Searchable abstracts of presentations at key conferences in endocrinology

Endocrine Abstracts

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ea0062wh7 | Workshop H: Miscellaneous endocrine and metabolic disorders | EU2019

A case of cocaine-induced acute symptomatic hyponatraemia

McDonald Basil , Walton Matthew , Idowu Oluwagbemiga , Barratt Jon , Vakilgilani Tannaz

A 34-year old lady with a history of Crohn’s colitis and depression presented to the Emergency Department (ED) reporting an allergic reaction to azathioprine. She complained of mild headache, anxiety and nausea but denied wheeze, shortness of breath, tongue swelling or rash. Her medications were prednisolone, predfoam enemas, escitalopram, combined oral contraceptive pill (OCP) and azathioprine, commenced one month ago. She denied alcohol or recreational drug consumption....
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ea0050p243 | Neoplasia, Cancer and Late Effects | SFEBES2017

Analysis of the diagnosis, treatment and genetics of 175 cases of phaeochromocytoma and paraganglioma in two ENETS Centres of Excellence

Stoenchev Kostadin , McDonald Basil , Dean Sophie , Canham Natalie , Palazzo Fausto , Banga Neal , Clarke Peter , Harcourt Jonathan , Baker Darryl , Todd Jeannie , Martin Niamh , Wernig Florian , Chahal Harvinder , Sam Amir , Hatfield Emma , Dhillo Waljit , Meeran Karim , Grossman Ashley , Toumpanakis Christos , Caplin Martyn , Tan Tricia , Khoo Bernard

Background: Phaeochromocytomas (PCC) and paragangliomas (PGL) are tumours derived from neural crest cells within the adrenal medulla or extra-adrenal ganglia, respectively. Over 20 known genes are implicated in at least 30% of cases. Experience with these tumours in individual centres is limited due to their rarity.Objective: To describe the demographics, genetics, treatment and progression-free survival (PFS) in ...
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ea0050p243 | Neoplasia, Cancer and Late Effects | SFEBES2017

Analysis of the diagnosis, treatment and genetics of 175 cases of phaeochromocytoma and paraganglioma in two ENETS Centres of Excellence

Stoenchev Kostadin , McDonald Basil , Dean Sophie , Canham Natalie , Palazzo Fausto , Banga Neal , Clarke Peter , Harcourt Jonathan , Baker Darryl , Todd Jeannie , Martin Niamh , Wernig Florian , Chahal Harvinder , Sam Amir , Hatfield Emma , Dhillo Waljit , Meeran Karim , Grossman Ashley , Toumpanakis Christos , Caplin Martyn , Tan Tricia , Khoo Bernard

Background: Phaeochromocytomas (PCC) and paragangliomas (PGL) are tumours derived from neural crest cells within the adrenal medulla or extra-adrenal ganglia, respectively. Over 20 known genes are implicated in at least 30% of cases. Experience with these tumours in individual centres is limited due to their rarity.Objective: To describe the demographics, genetics, treatment and progression-free survival (PFS) in ...
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Endocrine Abstracts
ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
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