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
128. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy
129. Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
130. 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
131. COVID-19 vaccination among adolescents and young adults with chronic kidney conditions: a single-center experience

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