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dc.contributor.authorSarimurat, N
dc.contributor.authorYEKER, Daver
dc.contributor.authorKARA, C
dc.contributor.authorSENYUZ, Osman Faruk
dc.contributor.authorCelayir, S
dc.contributor.authorILCE, Z
dc.contributor.authorERDOGAN, E
dc.date.accessioned2021-03-03T13:59:45Z
dc.date.available2021-03-03T13:59:45Z
dc.date.issued2003
dc.identifier.citationILCE Z., ERDOGAN E., KARA C., Celayir S., Sarimurat N., SENYUZ O. F. , YEKER D., "Pyloric atresia: 15-year review from a single institution", JOURNAL OF PEDIATRIC SURGERY, cilt.38, sa.11, ss.1581-1584, 2003
dc.identifier.issn0022-3468
dc.identifier.otherav_373869fc-e0a0-425a-84a0-db69ce14fbad
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/41249
dc.identifier.urihttps://doi.org/10.1016/s0022-3468(03)00565-7
dc.description.abstractBackground: Pyloric atresia (PA) is a rare pathology. Calder presented the first pyloric atresia case in 1749 and Touroff, Sussman, Meltz, and their colleagues presented the first successful operation in 1940. PA has 3 types of anatomic variations: (1) type A, pyloric membrane or web; (2) type B, the pyloric channel is a solid cord; and (3) type C, in which there is a gap between the stomach and duodenum. Associated anomalies also have been described. Epidermolysis bullosa (EB) and intestinal anomalies occur most often with this condition.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titlePyloric atresia: 15-year review from a single institution
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC SURGERY
dc.contributor.department, ,
dc.identifier.volume38
dc.identifier.issue11
dc.identifier.startpage1581
dc.identifier.endpage1584
dc.contributor.firstauthorID31482


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