71 results on '"Bertherat, Jerome"'
Search Results
2. 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
3. Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma
4. Sunitinib for metastatic progressive phaeochromocytomas and paragangliomas: results from FIRSTMAPPP, an academic, multicentre, international, randomised, placebo-controlled, double-blind, phase 2 trial
5. Diagnostic performance of an automated immunoassay for salivary cortisol
6. The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network
7. Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)
8. Adjuvant mitotane versus surveillance in low-grade, localised adrenocortical carcinoma (ADIUVO): an international, multicentre, open-label, randomised, phase 3 trial and observational study
9. Recommandations du réseau national ENDOCAN-COMETE pour la prise en charge des phéochromocytomes et paragangliomes métastatiques
10. 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
11. Perioperative outcomes of pheochromocytoma/paraganglioma surgery preceded by Takotsubo-like cardiomyopathy
12. Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome
13. Consensus on diagnosis and management of Cushing's disease: a guideline update
14. Surgical management of insulinoma over three decades
15. The molecular genetics of adrenal cushing.
16. Urine steroid metabolomics for the differential diagnosis of adrenal incidentalomas in the EURINE-ACT study: a prospective test validation study
17. Adrenalectomy during pregnancy: A 15-year experience at a tertiary referral center
18. Pre- and intraoperative diagnostic requirements, benefits and risks of minimally invasive and robotic surgery for neuroendocrine tumors of the pancreas
19. Endocrine side-effects of new anticancer therapies: Overall monitoring and conclusions
20. SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook
21. The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)
22. Clinicopathological description of 43 oncocytic adrenocortical tumors: importance of Ki-67 in histoprognostic evaluation
23. Group 1. Epidemiology of primary and secondary adrenal insufficiency: Prevalence and incidence, acute adrenal insufficiency, long-term morbidity and mortality
24. Corticosurrénalome et grossesse
25. Evidence of Persistent Mild Hypercortisolism in Patients Medically Treated for Cushing Disease: the Haircush Study.
26. SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T)
27. SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma
28. Clinical Biology of the Pituitary Adenoma.
29. Pathogenesis of benign adrenocortical tumors
30. The pathophysiology, diagnosis and prognosis of adrenocortical tumors revisited by transcriptome analyses
31. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
32. Cushing's disease
33. Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
34. The Weiss Score and Beyond—Histopathology for Adrenocortical Carcinoma
35. Heterogeneity of skin manifestations in patients with Carney complex
36. Le corticosurrénalome : progrès dans la physiopathologie et la prise en charge d’un cancer rare
37. SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samples
38. Pathologie thyroïdienne auto-immune
39. Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology: augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD
40. Frequent Phosphodiesterase 11A Gene (PDE11A) Defects in Patients with Carney Complex (CNC) Caused by PRKAR1A Mutations: PDE11A May Contribute to Adrenal and Testicular Tumors in CNC as a Modifier of the Phenotype
41. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study
42. High Diagnostic and Prognostic Value of Steroidogenic Factor-1 Expression in Adrenal Tumors
43. Pituitary surgery as alternative to dopamine agonists treatment for microprolactinomas: a cohort study.
44. Development of Novel Tools for the Diagnosis and Prognosis of Pheochromocytoma Using Peptide Marker Immunoassay and Gene Expression Profiling Approaches
45. ARMC5 variants in PRKAR1A-mutated patients modify cortisol levels and Cushing's syndrome.
46. The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia.
47. A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease.
48. Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad.
49. Differential Expression of Parathyroid Hormone-Related Protein in Adrenocortical Tumors: Autocrine/Paracrine Effects on the Growth and Signaling Pathways in H295R Cells.
50. Neural and Pituitary Mechanisms Involved in Growth Hormone Regulation.
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