All Stories

  1. Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney Disease
  2. Determining Causality in Gene Discovery
  3. When Nonspecific Symptoms Conceal Kidney Disease: A Case Report on Recognizing Juvenile Nephronophthisis in Pediatric Practice
  4. KRESCENT; 2005-2025 – 20 years! Editorial
  5. Diagnosing a genetic disease in a donor-conceived child: case report and discussion of the ethical, legal, and practical issues
  6. On the Importance of Considering Glycosylation When Evaluating Biologic Therapies
  7. A Guide for Adult Nephrologists and Hematologists to Managing Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy in Teens Transitioning to Young Adults
  8. Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis
  9. Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice
  10. Inherited Kidney Complement Diseases
  11. Novel Fanconi renotubular syndromes provide insights in proximal tubule pathophysiology
  12. The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort
  13. Canadian Association of Paediatric Nephrologists COVID-19 Rapid Response: Guidelines for Management of Acute Kidney Injury in Children
  14. Canadian Association of Paediatric Nephrologists COVID-19 Rapid Response: Home and In-Center Dialysis Guidance
  15. Management of Canadian Pediatric Patients With Glomerular Diseases During the COVID-19 Pandemic: Recommendations From the Canadian Association of Pediatric Nephrologists COVID-19 Rapid Response Team
  16. Helping nephrologists find answers: hyperinsulinism and tubular dysfunction: Answers
  17. Helping nephrologists find answers: hyperinsulinism and tubular dysfunction: Questions
  18. SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes
  19. Phosphatidylinositol Cycle Disruption is Central to Atypical Hemolytic-Uremic Syndrome Caused by Diacylglycerol Kinase Epsilon Deficiency
  20. Driving Medical Innovation Through Interdisciplinarity: Unique Opportunities and Challenges
  21. Opportunities and Challenges for Genetic Studies of End-Stage Renal Disease in Canada
  22. A Perspective on Inherited Kidney Disease
  23. Management of Severe Hyponatremia With a Custom Continuous Renal Replacement Therapy in an Infant With Newly Diagnosed Chronic Kidney Disease
  24. Neonatal stroke and haematuria: Answers
  25. Neonatal stroke and haematuria: Questions
  26. The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinaseε
  27. A variant in a cis -regulatory element enhances claudin-14 expression and is associated with pediatric-onset hypercalciuria and kidney stones
  28. Diacylglycerol kinase epsilon suppresses expression of p53 and glycerol kinase in mouse embryo fibroblasts
  29. Diacylglycerol Kinase-ε: Properties and Biological Roles
  30. When Langerhans' and Cajal's worlds collide, diabetics win
  31. A new DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical HUS
  32. Autism heritability: A new twist on familial genetics?
  33. RSV Bronchiolitis: Tale of an Overzealous Helper?
  34. Superheroes and Villains of the Heart
  35. Human Cells: Finally Open for Cancer Business
  36. For IBD, Bugs and Genes Are the Name of the Game
  37. WANTED: Natural-Born Sickler
  38. PGE2--The Immune System Tamer
  39. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
  40. Iron-containing micronutrient powder provided to children with moderate-to-severe malnutrition increases hemoglobin concentrations but not the risk of infectious morbidity: a randomized, double-blind, placebo-controlled, noninferiority safety trial
  41. Treatment of paediatric vancomycin intoxication: a case report and review of the literature
  42. Whole or parts—the fate of hemoperitoneum
  43. Rapid Tumor Cell Swelling and Bursting: Beware of Collateral Damage
  44. Index of Suspicion
  45. A novel disease-causing mutation in AVPR2: Q96H
  46. Subgroup analysis: at best suggestive (rather than conclusive)
  47. Treatment for otitis media
  48. Acidosis in a patient with cholera: a need to redefine concepts
  49. Twitching and quivering of the tentacles during snail olfactory orientation