345 results on '"Bertherat, Jerome"'
Search Results
2. Differentiation between adrenocortical carcinoma and lipid-poor adrenal adenoma using a multiparametric MRI-based diagnostic algorithm
3. Endocrine disrupting chemicals are a threat to hormone health: a commentary on behalf of the ESE
4. Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) for the diagnosis of Cushing's syndrome: Genetics of Cushing's syndrome
5. Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma
6. Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma
7. Sunitinib for metastatic progressive phaeochromocytomas and paragangliomas: results from FIRSTMAPPP, an academic, multicentre, international, randomised, placebo-controlled, double-blind, phase 2 trial
8. Diagnostic performance of an automated immunoassay for salivary cortisol
9. The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network
10. Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)
11. Adjuvant mitotane versus surveillance in low-grade, localised adrenocortical carcinoma (ADIUVO): an international, multicentre, open-label, randomised, phase 3 trial and observational study
12. Recommandations du réseau national ENDOCAN-COMETE pour la prise en charge des phéochromocytomes et paragangliomes métastatiques
13. Recommandations conjointes du réseau National ENDOCAN-COMETE, de l’Association francophone de chirurgie endocrinienne et de la Société française d’urologie pour la prise en charge du carcinome corticosurrénalien
14. Perioperative outcomes of pheochromocytoma/paraganglioma surgery preceded by Takotsubo-like cardiomyopathy
15. Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome
16. Molecular Alterations of the cAMP Signaling Leading to Endocrine Tumors : Focus on the Carney Complex and McCune-Albright Syndrome
17. Consensus on diagnosis and management of Cushing's disease: a guideline update
18. Surgical management of insulinoma over three decades
19. Results of systematic KDM1A genotyping in a large series of Primary Bilateral Macronodular Adrenal Hyperplasia (PBMAH) patients and analysis of the genotype/phenotype correlation
20. PAM expression in pituitary neuroendocrine tumors (PitNETs)
21. Intra-tissular profile of adrenal steroids reveals variable levels associated with adrenocortical tumors (ACT) differentiation and suggests alterations in steroids export
22. Decrease in anticortisolic drmg osilodrostat plasma exposure in patients treated with mitotane for adrenocortical carcinoma
23. Long-term safety and efficacy of subcutaneous pasireotide in patients with cushing's disease: results from a non-interventional study
24. Diseases Predisposing to Adrenocortical Malignancy (Li–Fraumeni Syndrome, Beckwith–Wiedemann Syndrome, and Carney Complex)
25. Adrenal Tumours: Adrenocortical Functioning Adenomas, Pheochromocytomas, Incidentalomas, and Adrenocortical Cancer
26. Urine steroid metabolomics for the differential diagnosis of adrenal incidentalomas in the EURINE-ACT study: a prospective test validation study
27. Adrenalectomy during pregnancy: A 15-year experience at a tertiary referral center
28. The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia
29. Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation.
30. Pre- and intraoperative diagnostic requirements, benefits and risks of minimally invasive and robotic surgery for neuroendocrine tumors of the pancreas
31. THU504 Is Carney Complex A Predisposing Syndrome For Breast Cancer? Prospective Study Of 50 Women
32. OR08-01 Expression of Gonadal Differentiation Markers in Bilateral Macronodular Adrenocortical Disease
33. Decrease in anticortisolic drug osilodrostat plasma exposure in patients treated with mitotane for an adrenocortical carcinoma
34. Transcriptome in paraffin samples for the diagnosis and prognosis of pituitary neuroendocrine tumors (PITNETS)
35. Whole blood transcriptomic signature of Cushing's syndrome
36. Proposition of an histopathological classification of bilateral macronodular adrenal disease (BMAD) and its correlation with ARMC5 and KDM1A mutations
37. Constitutional duplication of PRKACA gene is a cause of isolated primary pigmented nodular adrenocortical disease (PPNAD): Results of its systematic search in bilateral nodular adrenal disease
38. Carney Complex
39. Adrenocortical Cancer
40. Genetics of Adrenocortical Cancers
41. Endocrine side-effects of new anticancer therapies: Overall monitoring and conclusions
42. SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook
43. The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)
44. Clinicopathological description of 43 oncocytic adrenocortical tumors: importance of Ki-67 in histoprognostic evaluation
45. Group 1. Epidemiology of primary and secondary adrenal insufficiency: Prevalence and incidence, acute adrenal insufficiency, long-term morbidity and mortality
46. Evidence of Persistent Mild Hypercortisolism in Patients Medically Treated for Cushing Disease: the Haircush Study
47. Increased frequency of breast cancer in young Carney Complex patients suggests a role for inactivation of the tumor suppressor gene PRKAR1A
48. Prolonged Adrenocortical Blockade Following Interruption of Osilodrostat in ACTH-dependent Cushing's syndrome
49. Study of somatic molecular heterogeneity in bilateral macronodular adrenocortical disease (BMAD) by NGS panel in a cohort of 26 patients
50. Persistence of mild hypercortisolism in patients with Cushing's disease treated with cortisol-lowering drugs : the Haircush study
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