Dr. Öğr. Üyesi Eyyüp Yürektürk

Yayın Ağı

Makaleler 11

1. Serum Prolidase and Ischemia-Modified Albumin Levels in Neural Tube Defects: A Comparative Study of Myelomeningocele, Meningocele, and Myeloschisis

Zengin R., Akyol M. E., Arslan M., Arabacı Ö., Yürektürk E., Çetin E., et al.

Medical Science Monitor , cilt.31, 2025 (SCI-Expanded, Scopus)

2. Investigation of the relationship among the anatomical level of the lesion, hydrocephalus and Chiari type 2 pathologies in myelomeningocele patients

Zengin İ., Akyol M. E., Yürektürk E., Çetin E.

Asian Journal of Surgery , 2025 (SCI-Expanded, Scopus)

3. Analysis of Thyroid Hormones in Newborns with Hypoxic Ischaemic Encephalopathy

Aycan N., Yürektürk E., Başaranoğlu M., Karaman S., Demir D. Ç., Tuncer O.

Van Medical Journal , cilt.32, sa.4, ss.246-252, 2025 (Scopus, TRDizin)

4. Role of Netrin-1 in staging hypoxic ischemic encephalopathy

Aycan N., Demir D. Ç., Yürektürk E., Başaranoğlu M., Karaman S., Tuncer O.

Revista da Associacao Medica Brasileira , cilt.71, sa.5, 2025 (SCI-Expanded, Scopus)

5. Correlation of Transfontanel Ultrasonography and Brain Magnetic Resonance Imaging Measurements in Neonates with Hydrocephalus

Aycan N., Arslan H., Yürektürk E., Başaranoğlu M., Ates A., Karaman S., et al.

Turkish Neurosurgery , cilt.35, sa.5, ss.694-700, 2025 (SCI-Expanded, Scopus)

6. İndirekt Hiperbilirubinemili Term Yenidoğanların Etiyolojik Değerlendirmesi

BASARANOGLU M., BATU U., AYCAN N., YUREKTURK E., KARAMAN S., TUNCER O.

Dicle Tıp Dergisi , cilt.51, sa.3, ss.305-313, 2024 (TRDizin)

7. Case Series: 11 Cases of Hemolytic Disease of The Fetus And Newborn Due to Kell Blood Group Incompatibility

Yürektürk E., Aycan N., Başaranoğlu M., Arslan B., Tuncer O.

Eastern Journal of Medicine , cilt.29, sa.4, ss.462-466, 2024 (Scopus, TRDizin)

8. Oxidative and Antioxidative Biomarker Profiles in Neonatal Hypoxic-Ischemic Encephalopathy: Insights for Pathophysiology and Treatment Strategies

Aycan N., Demir D. Ç., Yürektürk E., Başaranoğlu M., Karaman S., Tuncer O.

Medical Science Monitor , cilt.30, 2024 (SCI-Expanded, Scopus)

9. Carotid Intima-Media Thickness and Lipid Profile In Children Patients With Hypothyroidism

Çetin M., Eren A., Bitkin E. Ç., Yürektürk E., Göya C., Karaman K.

Eastern Journal of Medicine , cilt.27, sa.4, ss.552-557, 2022 (Scopus, TRDizin)

10. Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann's thrombasthenia living in Eastern Turkey

Karaman K., Yürektürk E., Geylan H., Yasar A. S., Karaman S., Aymelek H. S., et al.

PLATELETS , cilt.32, ss.238-242, 2021 (SCI-Expanded, Scopus)

11. Wiskott-Aldrich syndrome: Two case reports with a novel mutation.

Kamuran K., ÇETIN M., GEYLAN H., KARAMAN S., DEMIR N., YUREKTURK E., et al.

Pediatric hematology and oncology , cilt.34, ss.286-291, 2017 (SCI-Expanded)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 1

1. wiscott aldrich syndrome: new mutaiton in two cases

Karaman K., yürektürk e., Geylan H., Çetin M., Yavuz İ. H.

3.erciyes pediyatri akademisi kış kongresi, Kayseri, Türkiye, 3 - 10 Eylül 2017, ss.1, (Özet Bildiri)

Metrikler

Dr. Öğr. Üyesi Eyyüp Yürektürk

Yayınlar & Eserler

1. Serum Prolidase and Ischemia-Modified Albumin Levels in Neural Tube Defects: A Comparative Study of Myelomeningocele, Meningocele, and Myeloschisis

2. Investigation of the relationship among the anatomical level of the lesion, hydrocephalus and Chiari type 2 pathologies in myelomeningocele patients

3. Analysis of Thyroid Hormones in Newborns with Hypoxic Ischaemic Encephalopathy

4. Role of Netrin-1 in staging hypoxic ischemic encephalopathy

5. Correlation of Transfontanel Ultrasonography and Brain Magnetic Resonance Imaging Measurements in Neonates with Hydrocephalus

6. İndirekt Hiperbilirubinemili Term Yenidoğanların Etiyolojik Değerlendirmesi

7. Case Series: 11 Cases of Hemolytic Disease of The Fetus And Newborn Due to Kell Blood Group Incompatibility

8. Oxidative and Antioxidative Biomarker Profiles in Neonatal Hypoxic-Ischemic Encephalopathy: Insights for Pathophysiology and Treatment Strategies

9. Carotid Intima-Media Thickness and Lipid Profile In Children Patients With Hypothyroidism

10. Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann's thrombasthenia living in Eastern Turkey

11. Wiskott-Aldrich syndrome: Two case reports with a novel mutation.

1. wiscott aldrich syndrome: new mutaiton in two cases

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Yayın (WoS)

Yayın (Scopus)

Atıf (Scopus)

H-İndeks (Scopus)

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