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Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2024-06, Vol.134 (2), p.148-152

2024

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Echocardiographic Findings and Correlation with Laboratory Values in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with COVID-19

Pediatric cardiology, 2022-02, Vol.43 (2), p.413-425

2022

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Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2022-07, p.1-5

2022

Volltextzugriff (PDF)

Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2024-06, Vol.134 (2), p.148

2024

Volltextzugriff (PDF)

Transcatheter Ventricular Septal Defect Closure with Lifetech™ Konar-MF Occluder in Infants Under 10 kg with Only Using Venous Access

Pediatric cardiology, 2024-01, Vol.45 (1), p.175-183

2024

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The influence of maternal COVID‐19 on cardiac functions: From fetal life to infancy

Echocardiography (Mount Kisco, N.Y.), 2024-01, Vol.41 (1), p.e15736-n/a

2024

Volltextzugriff (PDF)

Multisystem inflammatory syndrome in children: clinical presentation, management, and short- and long-term outcomes

Clinical rheumatology, 2022-12, Vol.41 (12), p.3807-3816

2022

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Admission and follow-up cardiac magnetic resonance imaging findings in BNT162b2 Vaccine-Related myocarditis in adolescents

Infectious diseases (London, England), 2023-03, Vol.55 (3), p.199-206

2023

Volltextzugriff (PDF)

Investigation of the prevalence of cardiovascular risk factors in obese patients diagnosed with metabolic syndrome in childhood and examination of left ventricular function by echocardiography

Journal of pediatric endocrinology & metabolism : JPEM, 2021-07, Vol.34 (7), p.885

2021

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Therapeutic plasma exchange: A potential management strategy for critically ill MIS-C patients in the pediatric intensive care unit

Transfusion and apheresis science, 2021-06, Vol.60 (3), p.103119-103119, Article 103119

2021

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Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International Journal of Neuroscience, 2022, Vol.ahead-of-print (ahead-of-print), p.1-5

2022

Volltextzugriff (PDF)

Çocukluk çağında çarpıntı yakınması ile başvuranlarda ritim holter monitorizasyon sonuçlarının değerlendirilmesi

Turkish Journal of Pediatric Disease, 2019-08, p.1-8

2019

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Changing Face of Acute Rheumatic Fever in Childhood and Our Clinical Results

Northern Clinics of Istanbul, 2023-01, Vol.10 (2), p.237-247

2023

Volltextzugriff (PDF)

Yenidoğan Servis ve Yoğun Bakım Ünitesinde Tanı Alan Doğumsal Kalp Hastalığı Olgularının Geriye Dönük Değerlendirilmesi

Turkish Journal of Pediatric Disease, 2021-09, p.1-9

2021

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Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Echocardiographic Findings and Correlation with Laboratory Values in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with COVID-19

Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Transcatheter Ventricular Septal Defect Closure with Lifetech™ Konar-MF Occluder in Infants Under 10 kg with Only Using Venous Access

The influence of maternal COVID‐19 on cardiac functions: From fetal life to infancy

Multisystem inflammatory syndrome in children: clinical presentation, management, and short- and long-term outcomes

Admission and follow-up cardiac magnetic resonance imaging findings in BNT162b2 Vaccine-Related myocarditis in adolescents

Investigation of the prevalence of cardiovascular risk factors in obese patients diagnosed with metabolic syndrome in childhood and examination of left ventricular function by echocardiography

Therapeutic plasma exchange: A potential management strategy for critically ill MIS-C patients in the pediatric intensive care unit

Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Çocukluk çağında çarpıntı yakınması ile başvuranlarda ritim holter monitorizasyon sonuçlarının değerlendirilmesi

Changing Face of Acute Rheumatic Fever in Childhood and Our Clinical Results

Yenidoğan Servis ve Yoğun Bakım Ünitesinde Tanı Alan Doğumsal Kalp Hastalığı Olgularının Geriye Dönük Değerlendirilmesi

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