Results 121 to 130 of about 10,214 (238)

Who can safely discontinue lifelong follow‐up among patients with sporadic pheochromocytoma and paraganglioma?

open access: yesJournal of Internal Medicine, Volume 299, Issue 5, Page 615-627, May 2026.
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

Central Venous Pressure Guided Fluid Management During Anaesthesia of a Phaeochromocytoma Patient with End Stage Renal Disease

open access: yesArchives of Anesthesia and Critical Care, 2017
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]

open access: yes, 2018
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  

Radioiodination of Two Carborane‐Based Dual Cyclooxygenase‐2/5‐Lipoxygenase Inhibitors and Their In Vitro and In Vivo Evaluation

open access: yesChemBioChem, Volume 27, Issue 7, 14 April 2026.
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]

open access: yes, 2011
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  

Phaeochromocytoma [PDF]

open access: yesPostgraduate Medical Journal, 1960
openaire   +2 more sources

Szemfenéki betegségek molekuláris genetikai és epidemiológiai vizsgálata = Molecular genetical and epidemiological investigation of diseases of the ocular fundus [PDF]

open access: yes, 2012
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]

open access: yes, 2016
Adams LG   +19 more
core   +1 more source

Nuclear medicine in endocrine tumours [PDF]

open access: yes, 2011
C
Peremans, Kathelijne   +1 more
core   +2 more sources

Unsuspected phaeochromocytoma [PDF]

open access: yesCanadian Anaesthetists’ Society Journal, 1982
openaire   +2 more sources

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