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Oncotarget|October 14, 2015
Deciphering the molecular basis of invasiveness in Sdhb-deficient cellsCéline Loriot, Mélanie Domingues, Adeline Berger, et al.
Human Molecular Genetics|September 11, 2012
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytomaNelly Burnichon, Alexandre Buffet, Béatrice Parfait, et al.
Molecular and Cellular Endocrinology|July 1, 2015
From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytomaCharlotte Lepoutre-Lussey, Constance Thibault, Alexandre Buffet, et al.
European Journal of Endocrinology|October 13, 2004
A thyroid nodule revealing a paraganglioma in a patient with a new germline mutation in the succinate dehydrogenase B geneBaha Zantour, Brigitte Guilhaume, Frederique Tissier, et al.
Neuroendocrinology|January 26, 2017
The mTORC1 Complex Is Significantly Overactivated in SDHX-Mutated ParagangliomasLindsey Oudijk, Thomas Papathomas, Ronald de Krijger, et al.
Human Molecular Genetics|July 26, 2011
Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paragangliomaNelly Burnichon, Laure Vescovo, Laurence Amar, et al.
Orphanet Journal of Rare Diseases|June 9, 2007
Fibromuscular dysplasiaPierre-François Plouin, Jérôme Perdu, Agnès La Batide-Alanore, et al.
Clinical Endocrinology|October 23, 2002
Effects of slow-release octreotide on urinary metanephrine excretion and plasma chromogranin A and catecholamine levels in patients with malignant or recurrent phaeochromocytomaMaxime Lamarre-Cliche, Anne-Paule Gimenez-Roqueplo, Eliane Billaud, et al.
European Journal of Nuclear Medicine and Molecular Imaging|December 14, 2019
Succinate detection using in vivo 1H-MR spectroscopy identifies germline and somatic SDHx mutations in paragangliomasCharlotte Lussey-Lepoutre, Alexandre Bellucci, Nelly Burnichon, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2019
Transcriptome Analysis of lncRNAs in Pheochromocytomas and ParagangliomasSylvie Job, Adrien Georges, Nelly Burnichon, et al.
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