All Stories

  1. Diagnosing a genetic disease in a donor-conceived child: case report and discussion of the ethical, legal, and practical issues
  2. On the Importance of Considering Glycosylation When Evaluating Biologic Therapies
  3. A Guide for Adult Nephrologists and Hematologists to Managing Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy in Teens Transitioning to Young Adults
  4. Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis
  5. Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice
  6. Inherited Kidney Complement Diseases
  7. Novel Fanconi renotubular syndromes provide insights in proximal tubule pathophysiology
  8. The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort
  9. Canadian Association of Paediatric Nephrologists COVID-19 Rapid Response: Guidelines for Management of Acute Kidney Injury in Children
  10. Canadian Association of Paediatric Nephrologists COVID-19 Rapid Response: Home and In-Center Dialysis Guidance
  11. 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
  12. Helping nephrologists find answers: hyperinsulinism and tubular dysfunction: Answers
  13. Helping nephrologists find answers: hyperinsulinism and tubular dysfunction: Questions
  14. SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes
  15. Phosphatidylinositol Cycle Disruption is Central to Atypical Hemolytic-Uremic Syndrome Caused by Diacylglycerol Kinase Epsilon Deficiency
  16. Driving Medical Innovation Through Interdisciplinarity: Unique Opportunities and Challenges
  17. Opportunities and Challenges for Genetic Studies of End-Stage Renal Disease in Canada
  18. A Perspective on Inherited Kidney Disease
  19. Management of Severe Hyponatremia With a Custom Continuous Renal Replacement Therapy in an Infant With Newly Diagnosed Chronic Kidney Disease
  20. Neonatal stroke and haematuria: Answers
  21. Neonatal stroke and haematuria: Questions
  22. The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinaseε
  23. A variant in a cis -regulatory element enhances claudin-14 expression and is associated with pediatric-onset hypercalciuria and kidney stones
  24. Diacylglycerol kinase epsilon suppresses expression of p53 and glycerol kinase in mouse embryo fibroblasts
  25. Diacylglycerol Kinase-ε: Properties and Biological Roles
  26. When Langerhans' and Cajal's worlds collide, diabetics win
  27. A new DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical HUS
  28. Autism heritability: A new twist on familial genetics?
  29. RSV Bronchiolitis: Tale of an Overzealous Helper?
  30. Superheroes and Villains of the Heart
  31. Human Cells: Finally Open for Cancer Business
  32. For IBD, Bugs and Genes Are the Name of the Game
  33. WANTED: Natural-Born Sickler
  34. PGE2--The Immune System Tamer
  35. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
  36. 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
  37. Treatment of paediatric vancomycin intoxication: a case report and review of the literature
  38. Whole or parts—the fate of hemoperitoneum
  39. Rapid Tumor Cell Swelling and Bursting: Beware of Collateral Damage
  40. Index of Suspicion
  41. A novel disease-causing mutation in AVPR2: Q96H
  42. Subgroup analysis: at best suggestive (rather than conclusive)
  43. Treatment for otitis media
  44. Acidosis in a patient with cholera: a need to redefine concepts
  45. Twitching and quivering of the tentacles during snail olfactory orientation