KİŞİSEL BİLGİLER
Adı Soyadı Prof. Dr. Ebru YILMAZ KESKİN
Birimi Tıp Fakültesi
Bölüm Dahili Tıp Bilimleri Bölümü
Ana Bilim Dalı Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
E-Posta E-Posta Adresini Göster
ORCID ID 0000-0002-1462-9876
Akademik Hesaplar image/svg+xml
Bu sayfadaki kişisel verilerin görünürlüğü KVKK 8. madde hükmü uyarınca ilgili kişinin açık rızası kapsamındadır. Kişisel verilerinizin görünürlüğünü veya hali hazırdaki verilerinizi Personel Bilgi Sistemi (PBS) ve Akademik Bilgi Sistemi (ABS) üzerinden düzenleyebilirsiniz.
ÖĞRENİM BİLGİLERİ
Lisans HACETTEPE ÜNİVERSİTESİ TIP (İNGİLİZCE) 30.06.2000
AKADEMİK YAYIN ANALİZLERİ (Son 5 Yıl)
İLGİ ALANLARI
YAYINLAR
  • Uluslararası Hakemli Dergilerde Yayımlanan Makaleler
  • 1 YILMAZ KESKİN EBRU, KESKİN MAHMUT, KARAİBRAHİMOĞLU ADNAN, Association of Maternal Vitamin B12 Status With Infant Findings and Neurodevelopment in Vitamin B12-Deficient Breast-fed Babies. Ovid Technologies (Wolters Kluwer Health), 44(1), , 91-95. Doi: 10.1097/MPH.0000000000002122, (2022), (SCI-Expanded)
  • 2 Fermo Elisa, Vercelatti Cristina, Marcello Anna Paola, YILMAZ KESKİN EBRU, Perrotta Silverio, Zaninoni Anna, Brancaleoni Valentina, Zanella Alberto, Giannotta Juri A., Barcellini Wilma, Bianchi Paola, Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study. Frontiers in Physiology Doi: 10.3389/fphys.2021.684569, (2021), (SCI-Expanded)
  • 3 SALMAN HAKAN, ASLAN VAHİDE NAGEHAN, AKÇAM MUSTAFA, ARSLAN MÜJGAN, AKKUZU EMİNE, YILMAZ KESKİN EBRU, AÇARI CEYHUN, KESKİN MAHMUT, ATAR MÜGE, Köşker Muhammet, SİNANOĞLU MUHAMMED SELÇUK, ÇETİN HASAN, AKÇAM FÜSUN ZEYNEP, COVID-19-associated multisystem inflammatory syndrome in children: Experiences of three centres in Turkey. Modern Rheumatology Doi: 10.1093/mr/roab042, (2021), (SCI-Expanded)
  • 4 YILMAZ KESKİN EBRU, YÜCEER RAMAZAN OĞUZ, BAŞPINAR ŞİRİN, OKUR ERDOĞAN, BERDELİ AFİG, MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura. Journal of Pediatric Hematology/Oncology (2021), (SCI-Expanded)
  • 5 Olgac Asburce, KASAPKARA ÇİĞDEM SEHER, Kilic Mustafa, YILMAZ KESKİN EBRU, SANDAL GONCA, Cram David Stephen, Haberle Johannes, TORUN DENİZ, Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy. JOURNAL OF PEDIATRIC ENDOCRINOLOGY METABOLISM, 33(10), , 1349-1352. (2020), (SCI-Expanded)
  • 6 ÖNER NERGİZ, Gursel Turkiz, KAYA ZÜHRE, YILMAZ KESKİN EBRU, KOÇAK ÜLKER, ALBAYRAK MERYEM, YENİCESU İDİL, BELEN APAK FATMA BURCU, ışık melek, Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study. TRANSFUSION AND APHERESIS SCIENCE (2020), (SCI-Expanded)
  • 7 çakmaklı seda, KAPLAN ÇİĞDEM, uzunoğlu mehmet, büyükbayram merve, Görgülü Emel, Özkan Zarif Nurten, YILMAZ KESKİN EBRU, A novel homozygous nonsense mutation (p.Y78) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings. TURKISH JOURNAL OF PEDIATRICS (2020), (SCI-Expanded)
