dc.contributor.author | Cetinkaya, Serap | |
dc.contributor.author | Sunamak, Oguzhan | |
dc.contributor.author | Guler, Emel | |
dc.contributor.author | Karabicak, Ilhan | |
dc.contributor.author | Aydogan, Fatih | |
dc.contributor.author | Korman, Mustafa Uğur | |
dc.contributor.author | Aydemir, Ismail | |
dc.date.accessioned | 2021-03-03T07:58:43Z | |
dc.date.available | 2021-03-03T07:58:43Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Sunamak O., Karabicak I., Aydemir I., Aydogan F., Guler E., Cetinkaya S., Korman M. U. , "An intraluminal leiomyoma of the small intestine causing invagination and obstruction: A case report", MOUNT SINAI JOURNAL OF MEDICINE, cilt.73, sa.8, ss.1079-1081, 2006 | |
dc.identifier.issn | 0027-2507 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_14f60d18-93a9-40dc-94f6-e44ea97a9ff8 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/19470 | |
dc.description.abstract | Leiomyomas are mostly of benign character and are rarely seen in the gastrointestinal (GI) system. They represent one subgroup of a group of tumors known as gastrointestinal stromal tumors (GIST). Although rarely seen, they are symptomatic tumors, and they comprise 20-30% of all benign GI tumors. Diagnosis is difficult because of their rarity and the absence of specific symptoms. | |
dc.language.iso | eng | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Temel Tıp Bilimleri | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.title | An intraluminal leiomyoma of the small intestine causing invagination and obstruction: A case report | |
dc.type | Makale | |
dc.relation.journal | MOUNT SINAI JOURNAL OF MEDICINE | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 73 | |
dc.identifier.issue | 8 | |
dc.identifier.startpage | 1079 | |
dc.identifier.endpage | 1081 | |
dc.contributor.firstauthorID | 180578 | |