Results 111 to 120 of about 711,467 (262)

Correlation of Matrix Metalloproteinases and Tissue Inhibitors of Matrix Metalloproteinase Expression in Ileal Carcinoids, Lymph Nodes and Liver Metastasis with Prognosis and Survival [PDF]

open access: yes, 2009
Purpose: Ileal carcinoids are gut epithelial tumors originating from serotonin-containing enterochromaffin (EC) cells. Therapeutic options for effectively inhibiting the growth and spread of metastatic carcinoids are still limited.
Baur, Dorothee M.   +8 more
core   +2 more sources

Impact on symptoms and survival of bone metastases in patients with small‐intestinal neuroendocrine tumours

open access: yesJournal of Neuroendocrinology, Volume 37, Issue 10, October 2025.
Abstract We aimed to assess the symptoms and impact on overall survival (OS) from bone metastases (BM) diagnosed on Gallium‐68‐labelled DOTA tyrosine octreotide positron emission tomography with computed tomography (68Ga‐DOTATOC‐PET/CT) in patients with well‐differentiated small intestinal neuroendocrine tumours (Si‐NETs).
Maria Wedin   +4 more
wiley   +1 more source

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

Unresectable Primary Enteric‐Type Thymic Adenocarcinoma Treated With FOLFOX Chemotherapy: A Case Report

open access: yesCancer Reports, Volume 8, Issue 9, September 2025.
ABSTRACT Background Enteric‐type thymic adenocarcinomas are an extremely rare and distinct subtype of thymic malignancies, as classified by the 2021 World Health Organization classification of thymic tumors. These tumors exhibit close molecular and morphologic similarity to primary gastrointestinal malignancies. To date, there are no tailored treatment
Carl He   +3 more
wiley   +1 more source

Rare Case of Neuroendocrine Metastasis to the Left Ventricle

open access: yesJACC: Case Reports
Carcinoid syndrome is a constellation of signs and symptoms caused by different hormones produced by carcinoid tumors. Very rarely, those tumors can metastasize to the heart and cause cardiac involvement of the tumor. This study presents a very rare case
Said Hajouli, MD   +7 more
doaj   +1 more source

Carcinoid Heart Disease: A Rare Cause of Right Ventricular Dysfunction Evaluation by Transthoracic 2D, Doppler and 3-D Echocardiography [PDF]

open access: yes, 2011
Carcinoid heart disease is a rare cause of heart failure with or without right valvular heart impairments. In this study, we showed a case of carcinoid tumour with hepatic metastases inducing carcinoid heart disease.
Arcangelo Midolla   +16 more
core   +2 more sources

Epithelial–Mesenchymal Transition in Cancer: Insights Into Therapeutic Targets and Clinical Implications

open access: yesMedComm, Volume 6, Issue 9, September 2025.
This graphical abstract summarizes the effects of ionizing radiation (IR) on epithelial–mesenchymal transition (EMT), emphasizing critical processes such as DNA damage repair, tumor microenvironment interactions, and resistance mechanisms. It highlights EMT‐induced radioresistance regulators, such as TGF‐β, Wnt, Notch, ERK, and various miRNAs, as well ...
Dhasarathdev Srinivasan   +7 more
wiley   +1 more source

Echocardiographic imaging of tricuspid and pulmonary valve abnormalities in primary ovarian carcinoid tumor

open access: yesCardiovascular Ultrasound, 2010
Carcinoid is a rare malignancy originating from enterochromaffin cells and is clinically characterized by flushing, diarrhea and bronchospasm, due to secretion of vasoactive substances.
Aggeli Constantina   +6 more
doaj   +1 more source

Focal Spot, Summer 2002 [PDF]

open access: yes, 2002
https://digitalcommons.wustl.edu/focal_spot_archives/1091/thumbnail ...

core   +1 more source

Small bowel neuroendocrine tumors: from pathophysiology to clinical approach [PDF]

open access: yes, 2016
Neuroendocrine tumors (NETs), defined as epithelial tumors with predominant neuroendocrine differentiation, are among the most frequent types of small bowel neoplasm.
Cotter, José   +2 more
core   +1 more source

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