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1. Effects of mitotane on testicular adrenal rest tumors in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a retrospective series of five patients

2. Congenital adrenal hyperplasia - current insights in pathophysiology, diagnostics and management

3. Phase 3 and extension study of modified-release hydrocortisone in the treatment of congenital adrenal hyperplasia

4. Impact of cancer chemotherapy before ovarian cortex cryopreservation on ovarian tissue transplantation

6. Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21‑hydroxylase deficiency in Europe

7. Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

8. Puberty and fertility in classic galactosemia

9. Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia

10. Transition of young adults with endocrine and metabolic diseases: the TRANSEND cohort

11. Idiopathic central precocious puberty in a Klinefelter patient: highlights on gonadotropin levels and pathophysiology

13. Next Generation Sequencing Should Be Proposed to Every Woman With 'Idiopathic' Primary Ovarian Insufficiency

14. Effect of congenital adrenal hyperplasia treated by glucocorticoids on plasma metabolome: a machine-learning-based analysis

15. Positive association between progestins and the evolution of multiple fibroadenomas in 72 women

16. MON-LB308 Studying the Care and Social Pathway of Young Adults With Endocrine and Metabolic Diseases During Transition: The 'Transend' Cohort

17. Increased long QT and torsade de pointes reporting on tamoxifen compared with aromatase inhibitors

18. Endocrine perturbations in POEMS syndrome: Misunderstood features of a rare paraneoplastic syndrome

19. MANAGEMENT OF ENDOCRINE DISEASE: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: update on the management of adult patients and prenatal treatment

20. Paul Kelly, PhD (1943–2018)

21. Premature ovarian insufficiency: step-by-step genetics bring new insights

22. GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome

23. Diabetes Mellitus, Extreme Insulin Resistance, and Hypothalamic-Pituitary Langerhans Cells Histiocytosis

24. European observational study of ketoconazole for endogenous cushing's syndrome in collaboration with European registry on cushing's syndrome ERCUSYN: PASS ketoconazole study design and rationale

25. Abnormal serotonin regulatory loop in adrenals of patients with Cushing's syndrome and 21-hydroxylase deficiency

26. MON-224 Congenital Hypogonadotropic Hypogonadism: Features and Genetics of 60 Females Patients

27. SAT-444 Pituitary Function and the Response to GH Replacement Therapy in Patients with Histiocytosis: Analysis of the Pfizer International Metabolic Database (KIMS)

28. Post-transplant outcome of ovarian tissue cryopreserved after chemotherapy in hematological malignancies

29. Gain-of-function Prolactin Receptor Variants Are Not Associated With Breast Cancer and Multiple Fibroadenoma Risk

30. Un programme d’éducation thérapeutique centré sur la transition des patients, avec endocrinopathie chronique, entre les services d’endocrinologie pédiatrique et adulte

31. Postprandial GLP-1 Secretion After Bariatric Surgery in Three Cases of Severe Obesity Related to Craniopharyngiomas

32. Fertility and Pregnancy in Patients With 21-Hydroxylase Deficiency

33. Endocrine manifestations in a cohort of 63 adulthood and childhood onset patients with Langerhans cell histiocytosis

34. Surgery Is Not Superior to Dilation for the Management of Vaginal Agenesis in Mayer-Rokitansky-Küster-Hauser Syndrome: A Multicenter Comparative Observational Study in 131 Patients

35. Endocrine Manifestations in a Monocentric Cohort of 64 Patients With Erdheim-Chester Disease

36. Prevalence of and Risk Factors for Anal Oncogenic Human Papillomavirus Infection Among HIV-Infected Women in France in the Combination Antiretroviral Therapy Era

37. Gynecologic follow up of 129 women on dialysis and after kidney transplantation: a retrospective cohort study

38. Challenges of the Transition from Pediatric Care to Care of Adults: 'Say Goodbye, Say Hello'

39. Early central blood pressure elevation in adult patients with 21-hydroxylase deficiency

40. Complex Association of Sex Hormones on Left Ventricular Systolic Function: Insight into Sexual Dimorphism

41. Managing Transition in Patients Treated with Growth Hormone

42. Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement

43. Prise en charge à l’âge adulte des hyperplasies congénitales des surrénales par déficit en 21-hydroxylase

44. Fertilité chez les femmes ayant un syndrome de Turner

45. Monocentric study of 112 consecutive patients with childhood onset GH deficiency around and after transition

46. Impact of transition on quality of life in patients with congenital adrenal hyperplasia diagnosed during childhood

47. French law: what about a reasoned reimbursement of serum vitamin D assays?

48. Poor Compliance to Hormone Therapy and Decreased Bone Mineral Density in Women with Premature Ovarian Insufficiency

49. MRI follow-up is unnecessary in patients with macroprolactinomas and long-term normal prolactin levels on dopamine agonist treatment

50. Hypoglycaemia revealing heterozygous insulin receptor mutations

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