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Digestion of Chromatin in Apoptotic Cell Microparticles Prevents Autoimmunity

Cell, 2016-06, Vol.166 (1), p.88-101

2016

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Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

BMC nephrology, 2017-01, Vol.18 (1), p.6-6, Article 6

2017

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Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years

Nephron (2015), 2018-01, Vol.139 (3), p.211-218

2018

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Management of antenatal hydronephrosis

Pediatric nephrology (Berlin, West), 2020-12, Vol.35 (12), p.2231-2239

2020

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DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome

Arthritis & rheumatology (Hoboken, N.J.), 2013-08, Vol.65 (8), p.2183-2189

2013

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The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study

Nephron (2015), 2024, Vol.148 (5), p.319-332

2024

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Anti-IL-1 treatment in familial Mediterranean fever and related amyloidosis

Clinical rheumatology, 2016-02, Vol.35 (2), p.441-446

2016

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An infant with severe refractory Crohn’s disease and homozygous MEFV mutation who dramatically responded to colchicine

Rheumatology international, 2012-03, Vol.32 (3), p.783-785

2012

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Prevalence of Hypertension in Children with Early-Stage ADPKD

Clinical journal of the American Society of Nephrology, 2018-06, Vol.13 (6), p.874-883

2018

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High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT

Pediatric nephrology (Berlin, West), 2013-11, Vol.28 (11), p.2143-2147

2013

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Prevalence of the MEFV Gene Mutations in Childhood Polyarteritis Nodosa

The Journal of pediatrics, 2007-12, Vol.151 (6), p.675-678

2007

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Acute kidney injury in a paediatric intensive care unit: comparison of the pRIFLE and AKIN criteria

Acta Paediatrica, 2012-03, Vol.101 (3), p.e126-e129

2012

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Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation

Pediatric neurology, 2018-11, Vol.88, p.71-74

2018

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Sacroiliitis in Children With Familial Mediterranean Fever

Journal of clinical rheumatology, 2019-03, Vol.25 (2), p.69-73

2019

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Proteinuria in pediatric renal transplant recipients

Pediatric transplantation, 2018-02, Vol.22 (1), p.n/a

2018

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Late-onset disease is associated with a mild phenotype in children with familial Mediterranean fever

Clinical rheumatology, 2016-07, Vol.35 (7), p.1837-1840

2016

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Hypertension and improved left ventricular mass index in children after renal transplantation

Pediatric transplantation, 2017-12, Vol.21 (8), p.n/a

2017

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Neonatal onset familial Mediterranean fever

Modern rheumatology, 2019-07, Vol.29 (4), p.647-650

2019

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Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?

Journal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.46-54

2019

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Childhood polyarteritis nodosa: diagnosis with non-invasive imaging techniques

Clinical rheumatology, 2017, Vol.36 (1), p.165-171

2017

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Hypertension induced reversible posterior leukoencephalopathy syndrome: a report of two cases

European journal of pediatrics, 2004-12, Vol.163 (12), p.728-730

2004

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Vascular comorbidities in familial Mediterranean fever

Rheumatology international, 2011-10, Vol.31 (10), p.1275-1281

2011

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Hypertension in children after renal transplantation

Pediatrics international, 2015-12, Vol.57 (6), p.1138-1142

2015

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Infliximab therapy for familial Mediterranean fever-related amyloidosis: case series with long term follow-up

Clinical rheumatology, 2012-08, Vol.31 (8), p.1267-1271

2012

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Digestion of Chromatin in Apoptotic Cell Microparticles Prevents Autoimmunity

Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years

Management of antenatal hydronephrosis

DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome

The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study

Anti-IL-1 treatment in familial Mediterranean fever and related amyloidosis

An infant with severe refractory Crohn’s disease and homozygous MEFV mutation who dramatically responded to colchicine

Prevalence of Hypertension in Children with Early-Stage ADPKD

High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT

Prevalence of the MEFV Gene Mutations in Childhood Polyarteritis Nodosa

Early Effects of Renal Replacement Therapy on Cardiovascular Comorbidity in Children With End-Stage Kidney Disease: Findings From the 4C-T Study

Acute kidney injury in a paediatric intensive care unit: comparison of the pRIFLE and AKIN criteria

Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation

Sacroiliitis in Children With Familial Mediterranean Fever

Proteinuria in pediatric renal transplant recipients

Late-onset disease is associated with a mild phenotype in children with familial Mediterranean fever

Hypertension and improved left ventricular mass index in children after renal transplantation

Neonatal onset familial Mediterranean fever

Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?

Childhood polyarteritis nodosa: diagnosis with non-invasive imaging techniques

Hypertension induced reversible posterior leukoencephalopathy syndrome: a report of two cases

Vascular comorbidities in familial Mediterranean fever

Hypertension in children after renal transplantation

Infliximab therapy for familial Mediterranean fever-related amyloidosis: case series with long term follow-up

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