Results 121 to 130 of about 10,214 (238)
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
A 42-year-old male with a 2-year history on dialysis for renal failure was admitted for adrenalectomy. We applied central venous catheter for this phaeochromocytoma case before the induction of anaesthesia.
Mohammadreza Kamranmanesh +3 more
doaj
123I-Methyljodbenzylguanidin- (MIBG-) Szintigraphie: Paradoxe Nuklidspeicherung eines onkozytären Nebennierenrindenkarzinoms [PDF]
Zusammenfassung: Das mit Radiojod markierte Katecholaminanalogon Methyljodbenzylguanidin (MIBG) eignet sich aufgrund seiner selektiven Aufnahme in chromaffine Gewebe in hervorragender Weise für die bildgebende Diagnostik des Phäochromozytoms und besitzt ...
Padberg, B.-C +5 more
core
Two dicarbadodecaborane(12)‐based dual cyclooxygenase‐2/5‐lipoxygenase (COX‐2/5‐LO) inhibitors were 123I‐labeled. Refinement of labeling and formulation conditions and extensive in vitro characterization are presented. Cell uptake studies in COX‐2‐ and 5‐LO‐overexpressing cell lines showed COX‐2‐independent and partly 5‐LO‐dependent uptake.
Jonas Schädlich +11 more
wiley +1 more source
Phaeochromocytoma Associated to Von Recklinghausen Neurofibromatosis Type I: a Rare Clinical Case [PDF]
Os feocromocitomas são neoplasias originárias das células cromafins da crista neural localizados, na sua grande maioria, na medula supra-renal, podendo também aparecer nos gânglios simpáticos (paragangliomas).
Jorge, V +4 more
core
Szemfenéki betegségek molekuláris genetikai és epidemiológiai vizsgálata = Molecular genetical and epidemiological investigation of diseases of the ocular fundus [PDF]
Genetikai eset-kontroll tanulmányunkba 213 nedves és 67 száraz AMD-ben szenvedő beteget, valamint 106 kontrolt vontunk be. Nem találtunk összefüggést az AMS és 4 vizsgált gén között (Apolipoprotein E, complement factor I, FXIII and MerTK).
Balogh, István +4 more
core
ISFM Consensus Guidelines on the Diagnosis and Management of Feline Chronic Kidney Disease [PDF]
Adams LG +19 more
core +1 more source
Nuclear medicine in endocrine tumours [PDF]
C
Peremans, Kathelijne +1 more
core +2 more sources
Unsuspected phaeochromocytoma [PDF]
openaire +2 more sources

