Octreotide use for rescue of vision in a pregnant patient with acromegaly

Autor: Anne Marie Hannon, Isolda Frizelle, George Kaar, Steven J Hunter, Mark Sherlock, Christopher J Thompson, Domhnall J O’Halloran

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)

Pregnancy in acromegaly is rare and generally safe, but tumour expansion may occur. Managing tumour expansion during pregnancy is complex, due to the potential complications of surgery and side effects of anti-tumoural medication. A 32-year-old woman

Externí odkaz: https://doaj.org/article/3d0e02c10dce4cc0932167a490d1c1b3

Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours

Autor: Paul Benjamin Loughrey, Federico Roncaroli, Estelle Healy, Philip Weir, Madhu Basetti, Ruth T Casey, Steven J Hunter, Márta Korbonits

Publikováno v: Loughrey, P B, Roncaroli, F, Healy, E, Weir, P, Basetti, M, Casey, R T, Hunter, S J & Korbonits, M 2022, ' Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours ', Endocrine-Related Cancer, vol. 29, no. 10, R157–R172 . https://doi.org/10.1530/ERC-22-0157

Pituitary neuroendocrine tumours (PitNETs) associated with paragangliomas or phaeochromocytomas are rare. SDHx variants are estimated to be associated with 0.3–1.8% of PitNETs. Only a few case reports have documented the association with MAX varian

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6bbc7e47fe087b5ab4d2da328db6ca7
https://pure.qub.ac.uk/en/publications/ef522843-c1ed-4903-94da-307f09de37d6

Central diabetes insipidus from a patient's perspective: management, psychological co-morbidities, and renaming of the condition: results from an international web-based survey

Autor: Cihan Atila, Paul Benjamin Loughrey, Aoife Garrahy, Bettina Winzeler, Julie Refardt, Patricia Gildroy, Malak Hamza, Aparna Pal, Joseph G Verbalis, Christopher J Thompson, Lars G Hemkens, Steven J Hunter, Mark Sherlock, Miles J Levy, Niki Karavitaki, John Newell-Price, John A H Wass, Mirjam Christ-Crain

Publikováno v: The lancet. Diabetesendocrinology. 10(10)

Background\ud \ud Central diabetes insipidus is a rare neuroendocrine condition. Data on treatment-associated side-effects, psychological comorbidities, and incorrect management are scarce. The aim of this study was to investigate patients’ perspec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89dc26a8faea9a58cb3df7d1f7a9b9d3
https://pubmed.ncbi.nlm.nih.gov/36007537

Pituitary surgery in northern ireland: A twenty year retrospective population based analysis

Autor: Eileen Parkes, Jacqueline James, Stephanie G Craig, Márta Korbonits, Debarata Bhattacharya, Steven J. Hunter, Brian Herron, Paul Benjamin Loughrey, Stephen Cooke, Manuel Salto-Tellez, Philip Weir, Darragh G. McArt, Erin Sturdy

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0272ee819a134d33457fb3b1d46a2d7d
https://doi.org/10.1530/endoabs.73.aep488

Clinical features and autoimmune associations in patients presenting with Idiopathic Isolated ACTH deficiency

Autor: Domhnall J O'Halloran, Anne Marie Hannon, Steven J. Hunter, Christopher J. Thompson, Mark Sherlock, Diarmuid Smith

Publikováno v: Clinical Endocrinology. 88:491-497

Objective Idiopathic Isolated ATCH deficiency (IIAD) is a rare cause of secondary adrenal insufficiency. As the condition is rare, and the diagnostic criteria ill-defined, there are few good clinical descriptions in the literature. We have described

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7bc48e958497c2c23a28792410543e3
https://doi.org/10.1111/cen.13536