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Cardiac functions in children with steroid‐sensitive nephrotic syndrome

Pediatrics international, 2020-12, Vol.62 (12), p.1364-1368

2020

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Effect of creatine and pioglitazone on Hk-2 cell line cisplatin nephrotoxicity

Renal failure, 2014-08, Vol.36 (7), p.1104-1107

2014

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Nutcracker Syndrome in Children: Role of Doppler Ultrasonographic Indices in Detecting the Pattern of Symptoms

Journal of clinical medicine, 2018-08, Vol.7 (8), p.214

2018

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The role of bioelectrical impedance analysis, NT-ProBNP and inferior vena cava sonography in the assessment of body fluid volume in children with nephrotic syndrome

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2018-01, Vol.38 (1), p.48-56

2018

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Managing recurrent parvovirus B19-associated anemia after a pediatric kidney transplant

Pediatric nephrology (Berlin, West), 2024-05

2024

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MIS-C Treatment: Is glucocorticoid monotherapy enough for mild cases?

The American journal of emergency medicine, 2024-09, Vol.83, p.95-100

2024

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Homozygous M694V as a risk factor for amyloidosis in Turkish FMF patients

Gene, 2012-01, Vol.492 (1), p.285-289

2012

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An Evaluation of Mothers’ Feeding Attitudes and Anxiety in Preschool Children

Namık Kemal tıp dergisi, 2022-03, Vol.10 (1), p.29-36

2022

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Long QT syndrome diagnosed in two sisters with propionic acidemia: a case report

Journal of pediatric endocrinology & metabolism : JPEM, 2017-10, Vol.30 (10), p.1133

2017

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The role of bioelectrical impedance analysis, NT-ProBNP and inferior vena cava sonography in the assessment of body fluid volume in children with nephrotic syndrome

Nefrología, 2018-01, Vol.38 (1), p.48-56

2018

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Evaluation of the risk factors for BK virus‐associated hemorrhagic cystitis in pediatric bone marrow transplantation patients: Does post‐transplantation cyclophosphamide increase the frequency?

Pediatric transplantation, 2023-02, Vol.27 (1), p.e14364-n/a

2023

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An uncommon cause of acute kidney injury in young children: Cystinuria

Journal of pediatric urology, 2013-02, Vol.9 (1), p.e58-e63

2013

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Percutaneous Nephrolithotomy in Children: Lessons Learned in 5 Years at a Single Institution

The Journal of urology, 2007-05, Vol.177 (5), p.1867-1871

2007

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Modified Clavien Classification in Percutaneous Nephrolithotomy: Assessment of Complications in Children

The Journal of urology, 2011, Vol.185 (1), p.264-268

2011

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Hemolytic uremic syndrome outbreak in Turkey in 2011

Turkish journal of pediatrics, 2013-05, Vol.55 (3), p.246-252

2013

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The Role of Alvarado and Pediatric Appendicitis Score in Acute Appendicitis in Children

The journal of pediatric research, 2020-09, Vol.7 (3), p.192-198

2020

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A case of Bartonellosis mimicking systemic lupus erythematosus

European journal of ophthalmology, 2023-11, Vol.33 (6), p.NP41-NP48

2023

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Kidney injury molecule-1 and neutrophil gelatinase associated lipocalin in normoalbuminuric diabetic children

Journal of pediatric endocrinology & metabolism : JPEM, 2016-02, Vol.29 (2), p.145

2016

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Is N-terminal pro-brain natriuretic peptide a reliable marker for body fluid status in children with chronic kidney disease?

Archives of medical science, 2020, Vol.16 (4), p.802-810

2020

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Nephrotic syndrome following hepatitis B vaccination: A 17-year follow-up

Northern Clinics of Istanbul, 2021-01, Vol.8 (2), p.196-198

2021

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Leptin and resistin levels and their relationships with glucose metabolism in children with chronic renal insufficiency and undergoing dialysis

Nephrology (Carlton, Vic.), 2006-06, Vol.11 (3), p.192-196

2006

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Genotype–phenotype associations in WT1 glomerulopathy

Kidney international, 2014-05, Vol.85 (5), p.1169-1178

2014

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A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

Paediatrics and international child health, 2020-01, Vol.40 (1), p.65-68

2020

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Cardiac functions in children with steroid‐sensitive nephrotic syndrome

Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study

Effect of creatine and pioglitazone on Hk-2 cell line cisplatin nephrotoxicity

Nutcracker Syndrome in Children: Role of Doppler Ultrasonographic Indices in Detecting the Pattern of Symptoms

The role of bioelectrical impedance analysis, NT-ProBNP and inferior vena cava sonography in the assessment of body fluid volume in children with nephrotic syndrome

Managing recurrent parvovirus B19-associated anemia after a pediatric kidney transplant

MIS-C Treatment: Is glucocorticoid monotherapy enough for mild cases?

Homozygous M694V as a risk factor for amyloidosis in Turkish FMF patients

An Evaluation of Mothers’ Feeding Attitudes and Anxiety in Preschool Children

Long QT syndrome diagnosed in two sisters with propionic acidemia: a case report

The role of bioelectrical impedance analysis, NT-ProBNP and inferior vena cava sonography in the assessment of body fluid volume in children with nephrotic syndrome

Evaluation of the risk factors for BK virus‐associated hemorrhagic cystitis in pediatric bone marrow transplantation patients: Does post‐transplantation cyclophosphamide increase the frequency?

An uncommon cause of acute kidney injury in young children: Cystinuria

Percutaneous Nephrolithotomy in Children: Lessons Learned in 5 Years at a Single Institution

Modified Clavien Classification in Percutaneous Nephrolithotomy: Assessment of Complications in Children

Hemolytic uremic syndrome outbreak in Turkey in 2011

The Role of Alvarado and Pediatric Appendicitis Score in Acute Appendicitis in Children

A case of Bartonellosis mimicking systemic lupus erythematosus

Kidney injury molecule-1 and neutrophil gelatinase associated lipocalin in normoalbuminuric diabetic children

Is N-terminal pro-brain natriuretic peptide a reliable marker for body fluid status in children with chronic kidney disease?

Kidney transplantation in children and adolescents with C3 glomerulopathy or immune complex membranoproliferative glomerulonephritis: a real-world study within the CERTAIN research network

Nephrotic syndrome following hepatitis B vaccination: A 17-year follow-up

Leptin and resistin levels and their relationships with glucose metabolism in children with chronic renal insufficiency and undergoing dialysis

Genotype–phenotype associations in WT1 glomerulopathy

A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

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