ARTICLES
Original articles
- The role of apoptosis in childhood Henoch–Schonlein purpura
- Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever
- Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children
- Decreased prevalence of atopy in paediatric patients with familial Mediterranean fever
- 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
- The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch–Scho¨ nlein purpura
- Bone mineral density in children with familial Mediterranean fever
- Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis
- Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
- E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
- Turkish FMF Study Group.
- Apoptosis and proliferation in childhood acute proliferative glomerulonephritis
- Mutations in the Wilms’ Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9
- Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function
- Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
- Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
- Novel OCRL1 Mutations in PatientsWith the Phenotype of Dent Disease
- Childhood vasculitides in Turkey: a nationwide survey
- Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)
- Pharmacological renoprotection in children with chronic kidney disease.
- Carotid intima–media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery
- Eye involvement in children with primary focal segmental glomerulosclerosis
- Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
- Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome
- Triple Immunosuppression With Tacrolimus in Pediatric Renal Transplantation: Single-Center Experience
- Outcome of Primary Glomerular Disease in Pediatric Renal Transplantation: A Single-Center Experience
- Evaluation of intima media thickness of the common and internal carotid arteries with infammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis
- Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
- A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis
- Superior consistency of ambulatory blood pressure monitoring in children: implications for clinical trials
- ESCAPE trial
- Strict Blood-Pressure Control and Progression of Renal Failure in Children
- Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression
- Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura
- Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
- Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group
- Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
- The bone and mineral disorder of children undergoing chronic peritoneal dialysis
- The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology Association
- Neuroendocrine immune system in familial mediterranean fever
- Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
- COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
- Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome
- MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis
- Genetic basis of cystinosis in Turkish patients: a single-center experience
- 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
- Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical
- Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children
- Circulating suPAR in Two Cohorts of Primary FSGS
- DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
- Role of CXCR1 (CKR-1) in Inflammation of Experimental Mesangioproliferative Glomerulonephritis
- Genetic screening in adolescents with steroidresistant nephrotic syndrome
- Primary coenzyme Q10 (CoQ10) deficiencies and related nephropathies
- Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience
- NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
- Genotype–phenotype associations in WT1 glomerulopathy
- Post-transplant hypertension in pediatric kidney transplant recipients
- Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
- Diagnostic validity of colchicine in patients with Familial Mediterranean fever
- Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome
- Spectrum of Steroid-Resistant and Congenital Nephrotic Syndrome in Children: The PodoNet Registry Cohort
- Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome
- ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
- Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD
- MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis
- Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
- Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
- Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production
- Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children
- Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease.
- First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients
- Tociluzumab treatment in childhood takayasu arteritis: Case series of four patients and systemic review of the literature
- 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
- Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
- Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
- Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children
- The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis
- Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
- Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
- Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
- Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
- Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years
- Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
- An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues
- Response to Early Coenzyme Q10 Supplementation is not sustained in CoQ10 Deficiency Caused by CoQ2 Mutation
- Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
- CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
- Surgical management of renovascular hypertension in children and young adults: a 13-year experience
- 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
- COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
- Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome
- Genetic aspect of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group
- A homozygous HOXA11 variation as a potential novel cause of autosomal recessive CAKUT.
- Cystinosis beyond kidneys: gastrointestinal system and muscle involvement.
- Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases.
- Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease
- Transplantation in pediatric aHUS within the era of eculizumab therapy
- Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience
- Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group.
- Long term renal survival of pediatric patients with lupus nephritis.
- An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
- A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
- Could plasma based therapies still be considered in ed cases with atypical hemolytic uremic syndrome?
- Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion
- A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability.
- Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
- Mitochondria-Targeted CoQ 10 Loaded PLGA-b-PEG-TPP Nanoparticles: Their Effects on Mitochondrial Functions of COQ8B -/- HK-2 cells.
- Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages
- Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
- Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation.
- Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
- A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature.
- Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
- Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression
- The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study
- Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis
- Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis
- Long‑term kidney follow‑up after pediatric acute kidney support therapy for children less than 15 kg
- The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome
- A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)
- Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring
- Acute kidney injury in children with moderate‑severe COVID‑19 and multisystem inflammatory syndrome in children: a referral center experience
- Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells
- COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much?
- Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
- Management of pediatric hemolytic uremic syndrome.
- Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence
- Variable phenotype and genotype of pediatric patients with HNF1B nephropathy
- Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
- 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
- COVID-19 vaccination among adolescents and young adults with chronic kidney conditions: a single-center experience
Case / Brief Reports
- NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome
- A NOVEL MUTATION OF LAMININ ß-2 GENE IN PIERSON SYNDROME MANIFESTED
- Takayasu arteritis in a 4-year-old girl: case report and brief overview of the pediatric literature
- Bilateral subpleural ectopic brain tissue in a 23-week-old fetus
- Laryngeal Atresia Presenting as Fetal Ascites, Olygohydramnios and Lung Appearance Mimicking Cystic Adenomatoid Malformation in a 25-week-old Fetus With Fraser Syndrome
- Three Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts
- New syndrome – Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing
- Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome
- Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation
- Nephropathic Cystinosis Mimicking Bartter Syndrome
- A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl
- Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
- Behc¸et’s Disease with Severe Arterial Involvement in a Child
- CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent’s disease
- Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis
- BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia
- Lupus in a patient with cystinosis: is it drug induced?
- Gastric duplication cyst in an infant with Finnishtype congenital nephrotic syndrome: concurrence or coincidence?
- A NOVEL WT1 GENE MUTATION IN A NEWBORN INFANT DIAGNOSED WITH DENYS-DRASH SYNDROME
- Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4
- Sibs Diagnosed Prenatally With Situs Inversus Totalis, Renal and Pancreatic Dysplasia, and Cysts: A New Syndrome?
- Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?
- Serum IgD Concentrations in Patients with Ataxia Telangiectasia and with Selective IgA Deficiency
- Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia
- Proteinuria in Frasier Syndrome
- Pulmonary Haemorrhage in a 6-Year-Old Boy with Henoch–Scho¨nlein Purpura
- An unusual cause of acute renal failure: renal lymphoma
- Right atrial thrombosis complicating renal transplantation in a child
- Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers
- Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions
- An unusual fetus with complete absence of thoracic lumbar and sacral vertebrae bilateral renal agenesis VSD meningomyelocele, imperforate anus, and teratoma
- Sino-Pulmonary-Renal disease in a child
- Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
- 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
- C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
- A 13-year-old female with Turner syndrome and achalasia
- An unusual cause of diarrhea in a child with nephrotic syndrome: Questions
- An unusual cause of diarrhea in a child with nephrotic syndrome: Answers
- COVID-19 associated thrombotic microangiopathy
- Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient
Textbook Chapters
- Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Small-Vessel Vasculitides
- Childhood Polyarteritis Nodosa
- Other Forms of Vasculitis
- Takayasu Arteritis
- The Kidney in Mitochondrial Diseases