The pheochromocytoma/paraganglioma syndrome: an overview on mechanisms, diagnosis and management
JV Lima, CE Kater - International braz j urol, 2023 - SciELO Brasil
Pheochromocytomas/paragangliomas (PPGL) are rare, metastatic, and potentially fatal
neuroendocrine tumors, often neglected because they present symptoms similar to other …
neuroendocrine tumors, often neglected because they present symptoms similar to other …
Lutathera® Orphans: State of the Art and Future Application of Radioligand Therapy with 177Lu-DOTATATE
Lutathera® is the first EMA-and FDA-approved radiopharmaceutical for radioligand therapy
(RLT). Currently, on the legacy of the NETTER1 trial, only adult patients with progressive …
(RLT). Currently, on the legacy of the NETTER1 trial, only adult patients with progressive …
Genetics of pheochromocytomas and paragangliomas determine the therapeutical approach
Pheochromocytomas and paragangliomas are the most heritable endocrine tumors. In
addition to the inherited mutation other driver mutations have also been identified in tumor …
addition to the inherited mutation other driver mutations have also been identified in tumor …
Pheochromocytoma: a changing perspective and current concepts
A Kiriakopoulos, P Giannakis… - … in endocrinology and …, 2023 - journals.sagepub.com
This article aims to review current concepts in diagnosing and managing
pheochromocytoma and paraganglioma (PPGL). Personalized genetic testing is vital, as 40 …
pheochromocytoma and paraganglioma (PPGL). Personalized genetic testing is vital, as 40 …
Reduction in CgA-Derived CST Protein Level in HTR-8/SVneo and BeWo Trophoblastic Cell Lines Caused by the Preeclamptic Environment
M Bralewska, T Pietrucha, A Sakowicz - International Journal of …, 2023 - mdpi.com
One of the most dangerous complications of pregnancy is preeclampsia (PE), a disease
associated with a high risk of maternal and fetal mortality and morbidity. Although its etiology …
associated with a high risk of maternal and fetal mortality and morbidity. Although its etiology …
Risk factors for intraoperative complications in pheochromocytomas
M Araujo-Castro, RG Centeno… - Endocrine-related …, 2021 - erc.bioscientifica.com
We aimed to identify presurgical and surgical risk factors for intraoperative complications in
patients with pheochromocytomas. A retrospective study of patients with …
patients with pheochromocytomas. A retrospective study of patients with …
[HTML][HTML] Surgical strategies of complicated pheochromocytomas/paragangliomas and literature review
X Wang, Y Zhao, Z Liao, Y Zhang - Frontiers in Endocrinology, 2023 - frontiersin.org
Pheochromocytomas (PCC)/paragangliomas (PGL) are catecholamine (CA)-secreting
neuroendocrine tumors, which are known as PPGL due to their histological and …
neuroendocrine tumors, which are known as PPGL due to their histological and …
The role of VHL in the development of Von Hippel-Lindau Disease and Erythrocytosis
P Hudler, M Urbancic - Genes, 2022 - mdpi.com
Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem
neoplastic syndrome stemming from germline disease-associated variants of the VHL tumor …
neoplastic syndrome stemming from germline disease-associated variants of the VHL tumor …
[HTML][HTML] Immunohistochemical expression of choline acetyltransferase and catecholamine-synthesizing enzymes in head-and-neck and thoracoabdominal …
N Kimura, K Shiga, K Kaneko, Y Oki, C Sugisawa… - Endocrine …, 2021 - Springer
Paragangliomas (PGLs) are neural-crest-derived, non-epithelial neuroendocrine tumors
distributed along the parasympathetic and sympathetic nerves. Head-and-neck PGLs …
distributed along the parasympathetic and sympathetic nerves. Head-and-neck PGLs …
[PDF][PDF] 嗜铬细胞瘤诊断研究进展
侯倩， 张彪， 罗瑶， 尚攀峰 - 临床泌尿外科杂志, 2022 - lcmwen.whuhzzs.com
嗜铬细胞瘤诊断研究进展∗ Page 1 临床泌尿外科杂志 2022年 JClinUrology(China) 37卷12期
引用本文:侯倩,张彪,罗瑶,等.嗜铬细胞瘤诊断研究进展[J].临床泌尿外科杂志,2022,37(12):946-951.DOI …
引用本文:侯倩,张彪,罗瑶,等.嗜铬细胞瘤诊断研究进展[J].临床泌尿外科杂志,2022,37(12):946-951.DOI …