Results 81 to 90 of about 6,393 (222)

Five Advances in the Last 50 Years That Have Impacted Endocrine Surgery

World Journal of Surgery, EarlyView.
Matilda Anneback, Priya H. Dedhia, Aimee Di Marco, Els Nieveen van Dijkum, Julie A. Miller, Janice L. Pasieka   +5 more
wiley   +1 more source

Patient Characteristics and Clinical Outcomes in a Specialist Hypertension Clinic: A Pragmatic Real‐World Single‐Center Observational Study

The Journal of Clinical Hypertension, Volume 28, Issue 4, April 2026.
ABSTRACT Patients referred to specialist hypertension clinics often have complex disease characterized by secondary causes, treatment resistance and coexisting kidney disease. Real‐world outcome data in this setting remain limited. We conducted a retrospective cohort study of 199 patients attending a tertiary hypertension clinic between January 2017 ...
William R. Marshall, Henry H. L. Wu, Sharmilee Rengarajan, David I. New, Dimitrios Poulikakos, Rajkumar Chinnadurai   +5 more
wiley   +1 more source

Severe Hypertension and Hematologic Abnormalities in Pseudoxanthoma Elasticum: A Pediatric Case Report

The Journal of Clinical Hypertension, Volume 28, Issue 4, April 2026.
ABSTRACT Pseudoxanthoma elasticum (PXE) is a rare autosomal recessive disorder caused by pathogenic variants in ABCC6, leading to progressive calcification of elastic fibers. Although PXE typically presents in adolescence with dermatologic or ocular manifestations, early vascular involvement, including pediatric hypertension, is increasingly recognized.
Hana Flogelova, Dagmar Pospisilova, Lenka Bakaj‐Zbrozkova, Lucie Sochorcova, Jirina Manakova, Eva Kriegova, Pavla Koralkova, Katarina Hlusickova Kapralova, Monika Horvathova   +8 more
wiley   +1 more source

A case of familial phaechromocytoma- was it? [PDF]

, 2015
With advancement in genetic studies, familial phaeochromocytoma (PCC) and paraganglioma (PGL) are increasingly being recognized. Characteristically, correlations exist between genotypes and clinical and biochemical phenotypes.
Mazlan, Khalidah, Umar, Nor Aini, Zahari Sham, Siti Yazmin   +2 more
core  

Management of a pregnant woman with fibromuscular dysplasia [PDF]

, 2018
No abstract ...
Berra, Elena, Bursztyn, Michael, Dominiczak, Anna F., Hammer, Frank, Kahan, Thomas, Micali, Ruben Gabriel, Persu, Alexandre, Pierard, Sophie, Rossi, Gian Paolo, Staessen, Jan A., Touyz, Rhian M.   +10 more
core   +1 more source

Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Pheochromocytoma is a catecholamine‐secreting neuroendocrine tumor originating in the adrenal medulla. In patients with pheochromocytoma, paroxysmal over‐secretion of catecholamines can be triggered by various medications, including the commonly used antiemetic metoclopramide.
Yuki Yamanishi, Kazuki Iio, Keiki Shimizu, Wataru Kasahara, Jun Hamaguchi   +4 more
wiley   +1 more source

Measurement of fractionated plasma metanephrines for exclusion of pheochromocytoma: Can specificity be improved by adjustment for age?

BMC Endocrine Disorders, 2005
Background Biochemical testing for pheochromocytoma by measurement of fractionated plasma metanephrines is limited by false positive rates of up to 18% in people without known genetic predisposition to the disease.
Gafni Amiram, Thabane Lehana, Sawka Anna M, Levine Mitchell, Young William F   +4 more
doaj   +1 more source

Liquid chromatography-tandem mass spectrometry - Application in the clinical laboratory [PDF]

, 2003
This review provides a concise survey of liquid chromatography tandem mass spectrometry (LCTMS) as an emerging technology in clinical chemistry. The combination of two mass spectrometers with an interposed collision cell characterizes LCTMS as an ...
Ford RE, Kushnir MM, Kushnir MM, Muck W, Murdter TE, Rashed MS, Streit F, Taylor RL   +7 more
core   +1 more source

Pheochromocytoma With Langerhans Cell Histiocytosis: A Rare Tumor‐in‐Tumor Case

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Langerhans cell histiocytosis (LCH) occurring in a Pheochromocytoma in the adrenal gland is exceptionally rare and prone to misdiagnosis. The special coexistent tumors harbor distinct genetic mutations. This uncommon case could introduce novel considerations and a strong teaching message to all the clinicians and pathologists.
Cheng Lei, Yulong Guo, Yixin Luo, Qingchun Liang, Jiadi Luo   +4 more
wiley   +1 more source

MON-395 Takotsubo Cardiomyopathy And Metanephrines

Journal of the Endocrine Society, 2019
Takotsubo (stress) cardiomyopathy, is defined by transient left ventricular systolic dysfunction without epicardial coronary disease. Case report A 50-year-old man presented with headache and visual disturbance with no past medical history of note. He had recently separated from his wife and children had moved out of the family home.
Cohen, Pollyanna, Aung, Htet, Rayanagoudar, Girish, Menon, Ravi   +3 more
openaire   +1 more source