Management of endocrine disease: Cushing's syndrome due to ectopic ACTH secretion: an expert operational opinion
…, O Viera-Pinto, O Chabre… - European journal of …, 2020 - academic.oup.com
Ectopic ACTH syndrome (EAS) is rare but is frequently a severe condition because of the
intensity of the hypercortisolism that may be dissociated from the tumoral condition. EAS …
intensity of the hypercortisolism that may be dissociated from the tumoral condition. EAS …
[HTML][HTML] MicroRNA therapeutics in cancer: current advances and challenges
… this hurdle, several strategies have been devised, including chemical modifications such
as phosphodiester and phosphorothioate internucleotide linkages, addition of a 2′-O-methyl …
as phosphodiester and phosphorothioate internucleotide linkages, addition of a 2′-O-methyl …
Exploration and management of adrenal incidentalomas.: French Society of Endocrinology Consensus
…, S Bardet, J Bertherat, B Dupas, O Chabre… - Annales d' …, 2008 - Elsevier
The French Society of Endocrinology convened a multidisciplinary panel of endocrinologists,
radiologists, nuclear physicians and surgeons to address the appropriate evaluation and …
radiologists, nuclear physicians and surgeons to address the appropriate evaluation and …
[PDF][PDF] Genetic testing in pheochromocytoma or functional paraganglioma
…, B Bressac-de Paillerets, O Chabre… - Journal of Clinical …, 2005 - Citeseer
… Laurence Amar, Jérôme Bertherat, Eric Baudin, Christiane Ajzenberg, Brigitte Bressac-de
Paillerets, Olivier Chabre, Bernard Chamontin, Brigitte Delemer, Sophie Giraud, Arnaud …
Paillerets, Olivier Chabre, Bernard Chamontin, Brigitte Delemer, Sophie Giraud, Arnaud …
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
…, C Soukaseum, C Mandet, F Broux, O Chabre… - Nature …, 2012 - nature.com
Familial hyperkalemic hypertension (FHHt) is a Mendelian form of arterial hypertension that
is partially explained by mutations in WNK1 and WNK4 that lead to increased activity of the …
is partially explained by mutations in WNK1 and WNK4 that lead to increased activity of the …
Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families
…, B Estour, P Lecomte, B Gatta, O Chabre… - The Journal of …, 2007 - academic.oup.com
Context: An association between germline aryl hydrocarbon receptor-interacting protein (AIP)
gene mutations and pituitary adenomas was recently shown. Objective: The objective of …
gene mutations and pituitary adenomas was recently shown. Objective: The objective of …
The European Registry on Cushing's syndrome: 2-year experience. Baseline demographic and clinical characteristics
…, P Chanson, JAH Wass, O Chabre… - European journal of …, 2011 - academic.oup.com
Objective The European Registry on Cushing's syndrome (ERCUSYN) is designed to
collect prospective and follow-up data at EU level on Cushing's syndrome (CS). Design and …
collect prospective and follow-up data at EU level on Cushing's syndrome (CS). Design and …
Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas
…, L Amar, S Azriel, I Bourdeau, O Chabre… - Human molecular …, 2014 - academic.oup.com
Malignant pheochromocytoma (PCC) and paraganglioma (PGL) are mostly caused by
germline mutations of SDHB, encoding a subunit of succinate dehydrogenase. Using whole-…
germline mutations of SDHB, encoding a subunit of succinate dehydrogenase. Using whole-…
Ketoconazole in Cushing's disease: is it worth a try?
Background: The use of ketoconazole has been recently questioned after warnings from the
European Medicine Agencies and the Food and Drug Administration due to potential …
European Medicine Agencies and the Food and Drug Administration due to potential …
Gene expression profiling of human adrenocortical tumors using complementary deoxyribonucleic acid microarrays identifies several candidate genes as markers of …
…, F Berger, C Gicquel, O Chabre… - The Journal of …, 2005 - academic.oup.com
The aim of this study was to identify predictor sets of genes whose over- or underexpression
in human sporadic adrenocortical tumors would help to identify malignant vs. benign tumors …
in human sporadic adrenocortical tumors would help to identify malignant vs. benign tumors …