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1. Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement

2. Sunitinib for metastatic progressive phaeochromocytomas and paragangliomas: results from FIRSTMAPPP, an academic, multicentre, international, randomised, placebo-controlled, double-blind, phase 2 trial

3. MAML3-fusions modulate vascular and immune tumour microenvironment and confer high metastatic risk in pheochromocytoma and paraganglioma

4. Recommandations du réseau national ENDOCAN-COMETE pour la prise en charge des phéochromocytomes et paragangliomes métastatiques

6. 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

7. Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants

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

11. Association of adrenal steroids with metabolomic profiles in patients with primary and endocrine hypertension

12. EPAS1‐mutated paragangliomas associated with haemoglobin disorders

13. International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers

15. Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

16. Update of the UMD-VHL database: classification of 164 challenging variants based on genotype-phenotype correlation among 605 entries.

19. Update of the UMD-VHL database: classification of 164 challenging variants based on genotype–phenotype correlation among 605 entries

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

24. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.

25. Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

27. The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

28. Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images

29. Molecular Characterization and Clinical Relevance of Metabolic Expression Subtypes in Human Cancers

30. Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

31. Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

32. Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types

33. Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas

34. Systematic Analysis of Splice-Site-Creating Mutations in Cancer

35. Driver Fusions and Their Implications in the Development and Treatment of Human Cancers

36. Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

37. Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types

38. Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations

39. LHCG Receptor in pheochromocytoma

40. Paraganglioma, Malignant

41. Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients

42. International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents

44. Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension

45. A call to action and a lifecourse strategy to address the global burden of raised blood pressure on current and future generations: the Lancet Commission on hypertension

46. supplemental legend from DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

47. Data from Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and Paraganglioma

48. Supplementary data from In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma

49. Data from Loss of SDHB Promotes Dysregulated Iron Homeostasis, Oxidative Stress, and Sensitivity to Ascorbate

50. Supplemental Figure 1 from DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

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