Epidemiology of Pheochromocytoma and Paraganglioma: Population-based Cohort Study.
European Journal of Endocrinology, 2020 OBJECTIVE Despite the significant morbidity and mortality associated with pheochromocytoma and paraganglioma, little is known about their epidemiology.
A. Leung +7 more
semanticscholar +1 more source
Integrative multi-omics analysis identifies a prognostic miRNA signature and a targetable miR-21-3p/TSC2/ mTOR axis in metastatic pheochromocytoma/ paraganglioma [PDF]
, 2019 Artículo escrito por un elevado número de autores, solo se referencian el que aparece en primer lugar y los autores pertenecientes a la UAMPheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that present variable outcomes.
Alvarez - Escola, Cristina +1 more
core +2 more sources
Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]
, 2018 Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev +6 more
core +1 more source
Is It a Pheochromocytoma? [PDF]
The Journal of Clinical Hypertension, 2007 The patient is a 44‐year‐old man with a 4‐year history of intermittently elevated blood pressure (BP) controlled by diet and exercise. Three months before evaluation he described daily “spikes” of BP with sharp unilateral headaches. He was seen in the emergency department with a BP of 212/106 mm Hg and was started on hydrochlorothiazide 25 mg daily ...
openaire +3 more sources
Analysis of short-term blood pressure variability in pheochromocytoma/paraganglioma patients [PDF]
, 2019 Data on short-term blood pressure variability (BPV), which is a well-established cardiovascular prognostic tool, in pheochromocytoma and paraganglioma (PPGL) patients is still lack and conflicting.
Bisogni, V. +14 more
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A rare case report of hypertrophic cardiomyopathy induced by catecholamine-producing tumor [PDF]
, 2018 RATIONALE: Catecholamine-producing tumors are rare, occurring in less than 0.2% of patients with hypertension, but can have relevant cardiovascular morbidity and mortality. PATIENT CONCERNS: A 37-year-old woman presented with a history of dyspnea, chest
Bisogni, Valeria +12 more
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α-Toxin permeabilized rat pheochromocytoma cells [PDF]
, 1985 The channel forming α-toxin of Staphylococcus aureus (about 50 μg/ml) markedly reduces the Ca2+ requirement for dopamine release by the rat pheochromocytoma cell line (PC 12).
Baker +12 more
core +1 more source
Computed Tomography Accuracy for Prediction of Adrenal Tumor Adhesion With Organs and Vessels in Dogs and Cats. [PDF]
Vet Radiol UltrasoundABSTRACT The presence of adhesion created by an adrenal tumor (AT) with adjacent structures is important information for surgical planning. We aimed to establish the accuracy of computed tomography (CT) in predicting adrenal tumor adhesion (ATA) with adjacent organs and vessels.
Baldinetti M +10 more
europepmc +2 more sources
Millimolar concentrations of free magnesium enhance exocytosis from permeabilized rat pheochromocytoma (PC 12) cells [PDF]
, 1989 The role of Mg2+ during the final steps of exocytosis was investigated using rat pheochromocytoma cells (PC12) permeabilized with bacterial pore forming toxins.
Ahnert-Hilger +17 more
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Giant cystic pheochromocytoma with low risk of malignancy: A case report and literature teview [PDF]
, 2017 Giant pheochromocytomas are rare silent entities that do not present with the classical symptoms commonly seen in catecholamine-secreting tumors. In many cases they are accidentally discovered.
Baijoo, Shanta +6 more
core +4 more sources