All Stories

  1. Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol
  2. IPNA clinical practice recommendations on care of pediatric patients with pre-existing kidney disease during seasonal outbreak of COVID-19
  3. Urinary chloride excretion in critical illness and acute kidney injury: a paediatric hypothesis-generating cohort study post cardiopulmonary bypass surgery
  4. Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years
  5. Rare SH2B3 coding variants in lupus patients impair B cell tolerance and predispose to autoimmunity
  6. Relationship between cortical and medullary thickness and glomerular filtration rate among living kidney donors
  7. Effect of Saline vs Gluconate/Acetate–Buffered Solution vs Lactate-Buffered Solution on Serum Chloride Among Children in the Pediatric Intensive Care Unit
  8. Diagnostic and therapeutic management of vesico‐ureteral reflux in pediatric kidney transplantation—Results of an online survey on behalf of the European Society for Paediatric Nephrology
  9. The Evolving Role of Diagnostic Genomics in Kidney Transplantation
  10. Serum and urinary biomarkers to predict acute kidney injury in premature infants: a systematic review and meta-analysis of diagnostic accuracy
  11. WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review
  12. Improve in-depth immunological risk assessment to optimize genetic-compatibility and clinical outcomes in child and adolescent recipients of parental donor kidney transplants: protocol for the INCEPTION study
  13. Urinary Chloride Excretion Postcardiopulmonary Bypass in Pediatric Patients—A Pilot Study
  14. Effectiveness of growth hormone on growth and final height in paediatric chronic kidney disease
  15. 0.9% Sodium chloride solution versus Plasma-Lyte 148 versus compound sodium lacTate solution in children admitted to PICU—a randomized controlled trial (SPLYT-P): study protocol for an intravenous fluid therapy trial
  16. Renal tumors in tuberous sclerosis complex
  17. A Rare and Unusual Cause of Unilateral Ureteric Obstruction in a Child
  18. Protocol and establishment of a Queensland renal biopsy registry in Australia
  19. Acute Hemorrhagic Leukoencephalopathy: Pathological Features and Cerebrospinal Fluid Cytokine Profiles
  20. The impact of prematurity on postnatal growth of different renal compartments
  21. Treatment and long-term outcome in primary distal renal tubular acidosis
  22. Renal genetics in Australia: Kidney medicine in the genomic age
  23. Antenatally Diagnosed ADPKD
  24. The impact of donor/recipient age difference and HLA mismatch on graft outcome in pediatric kidney transplantation
  25. Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms
  26. Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome
  27. Long-Term Outcome of Kidney Transplantation in Recipients with Focal Segmental Glomerulosclerosis
  28. A protocol for the identification and validation of novel genetic causes of kidney disease
  29. A retrospective review of telehealth services for children referred to a paediatric nephrologist
  30. KHA-CARI guideline: Diagnosis and treatment of urinary tract infection in children
  31. Reninoma: An Uncommon Cause of Renin-Mediated Hypertension
  32. Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
  33. Henoch-Schönlein purpura in children
  34. Urinary tract obstruction in the mouse: the kinetics of distal nephron injury
  35. Progressive multifocal leukoencephalopathy with gastrointestinal disease in a pediatric kidney transplant recipient
  36. Congenital urinary tract obstruction: defining markers of developmental kidney injury
  37. Urinary Biomarkers in Obstructive Nephropathy
  38. Hypothesis: SLC12A3 Polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistance
  39. Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
  40. Phenotypic Transition of the Collecting Duct Epithelium in Congenital Urinary Tract Obstruction
  41. Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy
  42. Selected Primary Care Issues and Comorbidities in Children Who Are on Maintenance Dialysis: A Review for the Pediatric Nephrologist
  43. CANDIDURIA IN CRITICALLY ILL CHILDREN