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The Journal of Clinical Endocrinology and Metabolism|November 28, 2020
Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine PracticeClotilde Saie, Alexandre Buffet, Juliette Abeillon, et al.Cancer Letters|June 9, 2022
Dysfunction of calcium-regulated exocytosis at a single-cell level causes catecholamine hypersecretion in patients with pheochromocytomaSébastien Houy, Laura Streit, Inès Drissa, et al.Cancer Cell|May 28, 2013
SDH mutations establish a hypermethylator phenotype in paragangliomaEric Letouzé, Cosimo Martinelli, Céline Loriot, et al.Plos One|September 19, 2009
The Warburg effect is genetically determined in inherited pheochromocytomasJudith Favier, Jean-Jacques Brière, Nelly Burnichon, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 11, 2018
Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and ParagangliomaSylvie Job, Irena Draskovic, Nelly Burnichon, et al.Journal of Medical Genetics|March 17, 2019
Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paragangliomaLaurène Ben Aim, Pascal Pigny, Luis Jaime Castro-Vega, 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.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.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 23, 2015
In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in ParagangliomaCharlotte Lussey-Lepoutre, Alexandre Bellucci, Aurélie Morin, et al.Pageof 14