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dc.contributor.authorDaniel, E
dc.contributor.authorDebono, M
dc.contributor.authorCaunt, S
dc.contributor.authorGirio-Fragkoulakis, C
dc.contributor.authorWalters, S
dc.contributor.authorAkker, S
dc.contributor.authorGrossman, A
dc.contributor.authorTrainer, Peter J
dc.contributor.authorNewell-Price, J
dc.date.accessioned2018-02-12T14:12:43Z
dc.date.available2018-02-12T14:12:43Z
dc.date.issued2018-01-08
dc.identifier.citationA prospective longitudinal study of Pasireotide in Nelson's syndrome. 2018 Pituitaryen
dc.identifier.issn1573-7403
dc.identifier.pmid29313180
dc.identifier.doi10.1007/s11102-017-0853-3
dc.identifier.urihttp://hdl.handle.net/10541/620821
dc.description.abstractNelson's syndrome is a challenging condition that can develop following bilateral adrenalectomy for Cushing's disease, with high circulating ACTH levels, pigmentation and an invasive pituitary tumor. There is no established medical therapy. The aim of the study was to assess the effects of pasireotide on plasma ACTH and tumor volume in Nelson's syndrome.
dc.language.isoenen
dc.rightsArchived with thanks to Pituitaryen
dc.titleA prospective longitudinal study of Pasireotide in Nelson's syndrome.en
dc.typeArticleen
dc.contributor.departmentDepartment of Oncology and Metabolism, The Medical School, University of Sheffield, Beech Hill Road, Sheffield, S10 2RX, UKen
dc.identifier.journalPituitaryen
refterms.dateFOA2018-12-17T15:13:48Z
html.description.abstractNelson's syndrome is a challenging condition that can develop following bilateral adrenalectomy for Cushing's disease, with high circulating ACTH levels, pigmentation and an invasive pituitary tumor. There is no established medical therapy. The aim of the study was to assess the effects of pasireotide on plasma ACTH and tumor volume in Nelson's syndrome.


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