128 results on '"Schaefer, Franz"'
Search Results
2. Clinical practice recommendations for kidney involvement in tuberous sclerosis complex: a consensus statement by the ERKNet Working Group for Autosomal Dominant Structural Kidney Disorders and the ERA Genes & Kidney Working Group
3. Worldwide disparities in access to treatment and investigations for nephropathic cystinosis: a 2023 perspective
4. Perception and knowledge of pediatric nephrologists on evidence-based guideline development methodology
5. Urine soluble TLR4 levels may contribute to predict urinary tract infection in children: the UTILISE Study
6. Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease
7. Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries
8. Versorgernetzwerke für Menschen mit Seltenen Erkrankungen: Daten und Expertise bündeln
9. Clinical characteristics and outcomes of a patient population with atypical hemolytic uremic syndrome and malignant hypertension: analysis from the Global aHUS registry
10. Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study
11. Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group
12. Dialysis disequilibrium syndrome (DDS) in pediatric patients on dialysis: systematic review and clinical practice recommendations
13. Impact of COVID-19 pandemic on use of rituximab among children with difficult nephrotic syndrome
14. Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease—are patient-centered outcomes our blind spot?
15. Current management of transition of young people affected by rare renal conditions in the ERKNet
16. The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results
17. Publisher Correction: Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group
18. European Reference Networks: challenges and opportunities
19. Hemodiafiltration maintains a sustained improvement in blood pressure compared to conventional hemodialysis in children—the HDF, heart and height (3H) study
20. U-IMD: the first Unified European registry for inherited metabolic diseases
21. Differential assessment of fluid compartments by bioimpedance in pediatric patients with kidney diseases
22. Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group
23. Randomized clinical trial to compare efficacy and safety of repeated courses of rituximab to single-course rituximab followed by maintenance mycophenolate-mofetil in children with steroid dependent nephrotic syndrome
24. Renal developmental genes are differentially regulated after unilateral ureteral obstruction in neonatal and adult mice
25. Pediatric kidney transplantation in China: an analysis from the IPNA Global Kidney Replacement Therapy Registry
26. Pathophysiology and consequences of arterial stiffness in children with chronic kidney disease
27. Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working group
28. Targeting optimal PD management in children: what have we learned from the IPPN registry?
29. Cinacalcet studies in pediatric subjects with secondary hyperparathyroidism receiving dialysis
30. Consensus guidelines for management of hyperammonaemia in paediatric patients receiving continuous kidney replacement therapy
31. Implications of early diagnosis of autosomal dominant polycystic kidney disease: A post hoc analysis of the TEMPO 3:4 trial
32. Prenatal alcohol exposure affects renal function in overweight schoolchildren: birth cohort analysis
33. Indoxyl sulfate associates with cardiovascular phenotype in children with chronic kidney disease
34. Impaired Systolic and Diastolic Left Ventricular Function in Children with Chronic Kidney Disease - Results from the 4C Study
35. Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney disease
36. Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)
37. International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people
38. Tolvaptan use in children and adolescents with autosomal dominant polycystic kidney disease: rationale and design of a two-part, randomized, double-blind, placebo-controlled trial
39. Urinary proteome signature of Renal Cysts and Diabetes syndrome in children
40. Urinary acute kidney injury biomarkers in very low-birth-weight infants on indomethacin for patent ductus arteriosus
41. Pediatric intradialytic hypotension: recommendations from the Pediatric Continuous Renal Replacement Therapy (PCRRT) Workgroup
42. Hemodialysis vascular access and subsequent transplantation: a report from the ESPN/ERA-EDTA Registry
43. A randomized, double-blind, placebo-controlled study to assess the efficacy and safety of cinacalcet in pediatric patients with chronic kidney disease and secondary hyperparathyroidism receiving dialysis
44. Cardiovascular risk factors in children on dialysis: an update
45. Genetic associations of hemoglobin in children with chronic kidney disease in the PediGFR Consortium
46. Effect of haemodiafiltration vs conventional haemodialysis on growth and cardiovascular outcomes in children – the HDF, heart and height (3H) study
47. Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms?
48. Validating the use of bioimpedance spectroscopy for assessment of fluid status in children
49. pH-mediated upregulation of AQP1 gene expression through the Spi-B transcription factor
50. Renal replacement therapy for children throughout the world: the need for a global registry
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