Results 81 to 90 of about 5,463 (222)
ChemBioChem, Volume 27, Issue 1, January 2026.Radiopharmaceuticals enable precise cancer diagnosis and targeted therapy by combining radioactive isotopes with carrier molecules. This review summarizes advances from 2014 to 2025, emphasizing probe design, click chemistry, novel targets, and nanodelivery systems.
Mohd Sayeed Shaikh +7 more
wiley +1 more source
Pheochromocytoma and Diffuse Large B‐Cell Lymphoma in the Ipsilateral Adrenal Gland: A Case Report
IJU Case Reports, Volume 9, Issue 1, January 2026.ABSTRACT Introduction Pheochromocytoma is a catecholamine‐producing tumor arising from the adrenal medulla. When it coexists with a tumor of different origin within the same adrenal gland, it is classified as a collision tumor involving a pheochromocytoma.
Ken Maekawa +9 more
wiley +1 more source
Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report [PDF]
, 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
Medicinal Research Reviews, Volume 46, Issue 1, Page 203-237, January 2026.ABSTRACT Targeted radioligand therapy has emerged as a promising treatment option for eradicating advanced cancer forms. α‐Emitters are considered particularly promising as they can obliterate (micro)‐metastases. The α‐emitter astatine‐211 (211At) has experienced increased interest due to its favorable decay properties.
Marius Müller +5 more
wiley +1 more source
BMJ Mental HealthBackground It has been reported that patients with geriatric psychiatric disorders include many cases of the prodromal stages of neurodegenerative diseases.
Masaki Fujiwara +7 more
doaj +1 more source
Frontiers in Oncology, 2019 Background: Pheochromocytoma and paraganglioma (PHEO/PGL) are rare neuroendocrine tumors which may cause potentially life-threatening complications, with about a third of cases found to harbor specific gene mutations.
Abhishek Jha +26 more
doaj +1 more source
The neuronal imaging in cardiology: 123I-mIBG in clinical practice
Biophysical ReviewsNeuronal imaging, or assessment of sympathetic activity of the heart, along with the study of perfusion, myocardial and coronary blood flow reserve, and contractility, is another unique facet of nuclear medicine and an integral component in unravelling and understanding the mechanisms of cardiovascular disease (CVD) development, predicting the course ...
L. E. Samoilenko +2 more
openaire +2 more sources
Renal 123I-MIBG Scintigraphy Before and After Kidney Autotransplantation
Clinical Nuclear Medicine, 2015 A 25-year-old man underwent an autotransplantation of his right kidney because of fibromuscular dysplasia-induced renal artery stenosis and subsequent hypertension. Since transplantation results in complete kidney denervation, it enabled assessment of renal sympathetic nerve activity changes using renal I-MIBG scintigraphy.
Dobrowolski, Linn C. +4 more
openaire +3 more sources
Journal of Neuroendocrinology, Volume 38, Issue 1, January 2026.Abstract Early detection of metastases and timely surgical intervention play a crucial role in the management of neuroendocrine tumors. In large‐sized pheochromocytomas and sympathetic paragangliomas (PPGL), functional imaging with positron emission tomography (PET) is recommended, as it improves the detection of metastases, which may go undetected on ...
Achyut Ram Vyakaranam +8 more
wiley +1 more source
Adrenal pheochromocytoma incidentally discovered in a patient with parkinsonism [PDF]
, 2015 To evaluate the diagnostic route of pheochromocytoma (PHEO) in a patient under dopaminergic treatment. A 70-year-old man with Parkinsonism and under treatment with levodopa and carbidopa came to our observation for evaluation of arterial hypertension and
Claudio Letizia +7 more
core +1 more source