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2. Diagnosis and management of children and adult craniopharyngiomas: A French Endocrine Society/French Society for Paediatric Endocrinology & Diabetes Consensus Statement

3. Quality of life of chronically ill children and adolescents: a cross-sectional study

4. Dépistage et prise en charge du diabète de type 1 préclinique, stade 1–2. Prise de position d’experts français

5. Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP)

6. Diagnosis and management of congenital hypopituitarism in children

8. The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network

9. Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

10. Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)

11. Educational Needs and Type 1 Diabetes Mellitus: The Voices of Adolescents, Parents and Caregivers

13. Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia

14. Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine

15. New French height velocity growth charts: An innovative big‐data approach based on routine measurements.

17. Dépistage et prise en charge du diabète de type 1 préclinique, stade 1–2. Prise de position d’experts français

18. Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome)

20. Lessons from prospective longitudinal follow-up of a French APECED cohort

21. Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)

22. A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts

24. Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

25. Genetic testing in prolactinomas: a cohort study

26. The experience of diagnosis announcement in rare endocrine diseases: a survey of the French FIRENDO network

27. Family History is Underestimated in Children with Isolated Hypospadias: A French Multicenter Report of 88 Families

29. SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook

35. Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports

36. Motivational interviewing for the management of child and adolescent obesity: a systematic literature review.

38. The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing

41. Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia

42. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency

45. Genetic Landscape of a Large Cohort of Primary Ovarian Insufficiency: New Genes and Pathways and Implications for Personalized Medicine

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