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Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

American journal of human genetics, 2014-12, Vol.95 (6), p.637-648

2014

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Childhood urinary tract infection caused by extended‐spectrum β‐lactamase‐producing bacteria: Risk factors and empiric therapy

Pediatrics international, 2017-02, Vol.59 (2), p.176-180

2017

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Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

Pediatric nephrology (Berlin, West), 2018-03, Vol.33 (3), p.473-483

2018

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Is neutrophil-to-lymphocyte ratio valid to predict organ involvement in Henoch–Schönlein purpura?

Rheumatology international, 2016-08, Vol.36 (8), p.1147-1148

2016

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A Case of Liddle Syndrome: Correspondence

Indian journal of pediatrics, 2014-11, Vol.81 (11), p.1278-1278

Ekinci, Zelal

2014

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Successful treatment of macrophage activation syndrome due to systemic onset juvenile idiopathic arthritis with antithymocyte globulin

Rheumatology international, 2015-10, Vol.35 (10), p.1779-1780

2015

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Early Bone Marrow Failure in a 6-Year-Old Boy with Cystinosis

Pediatric hematology and oncology, 2015-04, Vol.32 (3), p.212-214

2015

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Refractory idiopathic recurrent pericarditis: treatment with interleukin-1 receptor antagonist is an option

Journal of cardiovascular medicine (Hagerstown, Md.), 2017-09, Vol.18 (9), p.731

2017

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Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review

Rheumatology international, 2020-11, Vol.40 (11), p.1903-1910

2020

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Can serum amyloid a level be used to support the Familial Mediterranean Fever diagnosis?

Pediatric rheumatology online journal, 2014-09, Vol.12 (S1), p.P245-P245, Article P245

2014

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Effect of cholecalciferol on local arterial stiffness and endothelial dysfunction in children with chronic kidney disease

Pediatric nephrology (Berlin, West), 2016-02, Vol.31 (2), p.267-277

2016

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Monitoring of Adverse Events and Safety in Autoinflammatory Diseases: Real-Life Data from the Eurofever Registry

Journal of clinical immunology, 2024-06, Vol.44 (5), p.119, Article 119

2024

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Childhood urinary tract infection caused by extended-spectrum [beta]-lactamase-producing bacteria: Risk factors and empiric therapy

Pediatrics international, 2017-02, Vol.59 (2), p.176

2017

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Urinary Tract Infection Prophylaxis in Children with Neurogenic Bladder with Cranberry Capsules : Randomized Controlled Trial

ISRN pediatrics, 2012, Vol.2012 (2012), p.1-4

2012

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A case of SCNN1A splicing mutation presenting as mild systemic pseudohypoaldosteronism type 1

Journal of Pediatric Endocrinology and Metabolism, 2013-11, Vol.26 (11), p.1197-1200

2013

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Comparison of the efficacy of once- and twice-daily colchicine dosage in pediatric patients with familial Mediterranean fever--a randomized controlled noninferiority trial

Arthritis research & therapy, 2016-04, Vol.18 (85), p.85-85, Article 85

2016

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Congenital Anomalies of Kidney and Urinary Tract (CAKUT): Single Center Experience for 14 Years

Güncel pediatri, 2019-04, Vol.17 (1), p.45-57

2019

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Hemolytic uremic syndrome outbreak in Turkey in 2011/Reply

Turkish journal of pediatrics, 2013-11, Vol.55 (6), p.667

2013

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Hemolytic uremic syndrome outbreak in Turkey in 2011 - Reply

Turkish journal of pediatrics, 2013-11, Vol.55 (6), p.668-668

2013

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Macrophage activation syndrome due to systemic onset juvenile idiopathic arthritis in a case with liver transplantation

Pediatric rheumatology online journal, 2014-09, Vol.12 (S1), p.P223-P223, Article P223

2014

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Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation

Turkish journal of pediatrics, 2012-03, Vol.54 (2), p.168-170

2012

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Renal outcome with eculizumab in two diarrhea-associated hemolytic–uremic syndrome cases with severe neurologic involvement

Hong Kong journal of nephrology, 2014-10, Vol.16 (2), p.46-49

2014

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A rare presentation of systemic lupus erythematosus: diffuse alveolar hemorrhage in an infant

Pediatric rheumatology online journal, 2014-09, Vol.12 (S1), p.P315-P315, Article P315

2014

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Retrospective Assessment of Children with Henoch-Schonlein Purpura in and around Kocaeli Province and Comparison with Literature

Erciyes tip dergisi, 2014, Vol.36 (2), p.62-67

2014

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A Rare Cause of Acute Renal Damage Followed by an Initial Diagnosis of STEC HUS: Rhabdomyolysis: Case Report

Turkiye Klinikleri Journal of Pediatrics, 2015, Vol.24 (4), p.160-163

2015

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Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

Childhood urinary tract infection caused by extended‐spectrum β‐lactamase‐producing bacteria: Risk factors and empiric therapy

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

Is neutrophil-to-lymphocyte ratio valid to predict organ involvement in Henoch–Schönlein purpura?

A Case of Liddle Syndrome: Correspondence

Successful treatment of macrophage activation syndrome due to systemic onset juvenile idiopathic arthritis with antithymocyte globulin

Early Bone Marrow Failure in a 6-Year-Old Boy with Cystinosis

Refractory idiopathic recurrent pericarditis: treatment with interleukin-1 receptor antagonist is an option

Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review

Can serum amyloid a level be used to support the Familial Mediterranean Fever diagnosis?

Effect of cholecalciferol on local arterial stiffness and endothelial dysfunction in children with chronic kidney disease

Monitoring of Adverse Events and Safety in Autoinflammatory Diseases: Real-Life Data from the Eurofever Registry

Childhood urinary tract infection caused by extended-spectrum [beta]-lactamase-producing bacteria: Risk factors and empiric therapy

Urinary Tract Infection Prophylaxis in Children with Neurogenic Bladder with Cranberry Capsules : Randomized Controlled Trial

A case of SCNN1A splicing mutation presenting as mild systemic pseudohypoaldosteronism type 1

Comparison of the efficacy of once- and twice-daily colchicine dosage in pediatric patients with familial Mediterranean fever--a randomized controlled noninferiority trial

Congenital Anomalies of Kidney and Urinary Tract (CAKUT): Single Center Experience for 14 Years

Hemolytic uremic syndrome outbreak in Turkey in 2011/Reply

Hemolytic uremic syndrome outbreak in Turkey in 2011 - Reply

Macrophage activation syndrome due to systemic onset juvenile idiopathic arthritis in a case with liver transplantation

Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation

Renal outcome with eculizumab in two diarrhea-associated hemolytic–uremic syndrome cases with severe neurologic involvement

A rare presentation of systemic lupus erythematosus: diffuse alveolar hemorrhage in an infant

Retrospective Assessment of Children with Henoch-Schonlein Purpura in and around Kocaeli Province and Comparison with Literature

A Rare Cause of Acute Renal Damage Followed by an Initial Diagnosis of STEC HUS: Rhabdomyolysis: Case Report

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