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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 25, 2015
Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and ParagangliomasRodrigo A Toledo, Yuejuan Qin, Zi-Ming Cheng, et al.
Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
Endocrine-Related Cancer|October 31, 2013
Long-term prognosis of patients with pediatric pheochromocytomaBirke Bausch, Ulrich Wellner, Dirk Bausch, et al.
Head & Neck|April 14, 2015
Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor RegistryBirke Bausch, Ulrich Wellner, Mathieu Peyre, et al.
Plos Genetics|August 17, 2005
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomasPatricia L M Dahia, Ken N Ross, Matthew E Wright, et al.
JAMA|December 16, 2010
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomasLi Yao, Francesca Schiavi, Alberto Cascon, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2007
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1Birke Bausch, Wiktor Borozdin, Victor F Mautner, et al.
The Journal of Clinical Endocrinology and Metabolism|October 14, 2020
Genotype-Phenotype Features of Germline Variants of the TMEM127 Pheochromocytoma Susceptibility Gene: A 10-Year UpdateGustavo Armaiz-Pena, Shahida K Flores, Zi-Ming Cheng, et al.
Human Mutation|October 28, 2010
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10Karin Frank-Raue, Lisa A Rybicki, Zoran Erlic, et al.
The Lancet. Oncology|April 22, 2014
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based studyFrederic Castinetti, Xiao-Ping Qi, Martin K Walz, et al.
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