All Stories

  1. Pediatric kidney replacement therapies in low-to-middle income countries: a review and white paper
  2. Cyclophosphamide treatment with a comparison in both pediatric rheumatology and pediatric nephrology practices
  3. Comprehensive analysis of pediatric urolithiasis in a tertiary care center and insights into demographics, risk factors, and management outcomes
  4. Achievements, priorities and strategies in pediatric nephrology in Europe: need for unifying approaches or acceptance of differences?
  5. Publisher Correction: Rituximab-associated hypogammaglobulinemia in children with idiopathic nephrotic syndrome: results of an ESPN survey
  6. Plasmapheresis for the treatment of IgA vasculitis nephritis in children: A case series
  7. Diagnosis, management and treatment of the Alport syndrome – 2024 guideline on behalf of ERKNet, ERA and ESPN
  8. Cystinosis metabolic bone disease: inflammatory profile in human peripheral blood mononuclear cells and derived osteoclasts
  9. Short Bowel Syndrome Is Not a Contraindication for Kidney Transplantation
  10. Application of the updated International IgA Nephropathy Prediction Tool in children one or two years post-biopsy
  11. Incidence, risk factors, management strategies, and outcomes of antibody-mediated rejection in pediatric kidney transplant recipients—a multicenter analysis of the Cooperative European Paediatric Renal Transplant Initiative (CERTAIN)
  12. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy
  13. Favorable Outcome After Single-kidney Transplantation From Small Donors in Children: A Match-controlled CERTAIN Registry Study
  14. Calcineurin inhibitor‐related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature
  15. Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
  16. Addressing the psychosocial aspects of transition to adult care in patients with cystinosis
  17. Extrarenal complications of cystinosis
  18. Nefrotik Düzey Proteinüri ile Başvurunun Çocukluk Çağı Iga Vasküliti Nefriti Seyrine Etkileri
  19. Rituximab-associated hypogammaglobulinemia in children with idiopathic nephrotic syndrome: results of an ESPN survey
  20. IPNA–ESPN Junior Master Class—a decade of successful continuing education and training in pediatric nephrology
  21. Outcome of infantile nephropathic cystinosis depends on early intervention, not genotype: A multicenter sibling cohort study
  22. Response to Dr. Spizzirri et al
  23. Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study
  24. Application of the International IgA Nephropathy Prediction Tool one or two years post-biopsy
  25. Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry
  26. A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
  27. Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
  28. Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation
  29. Young Adults With Hereditary Tubular Diseases: Practical Aspects for Adult-Focused Colleagues
  30. Managing the Nutritional Requirements of the Pediatric End-Stage Kidney Disease Graduate
  31. Correction to: Cystinosis beyond kidneys: gastrointestinal system and muscle involvement
  32. Mitochondria-targeted CoQ10 loaded PLGA-b-PEG-TPP nanoparticles: Their effects on mitochondrial functions of COQ8B HK-2 cells
  33. Hospitalization following pediatric kidney transplantation: An international comparison among a Canadian pediatric transplant center, North American Pediatric Renal Trials and Collaborative Studies, and Cooperative European Pediatric Renal Transplant I...
  34. Newborn Screening: Review of its Impact for Cystinosis
  35. Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages
  36. Correction to: Impact of coronavirus disease-2019 on pediatric nephrology practice and education: an ESPN survey
  37. Blood filters in children with COVID‐19 and acute kidney injury: A review
  38. A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability
  39. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6 ‐deficient livers by macrophage depletion
  40. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
  41. Impact of coronavirus disease-2019 on pediatric nephrology practice and education: an ESPN survey
  42. Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?
