Makaleler
  1. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
  2. Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
  3. Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years
  4. Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
  5. Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome
  6. An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues
  7. Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression
  8. NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome
  9. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
  10. 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
  11. A NOVEL MUTATION OF LAMININ ß-2 GENE IN PIERSON SYNDROME MANIFESTED
  12. Takayasu arteritis in a 4-year-old girl: case report and brief overview of the pediatric literature
  13. Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children
  14. Bilateral subpleural ectopic brain tissue in a 23-week-old fetus
  15. Laryngeal Atresia Presenting as Fetal Ascites, Olygohydramnios and Lung Appearance Mimicking Cystic Adenomatoid Malformation in a 25-week-old Fetus With Fraser Syndrome
  16. Three Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts
  17. New syndrome – Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing
  18. Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome
  19. Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation
  20. Nephropathic Cystinosis Mimicking Bartter Syndrome
  21. TocilizumabtreatmentinchildhoodTakayasuarteritis:Caseseriesof four patientsandsystematicreviewoftheliterature
  22. A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl
  23. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
  24. Behc¸et’s Disease with Severe Arterial Involvement in a Child
  25. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis
  26. CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent’s disease
  27. Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children
  28. Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis
  29. Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis
  30. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis
  31. Carotid intima–media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery
  32. The bone and mineral disorder of children undergoing chronic peritoneal dialysis
  33. NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
  34. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
  35. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
  36. Supplementary Fig. 1. Homozygosity Mapping and WES identify mutations in genes encoding KEOPS complex proteins (LAGE3, OSGEP, TP53RK, TPRKB) in 30 families with GAMOS.
  37. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
  38. Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Small-Vessel Vasculitides
  39. Childhood Polyarteritis Nodosa
  40. Other Forms of Vasculitis
  41. Takayasu Arteritis
  42. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome
  43. Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical
  44. The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology Association
  45. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia
  46. Bone mineral density in children with familial Mediterranean fever
  47. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Medditerranean fever
  48. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
  49. ResponsetoEarlyCoenzymeQ10SupplementationIsnotSustainedinCoQ10DeficiencyCausedbyCoQ2Mutation
  50. Lupus in a patient with cystinosis: is it drug induced?
  51. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children
  52. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children
  53. Superior consistency of ambulatory blood pressure monitoring in children: implications for clinical trials
  54. Strict Blood-Pressure Control and Progression of Renal Failure in Children
  55. Su Homeostazisine Bağlı Bozukluklar
  56. Evaluation of intima media thickness of the common and internal carotid arteries with inXammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis
  57. Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group
  58. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
  59. Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome
  60. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
  61. Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children
  62. Post-transplant hypertension in pediatric kidney transplant recipients
  63. Gastric duplication cyst in an infant with Finnishtype congenital nephrotic syndrome: concurrence or coincidence?
  64. 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
  65. A NOVEL WT1 GENE MUTATION IN A NEWBORN INFANT DIAGNOSED WITH DENYS-DRASH SYNDROME
  66. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
  67. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
  68. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
  69. Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)
  70. Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome
  71. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
  72. 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
  73. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function
  74. ResponsetoEarlyCoenzymeQ10SupplementationIsnotSustainedinCoQ10DeficiencyCausedbyCoQ2Mutation
  75. Su Dengesi Bozuklukları
  76. SODYUM VE SU DENGESİ
  77. Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4
  78. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
  79. SUPPLEMENTAL INFORMATION
  80. Genetic aspect of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group
  81. Genetic screening in adolescents with steroidresistant nephrotic syndrome
  82. Genotype–phenotype associations in WT1 glomerulopathy
  83. Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
  84. MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis
  85. Human Immunology
  86. Arthritis & Rheumatism
  87. Nefroloji ve Genetik
  88. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
  89. Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts: A New Syndrome?
  90. Novel OCRL1 Mutations in PatientsWith the Phenotype of Dent Disease
  91. Surgical management of renovascular hypertension in children and young adults: a 13-year experience
  92. Apoptosis and proliferation in childhood acute proliferative glomerulonephritis
  93. The role of apoptosis in childhood Henoch–Schonlein purpura
  94. Role of CXCR1 (CKR-1) in Inflammation of Experimental Mesangioproliferative Glomerulonephritis
  95. Role of CXCR1 (CKR-1) in Inflammation of Experimental Mesangioproliferative Glomerulonephritis
  96. Diagnostic validity of colchicine in patients with Familial Mediterranean fever
  97. Clinical and Experimental Rheumatology
  98. Eye involvement in children with primary focal segmental glomerulosclerosis
  99. Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?
  100. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch–Scho¨ nlein purpura
  101. Nephrotic syndrome
  102. Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome
  103. Mutations in the Gene DGKE Cause Glomerular Microangiopathy in humans and mice
  104. Primary coenzyme Q10 (CoQ10) deficiencies and related nephropathies
  105. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
  106. Serum IgD Concentrations in Patients with Ataxia Telangiectasia and with Selective IgA Deficiency
  107. Childhood vasculitides in Turkey: a nationwide survey
  108. Ödem
  109. PROTEİNÜRİ
  110. Proteinürinin Sebepleri
  111. Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia
  112. Proteinuria in Frasier Syndrome
  113. Pediatride Gelişmeler
  114. Pulmonary Haemorrhage in a 6-Year-Old Boy with Henoch–Scho¨nlein Purpura
  115. An unusual cause of acute renal failure: renal lymphoma
  116. Right atrial thrombosis complicating renal transplantation in a child
  117. 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
  118. Decreased prevalence of atopy in paediatric patients with familial Mediterranean fever
  119. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers
  120. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions
  121. An unusual fetus with complete absence of thoracic lumbar and sacral vertebrae bilateral renal agenesis VSD meningomyelocele, imperforate anus, and teratoma
  122. Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD
  123. Sino-Pulmonary-Renal disease in a child
  124. Su dengesi Bozukluları
  125. Circulating suPAR in Two Cohorts of Primary FSGS
  126. Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
  127. Functional analysis of BMP4 mutations identified in pediatric CAKUT patients
  128. 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
  129. Mutations in ANKS6 cause a Nephronophthisis-Like Phenotype with End Stage Renal Disease
  130. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
  131. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
  132. Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura
  133. Familial Mediterranean fever patients homozygous for E148Q variant
  134. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
  135. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
  136. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
  137. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
  138. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis
  139. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience
  140. Neuroendocrine immune system in familial mediterranean fever
  141. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
  142. Genetic basis of cystinosis in Turkish patients: a single-center experience
  143. Triple Immunosuppression With Tacrolimus in Pediatric Renal Transplantation: Single-Center Experience
  144. Outcome of Primary Glomerular Disease in Pediatric Renal Transplantation: A Single-Center Experience
  145. Online Supplement
  146. Spectrum of Steroid-Resistant and Congenital Nephrotic Syndrome in Children: The PodoNet Registry Cohort
  147. Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children
  148. A 13-year-old female with Turner syndrome and achalasia
  149. Familial Mediterranean Fever (FMF) in Turkey
  150. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
  151. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
  152. Mutations in the Wilms’ Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9
  153. First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients
  154. Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production