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Scientific Reports|July 1, 2025
PGL-EXPO feasibility study of exposure to SDHi fungicides and risk of hereditary SDHx paraganglioma or pheochromocytomaAstrid Coste, Alexandre Buffet, Margaux Duboeuf, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 31, 2010
Endolymphatic sac tumors in von Hippel-Lindau disease: report of three casesCorneliu-Mircea Codreanu, Michèle Duet, Charlotte Hautefort, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|September 22, 2009
A role for succinate dehydrogenase genes in low chemoresponsiveness to hypoxia?Jean-Paul Richalet, Anne-Paule Gimenez-Roqueplo, Séverine Peyrard, et al.
Cancers|August 30, 2020
Usefulness of FDG-PET/CT-Based Radiomics for the Characterization and Genetic Orientation of Pheochromocytomas Before SurgeryCatherine Ansquer, Delphine Drui, Eric Mirallié, et al.
Cancer Research|February 13, 2018
Germline Mutations in the Mitochondrial 2-Oxoglutarate/Malate Carrier SLC25A11 Gene Confer a Predisposition to Metastatic ParagangliomasAlexandre Buffet, Aurélie Morin, Luis-Jaime Castro-Vega, et al.
International Journal of Cancer|April 23, 2014
SDHB mutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paragangliomaJulien Hadoux, Judith Favier, Jean-Yves Scoazec, et al.
The Journal of Clinical Endocrinology and Metabolism|November 17, 2009
Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomasJosé Gaal, Nelly Burnichon, Esther Korpershoek, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2007
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomasLaurence Amar, Eric Baudin, Nelly Burnichon, et al.
Clinical Endocrinology|October 28, 2016
Pheochromocytomas are diagnosed incidentally and at older age in neurofibromatosis type 1Jessica Moramarco, Nada El Ghorayeb, Nadine Dumas, et al.
Journal of Medical Genetics|August 28, 2021
International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytomaLaurene Ben Aim, Eamonn R Maher, Alberto Cascon, et al.
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