Results 181 to 190 of about 50,666 (222)
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Biochemical Assessment of Pheochromocytoma and Paraganglioma.
Endocrine reviews, 2023Pheochromocytoma and paraganglioma (PPGL) require prompt consideration and efficient diagnosis and treatment to minimize associated morbidity and mortality. Once considered, appropriate biochemical testing is key to diagnosis.
G. Eisenhofer, C. Pamporaki, J. Lenders
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Genetic bases of pheochromocytoma and paraganglioma.
Journal of Molecular Endocrinology, 2022The genetics of pheochromocytoma and paraganglioma (PPGL) has become increasingly complex over the last two decades. The list of genes involved in the development of these tumors has grown steadily, and there are currently more than 20 driver genes ...
A. Cascón +6 more
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Pancreas, 2021
This manuscript is the result of the North American Neuroendocrine Tumor Society consensus conference on the medical management and surveillance of metastatic and unresectable pheochromocytoma and paraganglioma held on October 2 and 3, 2019.
Lauren Fishbein +17 more
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This manuscript is the result of the North American Neuroendocrine Tumor Society consensus conference on the medical management and surveillance of metastatic and unresectable pheochromocytoma and paraganglioma held on October 2 and 3, 2019.
Lauren Fishbein +17 more
semanticscholar +1 more source
Current Opinion in Otolaryngology & Head & Neck Surgery, 2023
Purpose of review A vagal paraganglioma is a rare head and neck tumor arising from the paraganglionic tissue within the perineurium of the vagus nerve, anywhere along the course of the nerve. Due to its proximity to the internal carotid artery, the internal jugular vein and the lower cranial nerves, this disorder poses ...
Lena, Mottie +2 more
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Purpose of review A vagal paraganglioma is a rare head and neck tumor arising from the paraganglionic tissue within the perineurium of the vagus nerve, anywhere along the course of the nerve. Due to its proximity to the internal carotid artery, the internal jugular vein and the lower cranial nerves, this disorder poses ...
Lena, Mottie +2 more
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Journal of Craniofacial Surgery, 2019
Background: Paragangliomas are groups of neuroendocrine neoplasms originating from neural crest cells throughout the body, but are rarely observed within the orbit. Case report: Two patients, a 4-year-old male and 27-year-old female, presented with a slow-growing proptosis.
Binbin, Zhu, Jianhua, Yan
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Background: Paragangliomas are groups of neuroendocrine neoplasms originating from neural crest cells throughout the body, but are rarely observed within the orbit. Case report: Two patients, a 4-year-old male and 27-year-old female, presented with a slow-growing proptosis.
Binbin, Zhu, Jianhua, Yan
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Pheochromocytoma and Paraganglioma.
New England Journal of Medicine, 2019Pheochromocytoma and Paraganglioma Pheochromocytoma and paraganglioma are related tumors that differ mainly in location; pheochromocytomas are adrenal, and paragangliomas can be anywhere else.
H. Neumann, W. Young, C. Eng
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European Archives of Oto-Rhino-Laryngology, 2007
Temporal paragangliomas (PGL) are usually limited to the paraganglionar system with a sporadic or familial origin. Familial PGL have recently been shown to be associated with germline alterations in SDH group of genes, and occasionally are associated with a variety of genetic multisystemic disorders (von Hippel-Lindau disease, multiple endocrine ...
Carlos, Suárez +2 more
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Temporal paragangliomas (PGL) are usually limited to the paraganglionar system with a sporadic or familial origin. Familial PGL have recently been shown to be associated with germline alterations in SDH group of genes, and occasionally are associated with a variety of genetic multisystemic disorders (von Hippel-Lindau disease, multiple endocrine ...
Carlos, Suárez +2 more
openaire +2 more sources