  43. Deubiquitination of proteasome subunits by OTULIN regulates type I IFN production
  44. An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
  45. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature
  46. Acute kidney injury in a patient with COVID-19: Answers
  47. Acute kidney injury in a patient with COVID-19: Questions
  48. Updating the International IgA Nephropathy Prediction Tool for use in children
  49. Long-term renal survival of paediatric patients with lupus nephritis
  50. Favipiravir use in children with COVID-19 and acute kidney injury: is it safe?
  51. Development and testing of an artificial intelligence tool for predicting end-stage kidney disease in patients with immunoglobulin A nephropathy
  52. Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients: a cross-sectional web-based survey
  53. Distal renal tubular acidosis: ERKNet/ESPN clinical practice points
  54. Plasma checkpoint protein levels and galectin-9 in juvenile systemic lupus erythematosus
  55. Clinical practice recommendations for recurrence of focal and segmental glomerulosclerosis/steroid‐resistant nephrotic syndrome
  56. Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience
  57. Quantifying Duration of Proteinuria Remission and Association with Clinical Outcome in IgA Nephropathy
  58. Promoting Breastfeeding and Interaction of Pediatric Associations With Providers of Nutritional Products
  59. Transplantation in pediatric aHUS within the era of eculizumab therapy
  60. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease
  61. Improving treatment decisions using personalized risk assessment from the International IgA Nephropathy Prediction Tool
  62. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases
  63. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement
  64. Nephropathic cystinosis: an update on genetic conditioning
  65. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
  66. Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis
  67. Growth Patterns After Kidney Transplantation in European Children Over the Past 25 Years: An ESPN/ERA-EDTA Registry Study
  68. Sex and age as determinants for high blood pressure in pediatric renal transplant recipients: a longitudinal analysis of the CERTAIN Registry
  69. A rare cause of steroid resistant nephrotic syndrome in a child: Questions
  70. A rare cause of steroid-resistant nephrotic syndrome in a child: Answers
  71. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
  72. The European Society for Paediatric Nephrology study of pediatric renal care in Europe: comparative analysis 1998–2017
  73. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation
  74. Management of bone disease in cystinosis: Statement from an international conference
  75. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
  76. Psychiatric morbidity and different treatment modalities in children with chronic kidney disease
  77. Surgical management of renovascular hypertension in children and young adults: a 13-year experience
  78. Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study
  79. Erratum to ‘Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation’ [Pediatric Neurology 88 (2018) 71–74]
  80. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia
  81. Clinical and histopathological prognostic factors affecting the renal outcomes in childhood ANCA-associated vasculitis
  82. Do not Miss Rare and Treatable Cause of Early-Onset Hemolytic Uremic Syndrome: Cobalamin C Deficiency
  83. Reproducibility of the Oxford classification of immunoglobulin A nephropathy, impact of biopsy scoring on treatment allocation and clinical relevance of disagreements: evidence from the VALidation of IGA study cohort
  84. Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update
  85. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation
  86. Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease
  87. JC polyomavirus replication and associated disease in pediatric renal transplantation: an international CERTAIN Registry study
  88. Outcome of renal transplantation in small infants: a match-controlled analysis
  89. Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis
  90. Incomplete vaccination coverage in European children with end-stage kidney disease prior to renal transplantation
  91. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
  92. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis
  93. Infants Requiring Maintenance Dialysis: Outcomes of Hemodialysis and Peritoneal Dialysis
  94. Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimens
  95. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
  96. Predictors of methotrexate response in Turkish children with oligoarticular and polyarticular juvenile idiopathic arthritis
  97. Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association−European Dialysis and Transplant (ESPN/ERA-ED...
  98. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry
  99. Erratum to: Risk factors for progression in children and young adults with IgA nephropathy: an analysis of 261 cases from the VALIGA European cohort
  100. Traitement par étanercept de cinq cas d’ostéomyélite multifocale chronique récurrente (OMCR) réfractaires
  101. Risk factors for progression in children and young adults with IgA nephropathy: an analysis of 261 cases from the VALIGA European cohort
  102. Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease
  103. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
  104. Gender Disparities in Access to Pediatric Renal Transplantation in Europe: Data From the ESPN/ERA‐EDTA Registry
  105. Controversies and research agenda in nephropathic cystinosis: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
  106. Cytomegalovirus Infection in Pediatric Renal Transplantation and the Impact of Chemoprophylaxis With (Val-)Ganciclovir
  107. Impact of Everolimus and Low-Dose Cyclosporin on Cytomegalovirus Replication and Disease in Pediatric Renal Transplantation
  108. The MEST score provides earlier risk prediction in lgA nephropathy
  109. Etanercept treatment in five cases of refractory chronic recurrent multifocal osteomyelitis (CRMO)
  110. Anti-interleukin 1 treatment in secondary amyloidosis associated with autoinflammatory diseases
  111. Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency
  112. Lupus in a patient with cystinosis: is it drug induced?
  113. Treatment of colchicine-resistant Familial Mediterranean fever in children and adolescents
  114. Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation
  115. Does Lower Urinary Tract Status Affect Renal Transplantation Outcomes in Children?
  116. Disparities in treatment rates of paediatric end-stage renal disease across Europe: insights from the ESPN/ERA-EDTA registry
  117. Bisphosphonates in juvenile dermatomyositis with dystrophic calcinosis
  118. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome
  119. Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments
  120. Nephropathic cystinosis: an international consensus document
  121. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
  122. Demographics of paediatric renal replacement therapy in Europe: a report of the ESPN/ERA–EDTA registry
  123. Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience
  124. Wegener’s Granulomatosis Presenting With an Isolated Paranasal Sinus Involvement in a Child
  125. Post-transplant hypertension in pediatric kidney transplant recipients
  126. Disparities in Policies, Practices and Rates of Pediatric Kidney Transplantation in Europe
  127. QT and JT dispersion and cardiac performance in children with neonatal Bartter syndrome: a pilot study
  128. The CERTAIN Registry: A Novel, Web-Based Registry and Research Platform for Pediatric Renal Transplantation in Europe
