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2. Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions

3. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence

4. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

5. Efficacy and Safety of Eculizumab in Pediatric Patients Affected by Shiga Toxin–Related Hemolytic and Uremic Syndrome: A Randomized, Placebo-Controlled Trial

6. Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathy

8. What is the impact of blood pressure on neurological symptoms and the risk of ESKD in primary and secondary thrombotic microangiopathies based on clinical presentation: a retrospective study

9. Social Deprivation Is Associated With Lower Access to Pre-emptive Kidney Transplantation and More Urgent-Start Dialysis in the Pediatric Population

10. Renal Prognosis in Children With Tubulointerstitial Nephritis and Uveitis Syndrome

11. Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease

12. Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

14. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants is Not Associated with Post-Transplant Recurrence

15. School level of children carrying a HNF1B variant or a deletion

16. Acute tubulointerstitial nephritis with or without uveitis: a novel form of post-acute COVID-19 syndrome in children

17. Mortality risk disparities in children receiving chronic renal replacement therapy for the treatment of end-stage renal disease across Europe: an ESPN-ERA/EDTA registry analysis

18. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.

19. Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

20. Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

21. Infection in Patients with Suspected Thrombotic Microangiopathy Based on Clinical Presentation

23. Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease

24. The ANTENATAL multicentre study to predict postnatal renal outcome in fetuses with posterior urethral valves: objectives and design

25. Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

27. Spectrum of mutations in the renin–angiotensin system genes in autosomal recessive renal tubular dysgenesis

28. Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial

32. Blockade of the kallikrein-kinin system reduces endothelial complement activation in vascular inflammation

36. School level of children carrying a HNF1B variant or a deletion

37. Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment

38. Etiology and Outcomes of Thrombotic Microangiopathies

39. Elaboration of a semi-automated algorithm for brain arteriovenous malformation segmentation: initial results

40. Mortality risk disparities in children receiving chronic renal replacement therapy for the treatment of end-stage renal disease across Europe:an ESPN-ERA/EDTA registry analysis

41. Population pharmacokinetics and pharmacogenetics of mycophenolic acid following administration of mycophenolate mofetil in de novo pediatric renal-transplant patients

42. SP695EXPLAINING THE VARIATION IN COUNTRY MORTALITY RATES FOR PAEDIATRIC END-STAGE RENAL DISEASE ACROSS EUROPE - AN ESPN-ERA/EDTA REGISTRY ANALYSIS

43. Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

44. Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.

45. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome

46. Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis

47. Acute Neurological Involvement in Diarrhea-Associated Hemolytic Uremic Syndrome

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