Results 101 to 110 of about 6,958 (252)

The value of plasma metanephrine measurements during adrenal vein sampling

open access: yesEndocrine Connections
Objective: The assessment of primary aldosteronism incorporates adrenal vein sampling (AVS) to lateralize aldosterone excess. Current adrenal vein sampling protocols rely on concurrent cortisol measurements to assess successful cannulation and ...
Richard W Carroll   +9 more
doaj   +1 more source

Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation

open access: yesCase Reports in Endocrinology, 2018
Background. Pheochromocytoma/paraganglioma is a rare tumor from neuroendocrine cells. 1/3rd of cases have germline mutations. Papillary thyroid carcinoma (PTC) is a common neoplasm from follicular cells of the thyroid.
Lorena Rasquin   +3 more
doaj   +1 more source

Corticosterone Potentiation of Cocaine-Induced Reinstatement of Conditioned Place Preference in Mice is Mediated by Blockade of the Organic Cation Transporter 3 [PDF]

open access: yes, 2016
The mechanisms by which stressful life events increase the risk of relapse in recovering cocaine addicts are not well understood. We previously reported that stress, via elevated corticosterone, potentiates cocaine-primed reinstatement of cocaine seeking
A Amphoux   +51 more
core   +2 more sources

Resistant arterial hypertension in a patient with adrenal incidentaloma multiple steno-obstructive vascular lesions and antiphospholipid syndrome [PDF]

open access: yes, 2015
Resistant hypertension is defined as above of blood pressure (≤ 140/90 mmHg) despite therapy with three or more antihypertensive drugs of different classes at maximum tolerable doses with one bling a diuretic.
CONCISTRE, ANTONIO   +8 more
core  

Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease. [PDF]

open access: yes, 1996
Inherited pheochromocytomas are often part of familial syndromes, especially multiple endocrine neoplasia type 2 (MEN 2), retinal cerebellar hemangioblastomatosis [von Hippel-Lindau (vHL) disease] or neurofibromatosis type 1.
Crossey, P.A.   +7 more
core   +1 more source

Comprehensive personalized approach to the diagnosis and treatment of pheochromocytoma and paraganglioma

open access: yesУкраїнський журнал клінічної хірургії
Objective. To evaluate the effectiveness of a comprehensive approach to the diagnosis and treatment of pheochromocytoma and paraganglioma with a special focus on the role of selective venous blood sampling, X–ray endovascular selective electrocoagulation
O. M. Simonov   +6 more
doaj   +1 more source

Use of new biochemical plasmatic markers, plasma free and total metanephrines, for the diagnosis and follow-up of neuroblastoma in children with clinical correlation [PDF]

open access: yes, 2012
Background: Neuroblastoma is a paediatrictumour derived from the neural crest. Biochemical diagnosis and follow up rely on quantitation of urinary catecholamines (dopamine and noradrenaline) and their metabolites vanillylmandelic acid (VMA) and ...
Jobe, Ch.
core  

Predicting Hemodynamic Fluctuations During Adrenalectomy for Pheochromocytoma

open access: yesDiagnostics
Background: Pheochromocytoma is a rare adrenal neuroendocrine tumor characterized by excessive catecholamine secretion, which can lead to significant perioperative hemodynamic instability.
Marina Stojanovic   +8 more
doaj   +1 more source

The role of metanephrines in the diagnosis of pheochromocytoma [PDF]

open access: bronze, 2021
Emad Rezkallah   +2 more
openalex   +1 more source

The value of plasma markers for the clinical behaviour of phaeochromocytomas [PDF]

open access: yes, 2002
OBJECTIVE: Phaeochromocytomas (PCCs) are widely known for their clinical unpredictability. This study intends to define predictive plasma markers for their variable postoperative behaviour.
Bonjer, H.J. (Jaap)   +8 more
core  

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