Results 111 to 120 of about 34,897 (270)

Non-functional paraganglioma of the urinary bladder: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction Paragangliomas that originate from the urinary bladder are extremely rare. In most series, bladder paragangliomas often cause micturitional attacks.
Gao Yi   +4 more
doaj   +1 more source

Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report [PDF]

open access: yes, 2017
BackgroundRecent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes.
Adachi Yayoi   +13 more
core   +2 more sources

Paraganglioma de mediastino com metástases pulmonares Pulmonary metastasis of mediastinal paraganglioma

open access: yesJornal Brasileiro de Pneumologia, 2005
Descrevemos uma paciente de 27 anos que se apresentou com paraganglioma de mediastino anterior e médio e nódulos pulmonares bilaterais. O tratamento consistiu na ressecção das lesões pulmonares através de toracotomia anterior bilateral transesternal e ...
Manoel Ximenes Netto   +4 more
doaj   +1 more source

A Paraganglioma in a Hypertensive Patient with Unilateral Renal Hypoplasia [PDF]

open access: yes, 2015
We report the case of a 46-year-old hypertensive Japanese female with renal insufficiency related to unilateral renal hypoplasia. The patient was found to have developed paraganglioma in the retroperitoneal space over a 5-year period.
Hagiya, Hideharu   +9 more
core   +1 more source

Paraganglioma laríngeo

open access: yes, 2013
Os Paragangliomas são tumores do sistema neuroendócrino, com uma incidência rara na cabeça e pescoço. Na laringe estão identificadas três localizações distintas, sendo a mais frequente a região supraglótica. São considerados tumores benignos, sem capacidade de metastização, contudo o diagnostico diferencial com outras lesões neuroendócrinas é ...
Freitas, Luís   +5 more
openaire   +2 more sources

The role of complex II in disease [PDF]

open access: yes, 2012
Genetically defined mitochondrial deficiencies that result in the loss of complex II function lead to a range of clinical conditions. An array of tumor syndromes caused by complex II-associated gene mutations, in both succinate dehydrogenase and ...
Alston   +96 more
core   +1 more source

Jugular Foramen Syndrome: Concurrent Neurological Deficits, Advanced Imaging Findings, Underlying Diagnoses, and Outcomes in 14 Dogs (2016–2024)

open access: yesJournal of Veterinary Internal Medicine, Volume 39, Issue 3, May/June 2025.
ABSTRACT Background Jugular foramen syndrome (JFS), dysfunction of cranial nerves (CNs) IX, X, and XI caused by lesions involving the jugular foramen (JF), is rarely reported in dogs. Objective Describe presenting complaints, neurologic findings, advanced imaging findings, underlying diagnoses, and outcomes in dogs with JFS.
Megan Madden   +7 more
wiley   +1 more source

Hypertension secondary to paraganglioma: case report and review of the literature

open access: yesIatreia, 2016
We report the case of a 25 year-old man with a history of transient stroke during adolescence, and longstanding uncontrolled hypertension who presented with palpitations, diaphoresis and headache.
Rubio-Marín, Andrea Constanza   +3 more
doaj   +1 more source

Mutated TP53 is a marker of increased VEGF expression: analysis of 7,525 pan-cancer tissues. [PDF]

open access: yes, 2020
Anti-angiogenic therapies are an important class of anti-cancer treatment drugs. However, their efficacy is limited to certain tumors and would benefit from identifying a biomarker predictive of therapeutic response.
Boichard, Amélie   +2 more
core  

A case of carotid body paraganglioma and haemangioblastoma of the spinal cord in a patient with the N131K missense mutation in the VHL gene [PDF]

open access: yes, 2011
The article describes paraganglioma case in woman with von Hippel–Lindau disease. She was found to be a carrier of a rare germline mutation in the VHL gene (393C>A; N131K).
Barbara Bobek-Billewicz   +24 more
core   +2 more sources

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