Somatic VHLgene alterations in MEN2-associated medullary thyroid carcinoma (2006)
Koch, Christian A, Brouwers, Frederieke M, Vortmeyer, Alexander O, Tannapfel, Andrea, Libutti, Steven K, Zhuang, Zhengping, ...
Abstract Background Germline mutations in RET are responsible for multiple endocrine neoplasia type 2 (MEN2), an autosomal dominantly inherited cancer syndrome that is characterized by medullary...
Radiofrequency Ablation: a Novel Approach for Treatment of Metastatic Pheochromocytoma (2001)
Pacak, Karel, Fojo, Tito, Goldstein, David S., Eisenhofer, Graeme, Walther, McClellan M., Linehan, W. Marston, ...
Yu, Shuhua, Gavrilova, Oksana, Chen, Hui, Lee, Randy, Liu, Jie, Pacak, Karel, ...
Heterozygous disruption of Gnas, the gene encoding the stimulatory G-protein α subunit (Gsα), leads to distinct phenotypes depending on whether the maternal (m–/+) or paternal (+/p–) allele is...
Somatic VHL gene alterations in MEN2-associated medullary thyroid carcinoma
Koch, Christian A, Brouwers, Frederieke M, Vortmeyer, Alexander O, Tannapfel, Andrea, Libutti, Steven K, Zhuang, Zhengping, ...
Yu, Shuhua, Gavrilova, Oksana, Chen, Hui, Lee, Randy, Liu, Jie, Pacak, Karel, ...
Heterozygous disruption of Gnas, the gene encoding the stimulatory G-protein α subunit (Gsα), leads to distinct phenotypes depending on whether the maternal (m–/+) or paternal (+/p–) allele is...
Somatic VHL gene alterations in MEN2-associated medullary thyroid carcinoma
Koch, Christian A, Brouwers, Frederieke M, Vortmeyer, Alexander O, Tannapfel, Andrea, Libutti, Steven K, Zhuang, Zhengping, ...
Eisenhofer, Graeme, Huynh, Thanh-Truc, Elkahloun, Abdel, Morris, John C., Bratslavsky, Gennady, Linehan, W. Marston, ...
Pheochromocytomas in patients with von Hippel-Lindau (VHL) syndrome and multiple endocrine neoplasia type 2 (MEN 2) differ in the types and amounts of catecholamines produced and the resulting signs...