Results 51 to 60 of about 6,550 (210)
Post-Transcriptional Dysregulation by miRNAs Is Implicated in the Pathogenesis of Gastrointestinal Stromal Tumor [GIST] [PDF]
, 2013 peer-reviewedIn contrast to adult mutant gastrointestinal stromal tumors [GISTs], pediatric/wild-type GISTs remain poorly understood overall, given their lack of oncogenic activating tyrosine kinase mutations.
Hans-Ulrich Schildhaus +12 more
core +5 more sources
Utility of immunohistochemical staining for the diagnosis of Extra-adrenal mediastinal paraganglioma
Respiratory Medicine Case Reports, 2020 Extra-adrenal, mediastinal paraganglioma are rare tumors that origin from sympathetic ganglia. Common diagnostic steps include CT, MRI and PET-Scan.
Isabella B. Metelmann +3 more
doaj +1 more source
Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors [PDF]
, 2014 Peer ...
Arola, Johanna +9 more
core +1 more source
Case Reports in Endocrinology, 2012 A 30-year-old woman with severe hypertension was admitted to the hospital with a history of headache, palpitations, and diaphoresis following sexual intercourse.
Nicola Di Daniele +7 more
doaj +1 more source
Coexistence of pheochromocytoma/praganglioma and renal artery stenosis
Indian Journal of Endocrinology and Metabolism, 2012 Renal artery stenosis (RAS) often coexists with pheochromocytoma (Pheo)/paraganglioma (PGL) and often alters the management of patients with Pheo/PGL. We have studied the prevalence of RAS in our Pheo/PGL patients.
Vijaya Sarathi +6 more
doaj +1 more source
Pancreatic paraganglioma mimicking pancreatic neuroendocrine tumor
Rare Tumors, 2020 Extra-adrenal paragangliomas are rare tumors arising from the chromaffin cells of the autonomic nervous system. Retroperitoneal paragangliomas may present as a pancreatic mass.
Arezou Abbasi +2 more
doaj +1 more source
Clinical and prognostic implications of the genetic diagnosis of hereditary NET syndromes in asymptomatic patients [PDF]
, 2011 Neuroendocrine tumors (NETs) can be sporadic or they can arise in complex hereditary syndromes. Patients with hereditary NETs can be identified before the development of tumors by performing genetic screenings.
COLAO, ANNAMARIA +9 more
core +1 more source
Paraganglioma of the Spermatic Cord: Case Report and Review of the Literature [PDF]
, 2008 Paragangliomas rarely involve the genitourinary tract. We present a case of a paraganglioma arising from the spermatic cord and review the literature on the ...
Freeman, A +6 more
core +3 more sources
Carney triad. Report of one case [PDF]
, 2017 Indexación: Scopus.Carney described a disorder characterized by the presence of several uncommon tumors which were pulmonary chondromas, gastric sarcomas and extra-adrenal paragangliomas.
Lovera Riquelme, C. +4 more
core +1 more source
Urology Annals, 2010 Object: The purpose was to highlight the diagnosis and treatment of extra-adrenal para-gangliomas, which often causes catecholamine hypersecretion and hypertension.
Wen Jin +5 more
doaj