Results 111 to 120 of about 44,864 (270)

The management of neuroendocrine tumours: A nutritional viewpoint [PDF]

open access: yes, 2017
Nutritional status in patients with neuroendocrine tumours (NETs), especially of gastroenteropancreatic origin, can be deeply affected by excessive production of gastrointestinal hormones, peptides, and amines, which can lead to malabsorption, diarrhoea,
Annamaria Colao   +7 more
core   +1 more source

Effect of salmon calcitonin on symptoms and urinary excretion of 5 hydroxyindoleacetic acid in the carcinoid syndrome. [PDF]

open access: bronze, 1987
Alessandro Antonelli   +4 more
openalex   +1 more source

Carcinoid heart disease – still a challenging diagnosis?

open access: yesRomanian Journal of Cardiology
Neuroendocrine tumors (NETs) are rare neoplasms that can occur anywhere in the body. Mostly, they are located in the gastrointestinal tract or lungs. A third of subjects with NETs present carcinoid syndrome (CS) features.
Benchea Laura Cătălina   +3 more
doaj   +1 more source

Síndrome carcinóide – caso clínico

open access: yesGalicia Clínica, 2017
Os tumores carcinóides são neoplasias raras, mais frequentemente encontradas no trato gastrointestinal, responsáveis pela produção de mediadores neuroendócrinos.
Renata Silva   +3 more
doaj   +1 more source

Meta-analysis of stomatitis in clinical studies of everolimus: incidence and relationship with efficacy. [PDF]

open access: yes, 2016
BackgroundEverolimus, an oral mammalian target of rapamycin (mTOR) inhibitor, is used to treat solid tumors and tuberous sclerosis complex (TSC). Stomatitis, an inflammation of the mucous membranes of the mouth, is a common adverse event associated with ...
Anak, O   +10 more
core  

Carcinoid syndrome [PDF]

open access: yesCanadian Medical Association Journal, 2009
openaire   +3 more sources

Ectopic ACTH syndrome in a dog with a mesenteric neuroendocrine tumour: a case report [PDF]

open access: yes, 2014
Ectopic ACTH secretion is provoked by extra-pituitary tumours that secrete ACTH, constituting an infrequent type of Cushing Syndrome in the dog. Neuroendocrine tumours (NET) are characterised by the synthesis of peptides with hormone activity.
Cabrera Blatter, M. F.   +6 more
core  

Treatment options for PNET liver metastases. a systematic review [PDF]

open access: yes, 2018
Pancreatic neuroendocrine tumors (PNETs) are rare pancreatic neoplasms. About 40-80% of patients with PNET are metastatic at presentation, usually involving the liver (40-93%). Liver metastasis represents the most significant prognostic factor.
Aurello, Paolo   +8 more
core   +1 more source

Cardiac disease and midgut carcinoid syndrome [PDF]

open access: bronze, 2000
G Westberg   +4 more
openalex   +1 more source

Home - About - Disclaimer - Privacy