ARTICLES


Original articles

  1. The role of apoptosis in childhood Henoch–Schonlein purpura
  2. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever
  3. Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children
  4. Decreased prevalence of atopy in paediatric patients with familial Mediterranean fever
  5. Influence Of Serum Amyloid A(SAA1) and SAA2 Gene Polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the turkish population
  6. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch–Scho¨ nlein purpura
  7. Bone mineral density in children with familial Mediterranean fever
  8. Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis
  9. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
  10. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
  11. Turkish FMF Study Group.
  12. Apoptosis and proliferation in childhood acute proliferative glomerulonephritis
  13. Mutations in the Wilms’ Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9
  14. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function
  15. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
  16. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
  17. Novel OCRL1 Mutations in PatientsWith the Phenotype of Dent Disease
  18. Childhood vasculitides in Turkey: a nationwide survey
  19. Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)
  20.  Pharmacological renoprotection in children with chronic kidney disease
  21. Carotid intima–media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery
  22. Eye involvement in children with primary focal segmental glomerulosclerosis
  23. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
  24. Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome
  25. Triple Immunosuppression With Tacrolimus in Pediatric Renal Transplantation: Single-Center Experience
  26. Outcome of Primary Glomerular Disease in Pediatric Renal Transplantation: A Single-Center Experience
  27. Evaluation of intima media thickness of the common and internal carotid arteries with infammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis
  28. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
  29. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis
  30. Superior consistency of ambulatory blood pressure monitoring in children: implications for clinical trials
  31. ESCAPE trial
  32. Strict Blood-Pressure Control and Progression of Renal Failure in Children
  33. Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression
  34. Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura
  35. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
  36. Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group
  37. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
  38. The bone and mineral disorder of children undergoing chronic peritoneal dialysis
  39. The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology Association
  40. Neuroendocrine immune system in familial mediterranean fever
  41. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
  42. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
  43. Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome
  44. MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis
  45. Genetic basis of cystinosis in Turkish patients: a single-center experience
  46. Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability
  47. Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical
  48. Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children
  49. Circulating suPAR in Two Cohorts of Primary FSGS
  50. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
  51. Role of CXCR1 (CKR-1) in Inflammation of Experimental Mesangioproliferative Glomerulonephritis
  52. Genetic screening in adolescents with steroidresistant nephrotic syndrome
  53. Primary coenzyme Q10 (CoQ10) deficiencies and related nephropathies
  54. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience
  55. NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
  56. Genotype–phenotype associations in WT1 glomerulopathy
  57. Post-transplant hypertension in pediatric kidney transplant recipients
  58. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
  59. Diagnostic validity of colchicine in patients with Familial Mediterranean fever
  60. Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome
  61. Spectrum of Steroid-Resistant and Congenital Nephrotic Syndrome in Children: The PodoNet Registry Cohort
  62. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome
  63. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
  64. Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD
  65. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis
  66. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
  67. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
  68. Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production
  69. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children
  70. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease.
  71. First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients
  72. Tociluzumab treatment in childhood takayasu arteritis: Case series of four patients and systemic review of the literature
  73. 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
  74. Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
  75. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
  76. Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children
  77. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis
  78. Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
  79. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
  80. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
  81. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
  82. Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years
  83. Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
  84. An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues
  85. Response to Early Coenzyme Q10 Supplementation is not sustained in CoQ10 Deficiency Caused by CoQ2 Mutation
  86. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
  87. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
  88. Surgical management of renovascular hypertension in children and young adults: a 13-year experience
  89. 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
  90. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
  91. Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome
  92. Genetic aspect of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group
  93. A homozygous HOXA11 variation as a potential novel cause of autosomal recessive CAKUT.
  94. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement.
  95. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases.
  96. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease
  97. Transplantation in pediatric aHUS within the era of eculizumab therapy
  98. Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience
  99. Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group.
  100.  Long term renal survival of pediatric patients with lupus nephritis. 
  101.  An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
  102. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
  103. Could plasma based therapies still be considered in ed cases with atypical hemolytic uremic syndrome?
  104. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion
  105. A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability.
  106. Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
  107. Mitochondria-Targeted CoQ 10 Loaded PLGA-b-PEG-TPP Nanoparticles: Their Effects on Mitochondrial Functions of COQ8B -/- HK-2 cells.
  108. Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages
  109. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. 
  110. Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation.
  111. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
  112.  A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature.
  113. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
  114. Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression 
  115. The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study
  116. Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis
  117. Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis
  118. Long‑term kidney follow‑up after pediatric acute kidney support therapy for children less than 15 kg
  119. The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome
  120. A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)
  121. Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring
  122. Acute kidney injury in children with moderate‑severe COVID‑19 and multisystem inflammatory syndrome in children: a referral center experience
  123. Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells
  124. COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much?
  125. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
  126. Management of pediatric hemolytic uremic syndrome.
  127. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence

 

Case / Brief Reports

  1. NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome
  2. A NOVEL MUTATION OF LAMININ ß-2 GENE IN PIERSON SYNDROME MANIFESTED
  3. Takayasu arteritis in a 4-year-old girl: case report and brief overview of the pediatric literature
  4. Bilateral subpleural ectopic brain tissue in a 23-week-old fetus
  5. Laryngeal Atresia Presenting as Fetal Ascites, Olygohydramnios and Lung Appearance Mimicking Cystic Adenomatoid Malformation in a 25-week-old Fetus With Fraser Syndrome
  6. Three Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts
  7. New syndrome – Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing
  8. Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome
  9. Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation
  10. Nephropathic Cystinosis Mimicking Bartter Syndrome
  11. A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl
  12. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
  13. Behc¸et’s Disease with Severe Arterial Involvement in a Child
  14. CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent’s disease
  15. Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis
  16. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia
  17. Lupus in a patient with cystinosis: is it drug induced?
  18. Gastric duplication cyst in an infant with Finnishtype congenital nephrotic syndrome: concurrence or coincidence?
  19. A NOVEL WT1 GENE MUTATION IN A NEWBORN INFANT DIAGNOSED WITH DENYS-DRASH SYNDROME
  20. Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4
  21. Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts: A New Syndrome?
  22. Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?
  23. Serum IgD Concentrations in Patients with Ataxia Telangiectasia and with Selective IgA Deficiency
  24. Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia
  25. Proteinuria in Frasier Syndrome
  26. Pulmonary Haemorrhage in a 6-Year-Old Boy with Henoch–Scho¨nlein Purpura
  27. An unusual cause of acute renal failure: renal lymphoma
  28. Right atrial thrombosis complicating renal transplantation in a child
  29. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers
  30. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions
  31. An unusual fetus with complete absence of thoracic lumbar and sacral vertebrae bilateral renal agenesis VSD meningomyelocele, imperforate anus, and teratoma
  32. Sino-Pulmonary-Renal disease in a child
  33. Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
  34. A Case Report of Thrombocytopenia-associated Multiple Organ Failure Secondary to Salmonella enterica Serotype Typhi Infection in a Pediatric Patient: Successful Treatment With Plasma Exchange
  35. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
  36. A 13-year-old female with Turner syndrome and achalasia
  37. An unusual cause of diarrhea in a child with nephrotic syndrome: Questions
  38. An unusual cause of diarrhea in a child with nephrotic syndrome: Answers
  39. COVID-19 associated thrombotic microangiopathy
  40. Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient

 

Textbook Chapters

  1. Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Small-Vessel Vasculitides
  2. Childhood Polyarteritis Nodosa
  3. Other Forms of Vasculitis
  4. Takayasu Arteritis
  5. The Kidney in Mitochondrial Diseases

 

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