Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/86355
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dc.contributor.authorAgius, Maria Petra-
dc.contributor.authorCamilleri, Lianne-
dc.contributor.authorGruppetta, Mark-
dc.contributor.authorVassallo, Josanne-
dc.date.accessioned2022-01-04T13:28:57Z-
dc.date.available2022-01-04T13:28:57Z-
dc.date.issued2019-03-
dc.identifier.citationAgius, M. P., Camilleri, L., Gruppetta, M., & Vassallo, J. (2019). Isolate hypogonadotropic hypogonadism : a review in a Maltese cohort. European Journal of Obstetrics & Gynecology and Reproductive Biology, 234, e144.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/86355-
dc.description.abstractIsolated hypogonadotropic hypogonadism (IHH) is a rare genetic disorder of isolated GnRH deficiency, characterised by varying degrees of disruption in sexual maturation. When associated with anosmia, it is termed Kallmann's Syndrome.en_GB
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectHypogonadism -- Maltaen_GB
dc.subjectKallmann Syndromeen_GB
dc.titleIsolate hypogonadotropic hypogonadism : a review in a Maltese cohorten_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1016/j.ejogrb.2018.08.475-
dc.publication.titleEuropean Journal of Obstetrics & Gynecology and Reproductive Biologyen_GB
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