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2009 NOV 16 ... included. The final diagnosis was pheochromocytoma in 40, adrenal hyperplasia in two, paraganglioma in two, ganglioneuroma in one, and unknown in three. Sensitivities and discordancy ...
2009 SEP 29 ... Keywords: New Zealand, Auckland, Angiology, Biopsy, Laryngology, Otology, Paraganglioma, Reoperation, Surgery. This article was prepared by Life Science Weekly ...
2009 OCT 26 ... accounting for <0.5% of all tumors; and they are the most common extra-adrenal paraganglioma. In this study, CBTs were clinically suspected in 31 patients but diagnosed by ...
2009 NOV 2 ... Catheterization, Common Carotid Artery, Embolization, Neoplasms, Neuroradiology, Paraganglioma, Radiology, Surgery. This article was prepared by Hematology Week editors ...
2009 NOV 30 ... human adrenal medullas, two of three human pheochromocytomas, and one extra-adrenal paraganglioma showed RET induction corresponding with extensive nerve growth factor-induced outgrowth ...
2009 SEP 21 ... "Germline mutations in SDHx genes cause hereditary paraganglioma. The aim of the study was to assess the indications for succinate dehydrogenase (SDH) ...
2009 NOV 16 ... paraganglionic tissue. There are very few case reports on primary pulmonary paraganglioma in the literature," scientists writing in the journal Thoracic and Cardiovascular ...
2009 DEC 1 ... to a study from Madrid, Spain, "Hereditary susceptibility to pheochromocytoma (PCC) and paraganglioma (PGL) represents a very complex genetic scenario. It has been reported that the absence ...
2009 OCT 12 ... "Paragangliomas may have composite forms in which they combine features of a typical paraganglioma with those of a neural component consisting of either neuroblastoma, ...
2009 SEP 28 ... gene, located on chromosome 11q13.1, segregate with disease in a family with hereditary paraganglioma, a neuroendocrine tumor previously linked to mutations in genes encoding SDH subunits," ...
2009 SEP 14 ... "Preoperative arterial embolization (AE) of paraganglioma (PG) is widely used to diminish intraoperative blood loss. Thereby conditions for a ...
2009 SEP 14 ... "Mutations in SDHB are one of the causes of hereditary paraganglioma syndrome. Germline mutations in SDHB predispose to the development of head and neck ...
2009 OCT 12 ... ([I-131] MIBG) in the treatment of malignant pheochromocytoma (PHEO) and paraganglioma (PGL). Fifty patients with metastatic PHEO or PGL, age 10 to 64 years, were treated with ...
2009 SEP 21 ... "Up to one third of all symptomatic presentations of pheochromocytoma or paraganglioma are due to germline mutations in one of six genes defining multiple endocrine neoplasia ...
2009 OCT 5 ... radiation dosimetry, and clinical safety in 11 patients with confirmed pheochromocytoma/paraganglioma (Pheo) or carcinoid tumors. A single 5.0-mCi (185 MBq) injection of Ultratrace ...
2009 SEP 14 ... paraganglia. The identification of mutations in one of the several pheochromocytoma/paraganglioma susceptibility genes may indicate a specific clinical management drive. Less well ...
2009 SEP 21 ... of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients,' are detailed in a study published in Endocrine-related Cancer. "A major ...
2009 NOV 30 ... in a 60-year-old woman with widespread hepatic metastases from a malignant paraganglioma. Temozolomide was orally administered in daily doses of 250 mg on days 1 to 5 and ...
2009 NOV 23 ... we present a 35-year-old white man with primary malignant abdominal extra-adrenal 11 cm paraganglioma underwent surgical successful resection. But 6 months later, he developed extensive ...
