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Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain

American journal of medical genetics. Part A, 2017-09, Vol.173 (9), p.2494-2499

2017

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Novel EDAR mutation in tooth agenesis and variable associated features

European journal of medical genetics, 2020-09, Vol.63 (9), p.103926-103926, Article 103926

2020

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COVID-19 associated multisystemic inflammatory syndrome in 614 children with and without overlap with Kawasaki disease-Turk MIS-C study group

European journal of pediatrics, 2022-05, Vol.181 (5), p.2031-2043

2022

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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

The journal of clinical endocrinology and metabolism, 2016-01, Vol.101 (1), p.284-292

2016

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Evaluation of 601 children with multisystem inflammatory syndrome (Turk MISC study)

European journal of pediatrics, 2023-12, Vol.182 (12), p.5531-5542

2023

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Mercury intoxication resembling pediatric rheumatic diseases: case series and literature review

Rheumatology international, 2020-08, Vol.40 (8), p.1333-1342

2020

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Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children

Pediatric nephrology (Berlin, West), 2023-07, Vol.38 (7), p.2199-2208

2023

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Endoscopic Retrograde Cholangiopancreatography in Pediatric Patients

Journal of laparoendoscopic & advanced surgical techniques. Part A, 2022-03, Vol.32 (3), p.320

2022

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Youth Suicides in the Second Wave of the Pandemic in Turkiye

Genel tip dergisi, 2024-02, Vol.34 (1), p.83-87

2024

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Assessment of bone turnover markers and bone mineral density in normal short boys

Journal of pediatric endocrinology & metabolism : JPEM, 2015-11, Vol.28 (11-12), p.1321

2015

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Tubulopathy and hepatomegaly in a 2-year-old boy: Answers

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2083-2084

2021

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Tubulopathy and hepatomegaly in a 2-year-old boy: Questions

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2081-2082

2021

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A comparison of intravenous immunoglobulin (2 g/kg totally) and single doses of anti-D immunoglobulin at 50 μg/kg, 75 μg/kg in newly diagnosed children with idiopathic thrombocytopenic purpura: Ankara hospital experience

Blood coagulation & fibrinolysis, 2013-07, Vol.24 (5), p.505-509

2013

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Progressive Multifocal Leukoencephalopathy in Children with Primary and Secondary Immune Deficiency

Pediatric allergy, immunology, and pulmonology, 2021-09, Vol.34 (3), p.109

2021

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SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

The Journal of experimental medicine, 2021-06, Vol.218 (6)

2021

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Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study

Epilepsy research, 2024-09, Vol.205, p.107399, Article 107399

2024

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A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index

Pediatric neurology, 2024-03, Vol.152, p.79-86

2024

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Differences and similarities of multisystem inflammatory syndrome in children, Kawasaki disease and macrophage activating syndrome due to systemic juvenile idiopathic arthritis: a comparative study

Rheumatology international, 2022-05, Vol.42 (5), p.879-889

2022

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Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

Turkish journal of haematology, 2018, Vol.35 (4), p.229-259

2018

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The skills of defibrillation practice and certified life‐support training in the healthcare providers in Turkey

International journal of clinical practice (Esher), 2021-12, Vol.75 (12), p.e14978-n/a

2021

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Comparison of clinical and laboratory features and treatment responses in patients with clinically amyopathic juvenile dermatomyositis and classical juvenile dermatomyositis

International journal of rheumatic diseases, 2023-08, Vol.26 (8), p.1504-1511

2023

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Implementation and Statistical Evaluation of a Web-Based Software for Bone Age Assessment

Journal of medical systems, 2011-12, Vol.35 (6), p.1485-1489

2011

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Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain

Novel EDAR mutation in tooth agenesis and variable associated features

Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis

COVID-19 associated multisystemic inflammatory syndrome in 614 children with and without overlap with Kawasaki disease-Turk MIS-C study group

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Evaluation of 601 children with multisystem inflammatory syndrome (Turk MISC study)

Mercury intoxication resembling pediatric rheumatic diseases: case series and literature review

Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children

Endoscopic Retrograde Cholangiopancreatography in Pediatric Patients

Youth Suicides in the Second Wave of the Pandemic in Turkiye

Assessment of bone turnover markers and bone mineral density in normal short boys

Tubulopathy and hepatomegaly in a 2-year-old boy: Answers

Tubulopathy and hepatomegaly in a 2-year-old boy: Questions

The clinical course of SARS-CoV-2 infection among children with rheumatic disease under biologic therapy: a retrospective and multicenter study

A comparison of intravenous immunoglobulin (2 g/kg totally) and single doses of anti-D immunoglobulin at 50 μg/kg, 75 μg/kg in newly diagnosed children with idiopathic thrombocytopenic purpura: Ankara hospital experience

Progressive Multifocal Leukoencephalopathy in Children with Primary and Secondary Immune Deficiency

SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study

The effect of postoperative ventilation strategies on postoperative complications and outcomes in patients with esophageal atresia: Results from the Turkish Esophageal Atresia Registry

A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index

Differences and similarities of multisystem inflammatory syndrome in children, Kawasaki disease and macrophage activating syndrome due to systemic juvenile idiopathic arthritis: a comparative study

Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

The skills of defibrillation practice and certified life‐support training in the healthcare providers in Turkey

Comparison of clinical and laboratory features and treatment responses in patients with clinically amyopathic juvenile dermatomyositis and classical juvenile dermatomyositis

Implementation and Statistical Evaluation of a Web-Based Software for Bone Age Assessment

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