Results 61 to 70 of about 6,393 (222)

Persistent Erythrocytosis in a Dog With a Spinal Sclerosing Paraganglioma

open access: yesVeterinary Clinical Pathology, EarlyView.
ABSTRACT A 7‐year‐old, male, castrated, mixed‐breed dog presented with right pelvic limb lameness and pain on posturing to defecate that began 1.5 years prior to presentation. Radiographs taken 8 months prior to presentation showed a small lytic lesion of the L6 vertebral body, and CBCs showed a persistently increased hematocrit (HCT) for at least 2 ...
Samuel V. Neal   +11 more
wiley   +1 more source

Modified Pisano Method for Estimating Urinary Metanephrines

open access: yesClinical Chemistry, 1973
Abstract The Pisano method [Clin. Chim. Acta 5, 406 (1960)] for estimating urinary metanephrine, used in the screening of hypertensive persons for pheochromocytoma, has been modified by replacing ion-exchange chromatography with differential solvent extraction.
R N, Gupta, D, Price, P M, Keane
openaire   +2 more sources

Adrenal Hypertension: Aspects of Laboratory Examination

open access: yesMìžnarodnij Endokrinologìčnij Žurnal, 2015
The need for a correct choice of managing patients with hypertension is due to the possible development of heart failure and cardiovascular complications.
L.A. Lutsenko
doaj   +1 more source

Implementation of First‐Line Rapid Genome Sequencing for Children in Pediatric and Cardiac Intensive Care Units

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1326-1336, June 2026.
ABSTRACT Substantial data supports the use of rapid exome and genome sequencing (rES/rGS) in Neonatal Intensive Care Units (NICU), but fewer studies have examined the impact of rES/rGS in other pediatric critical care units. We evaluated the impact on diagnostic yield and time to diagnosis following a single‐center hospital policy change allowing ...
Alexandra C. Keefe   +22 more
wiley   +1 more source

Update on Modern Management of Pheochromocytoma and Paraganglioma [PDF]

open access: yesEndocrinology and Metabolism, 2017
Despite all technical progress in modern diagnostic methods and treatment modalities of pheochromocytoma/paraganglioma, early consideration of the presence of these tumors remains the pivotal link towards the best possible outcome for patients.
Jacques W. M. Lenders, Graeme Eisenhofer
doaj   +1 more source

悪性褐色細胞腫患者の生存と化学療法の効果 [PDF]

open access: yes, 2009
2850285
Bravo   +20 more
core   +2 more sources

A Biochemically “Silent” Aortocaval Paraganglioma in a 19‐Year‐Old Female Causing Intraoperative Hypertensive Crisis: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Paragangliomas may appear biochemically silent, yet still behave as functional tumors with severe intraoperative consequences. Normal preoperative catecholamine screening does not exclude the risk of hypertensive crisis during surgery.
Abdul Basit   +5 more
wiley   +1 more source

Pheochromocytoma arising from an ectopic adrenal tissue in multiple endocrine neoplasia type 2A

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2019
A 21-year-old woman was referred to our hospital to treat bilateral pheochromocytomas (PCCs) after a diagnosis of multiple endocrine neoplasia type 2A (MEN2A). We performed bilateral laparoscopic adrenalectomy.
Haruyuki Ohsugi   +3 more
doaj   +1 more source

Disease-modifying polymorphisms and C609Y mutation of RET associated with high penetrance of phaeochromocytoma and low rate of MTC in MEN2A. [PDF]

open access: yes, 2016
Mutations of the rearranged during transfection (RET) proto-oncogene, located on chromosome 10q11.2, cause multiple endocrine neoplasia type 2A (MEN2A).
Calva   +9 more
core   +3 more sources

Who can safely discontinue lifelong follow‐up among patients with sporadic pheochromocytoma and paraganglioma?

open access: yesJournal of Internal Medicine, Volume 299, Issue 5, Page 615-627, May 2026.
Abstract Background Current guidelines recommend at least 10 years of follow‐up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high‐risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow‐up are scarce. Methods Among 999 patients with PPGL, 703 who were non‐metastatic,
Min Jeong Park   +15 more
wiley   +1 more source

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