284 results on '"Libé, Rossella"'
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2. Adjuvant mitotane versus surveillance in low-grade, localised adrenocortical carcinoma (ADIUVO): an international, multicentre, open-label, randomised, phase 3 trial and observational study
3. Recommandations du réseau national ENDOCAN-COMETE pour la prise en charge des phéochromocytomes et paragangliomes métastatiques
4. Outcome of adrenocortical carcinoma patients included in early phase clinical trials: Results from the French network ENDOCAN-COMETE
5. 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
6. Adrenocortical carcinoma: Diagnosis, prognostic classification and treatment of localized and advanced disease
7. Positive Correlation Between 18F-FDG Uptake and Tumor-Proliferating Antigen Ki-67 Expression in Adrenocortical Carcinomas
8. Medical management of adrenocortical carcinoma: Current recommendations, new therapeutic options and future perspectives
9. Whole blood transcriptomic signature of Cushing's syndrome.
10. Urine steroid metabolomics for the differential diagnosis of adrenal incidentalomas in the EURINE-ACT study: a prospective test validation study
11. Artistic movements as pitfalls in iconodiagnosis
12. Adrenocortical Cancer
13. Clinicopathological description of 43 oncocytic adrenocortical tumors: importance of Ki-67 in histoprognostic evaluation
14. Combined 68Ga-DOTATOC and 18F-FDG PET Predicts a Double Component With Different Grade of a Pancreatic Neuroendocrine Tumor in a Patient With Multiple Endocrine Neoplasia Type 1
15. Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.
16. Artistic movements as pitfalls in iconodiagnosis
17. A pheochromocytoma wrapped in an IgG4-related disease
18. Correction to: A pheochromocytoma wrapped in an IgG4-related disease
19. Laparoscopic or Open Adrenalectomy for Stage I–II Adrenocortical Carcinoma: A Retrospective Study
20. Supplementary Tables S1-S2 from β-Catenin Activation Is Associated with Specific Clinical and Pathologic Characteristics and a Poor Outcome in Adrenocortical Carcinoma
21. Supplementary Table 2 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
22. Supplementary Table 3 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
23. Data from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
24. Supplementary Table 1 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
25. Corticosurrénalome et grossesse
26. Thyroid swellings in Renaissance illuminations
27. OR12-3 Identification of Predictive Criteria for the Primary Bilateral Macronodular Adrenal Hyperplasia Gene ARMC5: A European Series of 352 Unselected Patients.
28. OR04-3 Genetic Alterations of ARMC5 and KDM1A Are Associated With Different Expression Profiles of Illegitimate Receptors in Primary Bilateral Macronodular Adrenal Hyperplasia
29. Rasch analysis for assessing unidimensionality and identifying measurement biases of malignancy scores in oncology. The example of the Weiss histopathological system for the diagnosis of adrenocortical cancer
30. 18F-FDG PET reveals an adrenocortical carcinoma in a bilateral adrenal multinodular disease
31. Assessment of VAV2 Expression Refines Prognostic Prediction in Adrenocortical Carcinoma
32. Adrenocortical Cancer
33. Positive Correlation Between 18 F-FDG Uptake and Tumor-Proliferating Antigen Ki-67 Expression in Adrenocortical Carcinomas.
34. Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients
35. List of Contributors
36. Genetics of Adrenocortical Tumors (ACT) and Hypersecretory Syndromes
37. KDM1A inactivation causes hereditary food-dependent Cushing syndrome
38. Adrenal Mass Characterization in the Era of Quantitative Imaging: State of the Art
39. Primary Aldosteronism and ARMC5 Variants
40. ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences
41. Rationale for Anti-angiogenic Therapy in Pheochromocytoma and Paraganglioma
42. Le corticosurrénalome : progrès dans la physiopathologie et la prise en charge d’un cancer rare
43. Macronodular Adrenal Hyperplasia due to Mutations in an Armadillo Repeat Containing 5 (ARMC5) Gene: A Clinical and Genetic Investigation
44. A Feminizing Adrenocortical Carcinoma in the Context of a Late Onset 21-Hydroxylase Deficiency
45. Preoperative Detection of Liver Involvement by Right-Sided Adrenocortical Carcinoma Using CT and MRI
46. LSD1/KDM1A Inactivation Causes Hereditary Food-Dependent Cushing’s Syndrome
47. Intraadrenal Corticotropin in Bilateral Macronodular Adrenal Hyperplasia
48. ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushingʼs Syndrome
49. One-Year Progression-Free Survival of Therapy-Naive Patients With Malignant Pheochromocytoma and Paraganglioma
50. Imaging Work-Up for Screening of Paraganglioma and Pheochromocytoma in SDHx Mutation Carriers: A Multicenter Prospective Study from the PGL.EVA Investigators
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