HuGE Literature Finder
Records
1
-
7
Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
Genetic Characteristics of Incidental Pheochromocytoma and Paraganglioma. The Journal of clinical endocrinology and metabolism 2022 Feb . Zhang Jing, Li Minghao, Pang Yingxian, Wang Cikui, Wu Jingjing, Cheng Ziyun, Li Xiaomu, Lu Zhiqiang, Liu Yujun, Guo Jianming, Chen Xiang, He Yao, Guan Xiao, Xu Xiaowen, Wang Yong, Liu Jiahao, Guo Wei, Hou Yingyong, Liu Longfei, Jiang Jingjing, Gao X |
Somatic IDH1 hotspot variants in Chinese patients with pheochromocytomas and paragangliomas. The Journal of clinical endocrinology and metabolism 2022 11 . Li Minghao, He Yazhi, Pang Yingxian, Zhang Jing, Feng Yu, He Yao, Xu Xiaowen, Wei Yongbao, Zhong Dewen, Deng Wanglong, Wang Long, Yan Bin, Jiang Yazhuo, Xu Ning, Cai Hai, Wen Yanlin, Ning Jinzhuo, Liu Yujun, Gao Xin, Shan Zhongyan, Liu Longfei, Teng Xiaochun, Richter Susan, Jiang Jingji |
Pseudohypoxic pheochromocytomas and paragangliomas dominate in children. Pediatric blood & cancer 2021 3 68 (7): e28981. Redlich Antje, Pamporaki Christina, Lessel Lienhard, Frühwald Michael C, Vorwerk Peter, Kuhlen Michae |
Functional significance of germline EPAS1 variants. Endocrine-related cancer 2020 12 28 (2): 97-109. Dwight Trisha, Kim Edward, Bastard Karine, Benn Diana E, Eisenhofer Graeme, Richter Susan, Mannelli Massimo, Rapizzi Elena, Prejbisz Aleksander, P?czkowska Mariola, Pacak Karel, Clifton-Bligh Roderi |
Genotype-phenotype correlations in pheochromocytoma and paraganglioma: a systematic review and individual patient meta-analysis. Endocrine-related cancer 2019 Mar . Crona Joakim, Lamarca Angela, Ghosal Suman, Welin Staffan, Skogseid Britt, Pacak Kar |
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. The Journal of clinical endocrinology and metabolism 2014 Jul 99 (7): E1352-60. Welander Jenny, Andreasson Adam, Juhlin C Christofer, Wiseman Roger W, Bäckdahl Martin, Höög Anders, Larsson Catharina, Gimm Oliver, Söderkvist Pet |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: