Results 91 to 100 of about 45,090 (245)

Bilateral papillopathy as a presenting sign of pheochromocytoma associated with von Hippel–Lindau disease

open access: yes, 2014
Veeral Shah, Leonid Zlotcavitch, Angela M Herro, Sander R Dubovy, Zohar Yehoshua, Byron L LamBascom Palmer Eye Institute, University of Miami, Miller School of Medicine, Miami, FL, USAAbstract: A 7-year-old girl presented with decreased vision in both ...
Herro AM   +5 more
core  

Biochemical Diagnosis and Localization of Pheochromocytoma [PDF]

open access: yes, 2006
Pheochromocytomas can have a highly variable presentation, making diagnosis challenging. To think of the tumor represents the crucial initial step, but establishing the diagnosis requires biochemical evidence of excessive catecholamine production and ...
Lenders, Jacques W. M.   +34 more
core   +1 more source

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

Pheochromocytoma and paraganglioma

open access: yesAnales del Sistema Sanitario de Navarra, 2009
Pheochromocytoma and paraganglioma are neoplasias of the chromaffin cells that manifest themselves in some 40-60% of cases by symptoms of episodic freeing of catecholamines. They are the cause of stable and malign HTA in some 0.1-1% of cases and must be discounted in a study of the same.
M E, Petrina   +2 more
openaire   +3 more sources

Pheochromocytoma [PDF]

open access: yesArchives of Surgery, 1972
S, Warren, R N, Chute
openaire   +4 more sources

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

open access: yes
World Journal of Surgery, EarlyView.
Matilda Anneback   +5 more
wiley   +1 more source

Cancer heterogeneity explored through immune cell deconvolution of the tumor microenvironment

open access: yesQuantitative Biology, Volume 14, Issue 3, September 2026.
Abstract Cancer is a highly heterogeneous disease, characterized by significant variability across multiple dimensions. This diversity has been extensively studied from various perspectives. In this study, we aim to examine cancer heterogeneity through the lens of immune cell composition within the tumor microenvironment.
Limin Jiang   +4 more
wiley   +1 more source

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

open access: yesPediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski   +9 more
wiley   +1 more source

A Prospective Evaluation of Glucagon Stimulation Test Safety in Adults With Chronic Moderate‐to‐Severe Traumatic Brain Injury

open access: yesEndocrinology, Diabetes &Metabolism, Volume 9, Issue 4, July 2026.
The glucagon stimulation test demonstrates a favourable safety profile in adults with chronic moderate‐to‐severe traumatic brain injury, with transient, non‐severe adverse effects and no serious complications. ABSTRACT Introduction Growth hormone deficiency (GHD) is a common and clinically significant consequence of moderate‐to‐severe traumatic brain ...
Corey Snyder   +2 more
wiley   +1 more source

Composite pheochromocytoma with a malignant peripheral nerve sheath tumor: Case report and review of the literature

open access: yesAsian Journal of Surgery, 2016
Adrenal tumors with more than one cellular component are uncommon. Furthermore, an adrenal tumor composed of a pheochromocytoma and a malignant peripheral nerve sheath tumor is extremely rare.
Takeshi Namekawa   +9 more
doaj   +1 more source

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