Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Domhnall J. O'Halloran"'
Autor:
Mairead T. Crowley, Eibhlin Lonergan, Peter O’Callaghan, Caroline M. Joyce, M. Morita, Niamh Conlon, Domhnall J. O’Halloran
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background Non-islet cell tumour hypoglycemia (NICTH) is rarely encountered in clinical practice. Insulin-like growth factor 2 (IGF2) is the most common cause of NICTH observed in the setting of mesenchymal and epithelial neoplasia. This is
Externí odkaz:
https://doaj.org/article/7090ece49449403ab5894ea7c3c0bf91
Autor:
Caroline M. Joyce, Jayne A. Houghton, Domhnall J. O’Halloran, Paula M. O’Shea, Susan M. O’Connell
Publikováno v:
Clinical Case Reports, Vol 8, Iss 7, Pp 1217-1222 (2020)
Abstract Advances in genomics and 18F‐DOPA PET‐CT imaging have transformed the management of infants with Congenital Hyperinsulinism. Preoperative diagnosis of focal hyperinsulinism permits limited pancreatectomy with improved clinical outcomes w
Externí odkaz:
https://doaj.org/article/93c48b1e28ea4ca3ad300815f61d5e6f
Autor:
Susan M. O’Connell, Jayne A L Houghton, Paula M O'Shea, Domhnall J O'Halloran, Caroline Joyce
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 7, Pp 1217-1222 (2020)
Clinical Case Reports, Vol 8, Iss 7, Pp 1217-1222 (2020)
Advances in genomics and 18F‐DOPA PET‐CT imaging have transformed the management of infants with Congenital Hyperinsulinism. Preoperative diagnosis of focal hyperinsulinism permits limited pancreatectomy with improved clinical outcomes while know
Autor:
Mairead T. Crowley, Eibhlin Lonergan, Peter O’Callaghan, Caroline M. Joyce, M. Morita, Niamh Conlon, Domhnall J. O’Halloran
Publikováno v:
BMC endocrine disorders. 22(1)
Background Non-islet cell tumour hypoglycemia (NICTH) is rarely encountered in clinical practice. Insulin-like growth factor 2 (IGF2) is the most common cause of NICTH observed in the setting of mesenchymal and epithelial neoplasia. This is a paraneo
Autor:
Anne Marie Hannon, Aftab Khattak, Mark J Hannon, James Gibney, Domhnall J O'Halloran, Claire A. Thompson, Rosemary Dineen, Triona O'Shea, Mark Sherlock, Christopher J. Thompson, Steven J. Hunter
Publikováno v:
European Journal of Endocrinology. 180:K21-K29
Pregnancy is rarely reported in acromegaly. Many patients are diagnosed in later life and younger patients may have subfertility due to hypopituitarism. We present a case series of 17 pregnancies in 12 women with acromegaly. Twelve women with acromeg
Autor:
Fidelma Dunne, E. Brosnan, Aoife M. Egan, M Durkan, A Khamis, P Ferry, Graham A Roberts, M Todd, W.A. Wan Mahmood, Liam O'Mahony, Breda Kirwan, M. Fenlon, E. O'Sullivan, Andrew Smyth, Louise Carmody, M Peter, M S Murphy, S Hoashi, L. Culliney, O. Yousif, Marc Nolan, Antoinette Tuthill, H. Clarke, M.J. Brassill, T. Higgins, G. Hanlon, Domhnall J O'Halloran, C. Coogan Kelly, C. McGurk, B Kinsley, Aaron Liew, T Kinsley, P. Murphy, C McHugh
Publikováno v:
Diabetic Medicine. 37:2044-2049
Aims The purpose of this study was to identify the number of pregnancies affected by pre-gestational diabetes in the Republic of Ireland; to report on pregnancy outcomes and to identify areas for improvement in care delivery and clinical outcomes. Me
Publikováno v:
Diabetes. 70
Corticosteroid-induced hyperglycaemia (CIH) is commonly encountered among acute respiratory inpatients, particularly those with diabetes mellitus (DM). Guidelines dictate frequency of inpatient capillary blood glucose (CBG) monitoring and treatment m
Publikováno v:
Biochemia Medica
Volume 30
Issue 2
Volume 30
Issue 2
Plasma free metanephrines or urinary fractionated metanephrines are the biochemical tests of choice for the diagnosis of pheochromocytoma as they have greater sensitivity and specificity than catecholamines for pheochromocytoma detection. This case h
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
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
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)
Summary 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-o