Molecular defects causing ovarian dysfunction

dc.contributor.authorKalantaridou, S. N.en
dc.contributor.authorChrousos, G. P.en
dc.date.accessioned2015-11-24T19:04:05Z
dc.date.available2015-11-24T19:04:05Z
dc.identifier.issn0077-8923-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19968
dc.rightsDefault Licence-
dc.subjectAromatase/metabolismen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectHypogonadism/genetics/metabolismen
dc.subjectLuteinizing Hormone/genetics/physiologyen
dc.subjectMaleen
dc.subjectMutationen
dc.subjectOvarian Diseases/*geneticsen
dc.subjectPrimary Ovarian Insufficiency/geneticsen
dc.subjectPuberty, Delayed/geneticsen
dc.subjectPuberty, Precocious/geneticsen
dc.titleMolecular defects causing ovarian dysfunctionen
heal.abstractThe functions of the hypothalamic-pituitary-ovarian and -adrenal axes are intertwined, and molecular defects in either axis may cause ovarian dysfunction. Advances in molecular genetics have allowed new insights into the pathophysiology of ovarian disorders. Specific gene mutations causing delayed puberty and/or ovarian failure, and heterosexual or isosexual precocious puberty have recently been described. The molecular insights gained into ovarian dysfunction have already led to rational therapies for some of these conditions.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/10818390-
heal.journalNameAnn N Y Acad Scien
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2000-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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