  • 8 elisabetta valoti, alberti marta, carrara camillo, breno matteo, YILMAZ KESKİN EBRU, bresin elena, cuccarolo paola, acikgöz yonca, benigni ariela, noris marina, remuzzi giuseppe, mele caterina, Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.. NEPHRON (2019), (SSCI)
  • 9 YILMAZ KESKİN EBRU, ACAR ÖZNUR, özbas halil, Missed Diagnosis of β-Thalassemia Trait in Premarital Screening Due to Accompanying HbA2-Yialousa (HBD: c.82GT).. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2019), (SCI-Expanded)
  • 10 Çoban Sümeyra, YILMAZ KESKİN Ebru, İğde Mahir, Association between Maternal and Infantile Markers of Cobalamin Status During the First Month Post-Delivery. The Indian Journal of Pediatrics Doi: 10.1007/s12098-017-2598-4, (2018), (SCI-Expanded)
  • 11 Colakoglu Seyma, BAYHAN TURAN, TAVİL EMİNE BETÜL, YILMAZ KESKİN EBRU, Cakir Volkan, GÜMRÜK FATMA, ÇETİN MUALLA, AYTAÇ EYÜPOĞLU ŞEVKİYE SELİN, BERBER ERGÜL, Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.. Blood transfusion = Trasfusione del sangue , 1-8. Doi: 10.2450/2016.0098-16, (2018), (SCI-Expanded)
  • 12 Kayilioglu Hulya, Kocak Ulker, Karaer Derya Kan, Percin Emriye F., Sal Ertan, Tekkesin Funda, Isik Melek, Oner Nergiz, Belen Fatma B., YILMAZ KESKİN EBRU, OKUR ARZU, ALBAYRAK MERYEM, KAYA ZÜHRE, Pinarli Faruk G., YENİCESU İDİL, KARADENİZ CEYDA, Oğuz Aynur, Gürsel Türkiz, Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 39(6), , 458-462. Doi: 10.1097/MPH.0000000000000910, (2017), (SCI)
  • 13 YILMAZ KESKİN EBRU, Fettah Ali, Oliveira Ana Catarina, Toprak Sule, Lopes Andreia, Bento Celeste, First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey. TURKISH JOURNAL OF HEMATOLOGY, 34(4), , 372-373. Doi: 10.4274/tjh.2017.0213, (2017), (SCI-Expanded)
  • 14 De Falco Luigia, Bruno Mariasole, YILMAZ KESKİN EBRU, Sal Ertan, Buyukavci Mustafa, KAYA ZÜHRE, Girelli Domenico, Iolascon Achille, The role of Matriptase-2 during the early postnatal development in humans. HAEMATOLOGICA, 101(4), Doi: 10.3324/haematol.2015.139808, (2016), (SCI)
  • 15 Sal Ertan, YILMAZ KESKİN EBRU, YENİCESU İDİL, Bruno Mariasole, De Falco Luigia, Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutations. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 33(3), , 226-232. Doi: 10.3109/08880018.2016.1157229, (2016), (SCI)
  • 16 YILMAZ KESKİN EBRU, GÜRSEL TÜRKİZ, KAYA ZÜHRE, LETIAN DAI, KOÇAK ÜLKER, YENİCESU İDİL, BELEN FATMA BURCU, MITCHELL MICHAEL, Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. BLOOD COAGULATION & FIBRINOLYSIS Doi: DOI:10.1097/MBC.0000000000000185, (2015), (SCI-Expanded)
