor.department | Sakarya Training & Research Hospital , , | |
dc.identifier.volume | 97 | |
dc.identifier.issue | 38 | |
dc.contributor.firstauthorID | 256122 | |