Doç. Dr. Dilek Giray

Aprimorando a Avaliação do Edema Pulmonar na Cardiopatia Congênita Pediátrica: O Papel da Ultrassonografia Pulmonar

Arquivos Brasileiros de Cardiologia, 2026

DOI 10.36660/abc.20250322 PMID 42138860 1 citation (Europe PMC) Open-access full textSource: OpenAlex

Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non‐Suppressed TSH

Clinical Endocrinology, 2026

DOI 10.1111/cen.70126 PMID 41800491 Source: OpenAlex

Expression Profile of TGFB1 Gene in Pediatric Patients with Isolated Bicuspid Aortic Valve

Pediatric Cardiology, 2025

DOI 10.1007/s00246-024-03733-0 PMID 39681750 3 citations (Europe PMC) Source: ORCID

Autonomic Disturbances in Children with Nutcracker Syndrome: A Case Control Study

Indian Pediatrics, 2024

DOI 10.1007/s13312-024-3332-8 PMID 39267275 Open-access full textSource: OpenAlex

Comorbidity of behavioral problems and parental acceptance-rejection in children diagnosed with chest discomfort, palpitations, vasovagal syncope, and underlying heart disease: a multiple case-control study

BMC Psychiatry, 2024

DOI 10.1186/s12888-024-05527-3 PMID 38267932 2 citations (Europe PMC) Open-access full textSource: OpenAlex

Behavioural interventions to increase adherence to palivizumab prophylaxis in children with CHD

Cardiology in the Young, 2024

DOI 10.1017/s1047951124024946 PMID 38664919 2 citations (Europe PMC) Source: OpenAlex

Longitudinal Changes in Cardiac Function Based on Serial Tissue Doppler and Doppler Imaging for Patients With Sickle Cell Anemia

Journal of Diagnostic Medical Sonography, 2023

DOI 10.1177/87564793221138581 2 citations (OpenAlex) Source: ORCID

Acute myocarditis following COVID-19 mRNA vaccination: a paediatric case

Cardiology in the Young, 2022

DOI 10.1017/s1047951121004698 PMID 35105392 5 citations (Europe PMC) Source: OpenAlex

Congenital biventricular cardiac diverticula as a part of class III Cantrell’s syndrome: case report

Cardiology in the Young, 2022

DOI 10.1017/s1047951122001238 PMID 35438064 1 citation (Europe PMC) Source: OpenAlex

Cardiovascular anomalies in Seckel syndrome: report of two patients and review of the literature

Cardiology in the Young, 2021

DOI 10.1017/s1047951121003097 PMID 34387179 3 citations (Europe PMC) Source: OpenAlex

Pediatride Güncel Yaklaşımlar-1

Akademisyen Kitabevi eBooks, 2021

DOI 10.37609/akya.725 Source: OpenAlex

Athletes´ Heart: QTc Dispersion and Speckle Tracking Echocardiography

Eastern Journal Of Medicine, 2021

DOI 10.5505/ejm.2021.28034 3 citations (OpenAlex) Open-access full textSource: OpenAlex

A rare coincidence: the long QT syndrome and cardio-facio-cutaneous syndrome

Cardiology in the Young, 2020

DOI 10.1017/s1047951120001808 PMID 32635955 1 citation (Europe PMC) Source: OpenAlex

Are there any novel markers in acute rheumatic fever: neutrophil-to-lymphocyte ratio, platelet-to-lymphocyte ratio, and monocyte-to-lymphocyte ratio

Cardiology in the Young, 2020

DOI 10.1017/s104795112000089x PMID 32364093 13 citations (Europe PMC) Source: ORCID

Prognostic value of whole blood count parameters and echocardiographic findings in infants with hypoxic ischemic encephalopathy

Cukurova Medical Journal, 2020

DOI 10.17826/cumj.645596 Open-access full textSource: ORCID

Down sendromlu hastalarda doğuştan kalp hastalığı: Tek merkez, beş yıllık retrospektif analiz

Mersin Üniversitesi Sağlık Bilimleri Dergisi, 2019

DOI 10.26559/mersinsbd.537332 Open-access full textSource: ORCID

A Rare Complication of Left Atrial Dilatation in Childhood: Vocal Cord Paralysis and Ortner Syndrome

DergiPark (Istanbul University), 2019

Source: OpenAlex

2D-Speckle tracking echocardiography contributes to early identification of impaired left ventricular myocardial function in children with chronic kidney disease

Cardiology in the Young, 2018

DOI 10.1017/s1047951118001397 PMID 30152295 10 citations (Europe PMC) Source: ORCID

Patent duktus arteriozuslu bebeklerde konservatif tedavinin sonuçları

Cukurova Medical Journal, 2018

DOI 10.17826/cumj.340749 Open-access full textSource: ORCID

MicroRNA values in children with rheumatic carditis: a preliminary study

Rheumatology International, 2018

DOI 10.1007/s00296-018-4069-2 PMID 29845432 17 citations (Europe PMC) Source: ORCID

Çocuklarda kardiyak cerrahi sonrası gelişen aritmi sıklığı ve risk faktörleri

Mersin Üniversitesi Sağlık Bilimleri Dergisi, 2018

DOI 10.26559/mersinsbd.354887 Open-access full textSource: ORCID

Prognostic markers in congenital diaphragmatic hernia: Left ventricular diameter and pulmonary hypertension

Pediatrics International, 2018

DOI 10.1111/ped.13464 PMID 29178567 11 citations (Europe PMC) Source: ORCID

Therapeutic hypothermia and myocardium in perinatal asphyxia: a microvolt T-wave alternans and Doppler echocardiography study

Bratislava Medical Journal, 2018

DOI 10.4149/bll_2017_144 PMID 29322810 2 citations (Europe PMC) Open-access full textSource: ORCID

Evaluation of Mean Platelet Volume and Other Complete Blood Count Parameters in Children with Atopic Asthma

Bezmialem Science, 2018

DOI 10.14235/bs.2018.1759 2 citations (OpenAlex) Open-access full textSource: OpenAlex

Can whole-blood parameters be used in follow-up of children with rheumatic valvular heart disease?

Cardiology in the Young, 2017

DOI 10.1017/s1047951116001281 PMID 28462757 4 citations (Europe PMC) Source: ORCID

Çarpıntı, göğüs ağrısı ve senkop yakınmalı çocuklarda holter monitorizasyon sonuçları: Sekiz yıllık deneyim

Mersin üniversitesi sağlık bilimleri dergisi/Mersin üniversitesi sağlık bilimleri dergisi, 2017

DOI 10.26559/mersinsbd.285634 2 citations (OpenAlex) Open-access full textSource: OpenAlex

Fetal tanı alan ve yenidoğan döneminde supraventriküler taşikardi geliştiren intraperikardiyal sol ventrikül duvarına invaze dev rabdomiyomlu bir olgu

Mersin üniversitesi sağlık bilimleri dergisi/Mersin üniversitesi sağlık bilimleri dergisi, 2017

DOI 10.26559/mersinsbd.286070 1 citation (OpenAlex) Open-access full textSource: OpenAlex

Ailevi hipertrofik kardiyomiyopati: MYBPC3 geninde yeni bir mutasyon olan bir olgu

Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology, 2017

Open-access full textSource: OpenAlex

Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene

Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology, 2016

DOI 10.5543/tkda.2016.56267 PMID 28694399 1 citation (Europe PMC) Open-access full textSource: ORCID

Doğumsal Kalp Hastalıkları Sıklığının Risk Gruplarına Göre Dağılımı: Fetal Ekokardiyografik Tarama

DergiPark (Istanbul University)

Source: OpenAlex