The blind-ending bifid ureter

dc.contributor.authorGiannakopoulos, X.en
dc.contributor.authorChambilomatis, P.en
dc.contributor.authorThirothoulakis, M.en
dc.contributor.authorSeferiadis, G.en
dc.date.accessioned2015-11-24T19:42:23Z
dc.date.available2015-11-24T19:42:23Z
dc.identifier.issn0301-1623-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/24634
dc.rightsDefault Licence-
dc.subjectAdulten
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectPyelonephritis/*etiologyen
dc.subjectUreter/*abnormalities/surgeryen
dc.subjectUreteral Obstruction/*etiologyen
dc.titleThe blind-ending bifid ureteren
heal.abstractA bifid blind-ending ureter is an extremely rare congenital anomaly of the upper urinary tract. This unusual ureteric condition appears to be more common in female subjects. Such patients may be asymptomatic or present with recurrent urinary tract infections, frequency, nycturia, abdominal pain or calculi. Asymptomatic patients without urinary tract infection require no treatment. When symptoms or infection are present, the treatment is surgical excision of the blind branch with antireflux reimplantation of the normal ureter. If hydronephrosis, pyonephrosis or renal damage is present, nephroureterectomy may be required.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8034425-
heal.journalNameInt Urol Nephrolen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1994-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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