Zobrazeno 1 - 10
of 1 515
pro vyhledávání: '"phaeochromocytoma"'
Autor:
Morgane Gavet, Stephane Junot
Publikováno v:
Open Veterinary Journal, Vol 14, Iss 6, Pp 1483-1490 (2024)
Background: The anaesthetic management of adrenalectomies for phaeochromocytoma excision, a catecholamine secreting tumour, is challenging due to the potential for fatal complications following severe haemodynamic variations, including hypertensive c
Externí odkaz:
https://doaj.org/article/4b5be091d0f1472e9b7b5fdc23fa63ef
Autor:
Prodromos Chatzikyriakou, Dimitria Brempou, Mark Quinn, Lauren Fishbein, Roberta Noberini, Ioannis N. Anastopoulos, Nicola Tufton, Eugenie S. Lim, Rupert Obholzer, Johnathan G. Hubbard, Mufaddal Moonim, Tiziana Bonaldi, Katherine L. Nathanson, Louise Izatt, Rebecca J. Oakey
Publikováno v:
Clinical Epigenetics, Vol 15, Iss 1, Pp 1-16 (2023)
Abstract Background Phaeochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumours. Pathogenic variants have been identified in more than 15 susceptibility genes; associated tumours are grouped into three Clusters, reinforced by their
Externí odkaz:
https://doaj.org/article/66cb18fe933b4376a23415ba736e406b
Autor:
Jasmijn B. Miltenburg, Marnix Gorissen, Inge van Outersterp, Iris Versteeg, Alex Nowak, Richard J. Rodenburg, Antonius E. van Herwaarden, Andre J. Olthaar, Benno Kusters, Catleen Conrad, Henri J. L. M. Timmers, Margo Dona
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 7262 (2024)
Phaeochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumours arising from chromaffin cells. Pathogenic variants in the gene succinate dehydrogenase subunit B (SDHB) are associated with malignancy and poor prognosis. When metastases a
Externí odkaz:
https://doaj.org/article/961dca1808a84ff68bb172692136b4bd
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Ibom Medical Journal, Vol 16, Iss 3 (2023)
Phaeochromocytoma is a tumour from chromaffin cells in adrenal medulla or extra-adrenal autonomic ganglia, usually releasing catecholamines and metanephrines. It is an unusual cause of severe hypertension in the young. This is the first report from o
Externí odkaz:
https://doaj.org/article/27298814721e4d359f8f973c9114c1c8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Christopher S. Boot
Publikováno v:
Diagnostics, Vol 13, Iss 18, p 2940 (2023)
Phaeochromocytomas (PC) and sympathetic paragangliomas (PGL) are potentially malignant tumours arising from the adrenal medulla (PC) or elsewhere in the sympathetic nervous system (PGL). These tumours usually secrete catecholamines and are associated
Externí odkaz:
https://doaj.org/article/cff605d3d838404c9f590c7f4c013ca1
Autor:
Maryam Ranjbar, Ahmad Amin, Ziae Totonchi, Zahra Ghaemmaghami, Zahra Jalilian, Mahshid Hesami, Nader Givtaj, Amir Nasser Jadbabaei, Iman Divanbeigi, Mohammad Mohsen Mazloomfard
Publikováno v:
ESC Heart Failure, Vol 9, Iss 1, Pp 213-218 (2022)
Abstract Phaeochromocytomas/paragangliomas (PPGL) are rare tumours that can cause cardiovascular complications following the secretion of catecholamines. We present a young female presented with heart failure with reduced ejection fraction as a resul
Externí odkaz:
https://doaj.org/article/4a8daae818014805b25255311667b6b3
Tumour detection and outcomes of surveillance screening in SDHB and SDHD pathogenic variant carriers
Autor:
Gemma White, Anand Velusamy, Samantha Anandappa, Michael Masucci, Louise A Breen, Mamta Joshi, Barbara McGowan, Johnathan G H Hubbard, Rupert Obholzer, Dimitra Christodoulou, Audrey Jacques, Philip Touska, Fahim-Ul Hassan, Louise Izatt, Paul V Carroll
Publikováno v:
Endocrine Connections, Vol 11, Iss 2, Pp 1-8 (2022)
Objective: Succinate dehydrogenase subunit (SDHx) pathogenic variants predispose to phaeochromocytoma and paraganglioma (PPGL). Lifelong surveillance is recommended for all patients to enable prompt detection and treatment. There is currently limited
Externí odkaz:
https://doaj.org/article/36c51d78b84d4c5b98d2abfda8669ee6