  • 17 YILMAZ KESKİN EBRU, KESKİN MAHMUT, Severe vitamin B₁₂ deficiency in a 15-year-old boy: presentation with haemolysis and pancytopenia.. BMJ case reports Doi: pii: bcr2015209718. 10.1136/bcr-2015-209718, (2015), (Diğer)
  • 18 DE FALCO LUIGIA, SILVESTRI LAURA, KANNENGIESSER CAROLINE, MORAN ERICA, OUDIN CLAIRE, RAUSA MARCO, BRUNO MARIASOLE, ARANDA JESSICA, ARGILES BIENVENIDA, YENİCESU İDİL, FALCON RODRIGUEZ MARIA, YILMAZ KESKİN Ebru, KOÇAK ÜLKER, BEAUMONT CAROLE, CAMASCHELLA CLARA, IOLASCON ACHILLE, GRANDCHAMP BERNARD, SANCHEZ MAYKA, Functional and clinical impact of novel TMPRSS6 variants in iron refractory iron deficiency anemia patients and genotype phenotype studies. HUMAN MUTATION (2014), (SCI-Expanded)
  • 19 BELEN FATMA BURCU, KOÇAK ÜLKER, IŞIK MELEK, YILMAZ KESKİN EBRU, ÖNER NERGİZ, SAL ERTAN, KAYA ZÜHRE, YENİCESU İDİL, GÜRSEL TÜRKİZ, Evaluation of Pediatric Bleeding Questionnaire in Turkish Children With Von Willebrand Disease and Platelet Function Disorders. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS (2014), (SCI-Expanded)
  • 20 YILMAZ KESKİN EBRU, SAL ERTAN, DE FALCO LUIGIA, BRUNO MARIASOLE, IOLASCON ACHILLE, KOÇAK ÜLKER, YENİCESU İDİL, Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations. TURKISH JOURNAL OF PEDIATRICS (2013), (SCI-Expanded)
  • 21 KOÇAK ÜLKER, GÜRSEL TÜRKİZ, KAYA ZÜHRE, ARAL YUSUF ZİYA, ALBAYRAK MERYEM, YILMAZ KESKİN Ebru, BELEN BURCU, IŞIK MELEK, ÖNER NERGİZ, ALL BFM 95 treatment in Turkish children with acute lymphoblastic leukemia experience of a single center. PEDIATRIC HEMATOLOGY AND ONCOLOGY (2012), (SCI-Expanded)
  • 22 ALBAYRAK MERYEM, KAYA ZÜHRE, YILMAZ KESKİN EBRU, ZUR STADT UDO, KOÇAK ÜLKER, GÜRSEL TÜRKİZ, Fatal Epstein Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin 11 mutation. TURKISH JOURNAL OF PEDIATRICS (2009), (SCI-Expanded)
  • 23 YILMAZ KESKİN Ebru, Neonatal tetanus in Turkey what has changed in the last decade. BMC INFECTIOUS DISEASES (2008), (SCI-Expanded)
  • Ulusal Hakemli Dergilerde Yayımlanan Makaleler
  • 1 ÇAKMAK YILMAZ ÖZLEM, YILMAZ KESKİN EBRU, YİĞİTHAN AYHAN, KESKİN MAHMUT, Sudden Onset of Life Threatening Methaemoglobinaemia After Intake of Inappropriately Stored Vegetable Collard Greens Meal in a 2 5 Year Old Child. Cukurova Medical Journal (2015), (Diğer)
  • Kitap
  • 1 YILMAZER YASİN, UYSAL HACER İPEK, YILMAZ KESKİN EBRU, Çocuk Hematolojide Olgularla Akut Lösemiler(2021). Galenos Yayınevi, Bölüm, (ULUSAL)
  • 2 YILMAZ KESKİN EBRU, Sağlıklı Nesil Sağlam Gelecek(2021). S.D.Ü Kitabevi, Bölüm, (ULUSAL)
  • 3 YILMAZ KESKİN EBRU, Sağlıklı Nesil, Sağlam Gelecek(2021). S.D.Ü Kitabevi, Bölüm, (ULUSAL)
 
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