  129. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
  130. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience
  131. Molecular characterization of cystinuria in south-eastern European countries
  132. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
  133. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
  134. Genetic basis of cystinosis in Turkish patients: a single-center experience
  135. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
  136. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
  137. Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features
  138. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
  139. Low cortisol levels in active juvenile idiopathic arthritis
  140. Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis
  141. Chronic kidney disease in children in Turkey
  142. Erratum to: Chronic kidney disease in children in Turkey
  143. MEFV mutations in systemic onset juvenile idiopathic arthritis
  144. Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up
  145. Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis
  146. Henoch–Schonlein purpura with high factor VIII levels and deep venous thrombosis: an association or coincidence?
  147. Outcome of Primary Glomerular Disease in Pediatric Renal Transplantation: A Single-Center Experience
  148. Renal Transplantation in Children With Lower Urinary Tract Dysfunction of Different Origin: A Single-Center Experience
  149. Triple Immunosuppression With Tacrolimus in Pediatric Renal Transplantation: Single-Center Experience
  150. Eye involvement in children with primary focal segmental glomerulosclerosis
  151. Effect of carnitine supplementation on cardiac function in hemodialyzed children
  152. Carotid intima–media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery
  153. Acute Tubular Injury Associated with Mesalazine Therapy in an Adolescent Girl with Inflammatory Bowel Disease
  154. Is the CD14 C159T polymorphism effective in the development of secondary amyloidosis in Familial Mediterranean fever?
  155. A patient with hyper-IgD syndrome responding to anti-TNF treatment
  156. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function
  157. A multicenter study of patients with adult-onset Still’s disease compared with systemic juvenile idiopathic arthritis
  158. Apoptosis and proliferation in childhood acute proliferative glomerulonephritis
  159. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
  160. An unusual presentation of classic polyarteritis nodosa in a child
  161. Familial Mediterranean Fever (FMF) in Turkey
  162. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch?Sch�nlein purpura
  163. Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis
  164. Bone mineral density in children with familial Mediterranean fever
  165. Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis
  166. Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?
  167. An unusual pattern of arthritis in a child with Kawasaki syndrome
  168. Silence on clinical fundamentals
  169. Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria
  170. Low serum apolipoprotein AI levels in amyloidosis related to familial Mediterranean fever
  171. The role of apoptosis in childhood Henoch?Schonlein purpura
  172. Questions
  173. Urinary glycosaminoglycans in the course of familial Mediterranean fever
  174. A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis
  175. Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis
  176. MEFV gene mutations in familial Mediterranean fever phenotype II patients with renal amyloidosis in childhood: a retrospective clinicopathological and molecular study
  177. Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
  178. Reduced Tc-99m DMSA uptake in a patient with renal tubular acidosis: Effect of acid-base imbalance
  179. Ataxia and peripheral neuropathy: rare manifestations in Henoch-Schönlein purpura
  180. Pediatric renal transplantation: experience from a center in central Anatolia
  181. Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population
  182. Pulmonary Haemorrhage in a 6-Year-Old Boy with Henoch–Scho¨nlein Purpura
  183. Survey of Factor V Leiden and Prothrombin Gene Mutations in Systemic Lupus Erythematosus
  184. Henoch-Schönlein purpura in Wiskott-Aldrich syndrome
  185. Low Chloride Stimulation of Prostaglandin E2Release and Cyclooxygenase-2 Expression in a Mouse Macula Densa Cell Line
  186. A novel G472R mutation in a Turkish family with X-linked Alport syndrome
  187. Renal involvement in polyarteritis nodosa: evaluation of 26 Turkish children
  188. Langerhans' Cell Histiocytosis: Report of an Atypical Case
  189. Antineutrophil Cytoplasmic Antibodies in Juvenile Chronic Arthritis
  190. Evaluation of tumour necrosis factor alpha, interferon gamma and granulocyte-macrophage colony stimulating factor levels in juvenile chronic arthritis.
  191. Wilms' tumour-associated late nephrotic syndrome responsive to treatment
  192. Renovascular hypertension and prolonged encephalopathy associated with moyamoya disease
  193. Kindler syndrome: Absence of definite ultrastructural feature
  194. Nutritional assessment of children on haemodialysis: value of IGF-I, TNF-&agr; and IL-1beta
  195. Antineutrophil cytoplasmic antibodies in childhood systemic lupus erythematosus
  196. Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome
  197. A candidate gene for familial Mediterranean fever
  198. Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis
  199. A rare cause of acute tubulointerstitial nephritis: Salmonella typhimurium infection
  200. Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family
  201. Plasma lipids and lipoproteins in juvenile chronic arthritis
  202. Comparison of Ceftriaxone versus Cefotaxime for Childhood Upper Urinary Tract Infections
  203. T-cell subsets, interleukin-2 receptor expression and production of interleukin-2 in minimal change nephrotic syndrome
  204. Brown tumour as a complication of secondary hyperparathyroidism in uraemia: A case report
  205. Muscle Ultrasound Evaluation of Patients with Familial Mediterranean Fever Complicated by Myalgia
  206. Cranial nerve involvement in childhood polyarteritis nodosa
  207. Long-Term Follow-Up in Children with Steroid-Resistant Nephrotic Syndrome
  208. Peritoneal Hemosiderosis in Pediatric Patients with Nephrogenic Ascites
  209. Protein C and anti-thrombin III levels in nephrotic syndrome and amyloidosis
  210. Hyperimmunoglobulinaemia D and periodic fever mimicking familial Mediterranean fever in the Mediterranean.
  211. Early onset of stone diseases and primary hyperoxaluria
  212. Carbamazepine induced systemic lupus erythematosus
  213. Turkish Journal of Hematology