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8. Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome

9. From Nelson's Syndrome to Corticotroph Tumor Progression Speed: An Update.

10. Positive Correlation Between 18F-FDG Uptake and Tumor-Proliferating Antigen Ki-67 Expression in Adrenocortical Carcinomas

11. TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome

12. Whole blood methylome-derived features to discriminate endocrine hypertension

13. Prognostic Impact of Hypothalamic Perforation in Adult Patients With Craniopharyngioma: A Cohort Study.

14. Whole blood transcriptomic signature of Cushing's syndrome.

15. A computed tomography-based radiomic score to predict survival in patients with adrenocortical carcinoma

16. Carney complex predisposes to breast cancer: prospective study of 50 women

17. Artificial Intelligence in Endocrinology: On Track Toward Great Opportunities.

18. THU504 Is Carney Complex A Predisposing Syndrome For Breast Cancer? Prospective Study Of 50 Women

19. FRI135 Differential Expression Of Circulating MicroRNAs In Primary Aldosteronism: Potential Biomarkers For Improved Diagnosis

20. Embryonic stem cell factor FOXD3 (Genesis) defects in gastrointestinal stromal tumors

21. The super-enhancer landscape reflects molecular subgroups of adrenocortical carcinoma

23. Supplementary Table 2 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers

24. Supplementary Table 3 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers

26. Supplementary Table 1 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers

27. C-peptide level concomitant with hypoglycemia gives better performances than insulin for the diagnosis of endogenous hyperinsulinism: a single-center study of 159 fasting trials

28. Corticotroph tumor progression speed after adrenalectomy

29. OR12-3 Identification of Predictive Criteria for the Primary Bilateral Macronodular Adrenal Hyperplasia Gene ARMC5: A European Series of 352 Unselected Patients.

30. OR04-3 Genetic Alterations of ARMC5 and KDM1A Are Associated With Different Expression Profiles of Illegitimate Receptors in Primary Bilateral Macronodular Adrenal Hyperplasia

31. Machine learning for classification of hypertension subtypes using multi-omics: A multi-centre, retrospective, data-driven study

33. Outcome of giant pituitary tumors requiring surgery

34. Predicting Hypertension Subtypes with Machine Learning Using Targeted Metabolites and Their Ratios

35. Decreased steroidogenic enzyme activity in benign adrenocortical tumors is more pronounced in bilateral lesions as determined by steroid profiling in LC-MS/MS during ACTH stimulation test

36. Differences in the spectrum of steroidogenic enzyme inhibition between Osilodrostat and Metyrapone in ACTH-dependent Cushing syndrome patients

37. Identification of glucocorticoid-related molecular signature by whole blood methylome analysis

38. Positive Correlation Between 18 F-FDG Uptake and Tumor-Proliferating Antigen Ki-67 Expression in Adrenocortical Carcinomas.

39. Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients

40. Additional file 1 of Whole blood methylome-derived features to discriminate endocrine hypertension

41. Additional file 1 of TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome

42. Positive Correlation Between [18F]-fluorodeoxyglucose (FDG) Uptake and Tumor-proliferating Antigen Ki-67 Expression in Adrenocortical Carcinomas

43. Identification of glucocorticoid-related molecular signature by whole blood methylome analysis

44. KDM1A inactivation causes hereditary food-dependent Cushing syndrome

45. Adrenal Mass Characterization in the Era of Quantitative Imaging: State of the Art

46. Pituitary surgery as alternative to dopamine agonists treatment for microprolactinomas: a cohort study

47. Contributors

48. KDM1Ainactivation causes hereditary food-dependent Cushing syndrome

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