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Infertility treatment in autosomal dominant polycystic kidney disease (ADPKD) - a case report

dc.contributor.authorOnur, R
dc.contributor.authorKadioglu, A
dc.contributor.authorErgin, E
dc.contributor.authorKoksal, IT
dc.contributor.authorOrhan, I
dc.date.accessioned2021-03-05T17:10:07Z
dc.date.available2021-03-05T17:10:07Z
dc.date.issued2000
dc.identifier.citationOrhan I., Onur R., Ergin E., Koksal I., Kadioglu A., "Infertility treatment in autosomal dominant polycystic kidney disease (ADPKD) - a case report", ANDROLOGIA, cilt.32, ss.91-93, 2000
dc.identifier.issn0303-4569
dc.identifier.otherav_c43930ad-3490-4196-bc75-0b1fcaaa819c
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/130148
dc.identifier.urihttps://doi.org/10.1046/j.1439-0272.2000.00335.x
dc.description.abstractAutosomal dominant polycystic kidney disease (ADPKD) is a frequently occurring inherited condition with cysts in many organs including the kidneys. However, a combination of seminal vesicle cysts, cystic obstruction of ejaculatory duct and ADPKD is rarely encountered. The following case report presents an infertile ADPKD patient who had seminal vesicle cysts and ejaculatory duct cyst, and describes the treatment by transurethral resection of the ejaculatory duct.
dc.language.isoeng
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectTıp
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectANDROLOJİ
dc.titleInfertility treatment in autosomal dominant polycystic kidney disease (ADPKD) - a case report
dc.typeMakale
dc.relation.journalANDROLOGIA
dc.contributor.department, ,
dc.identifier.volume32
dc.identifier.issue2
dc.identifier.startpage91
dc.identifier.endpage93
dc.contributor.firstauthorID125293


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