Metrikler
Yayın
79
Açık Erişim
11
BM Sürdürülebilir Kalkınma Amaçları
Duyurular & Dokümanlar
Tez Dosyaları
Ders Dökümanları
Dosya İndir
Eğitim Bilgileri
1998 - 2002
1998 - 2002Tıpta Yandal Uzmanlık
Hacettepe Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Türkiye
1993 - 1997
1993 - 1997Tıpta Uzmanlık
Hacettepe Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Türkiye
1986 - 1992
1986 - 1992Lisans
Hacettepe Üniversitesi, Tıp Fakültesi, Tıp Pr., Türkiye
Yaptığı Tezler
2002
2002Tıpta Yandal Uzmanlık
6-48 Aylık çocuklarda demir eksikliği anemisinde eritrositoz görülme sıklığı: eski bir parametrenin (RBC) yeniden gözden geçirilmesi
Hacettepe Üniversitesi
1997
1997Tıpta Uzmanlık
talasemili hastalarda gelişen sekonder hemokromatozisin magnetik rezonans görüntüleme yöntemiyle değerlendirilmesi
Hacettepe Üniversitesi
Yabancı Diller
B2 Orta Üstü
B2 Orta Üstüİngilizce
Araştırma Alanları
Sağlık Bilimleri
Akademik Ünvanlar / Görevler
2015 - Devam Ediyor
2015 - Devam EdiyorProf. Dr.
Gazi Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri
Yönetilen Tezler
2023
2023Tıpta Uzmanlık
Tıp Fakültesi Öğrencileri Arasında Talasemi Farkındalık Düzeyi Ve Eğitimin Farkındalığa Olan Etkisinin Araştırılması
Aslan D. (Danışman)
E.KÜRKLÜ(Öğrenci)
2020
2020Tıpta Uzmanlık
Beta-talasemi taşıyıcısı çocuklarda eşlik eden demir eksikliğinin HbA2 düzeyi üzerine etkisi
ASLAN D. (Danışman)
Ş.DEĞERMENCİ(Öğrenci)
2016
2016Tıpta Uzmanlık
Talasemi taşıyıcısı çocuklarda periferik kandaki lenfositlerde comet yöntemiyle genotoksisitenin araştırılması
ASLAN D. (Danışman)
D.KARGIN(Öğrenci)
Makaleler
Tümü (66)
SCI-E, SSCI, AHCI (63)
SCI-E, SSCI, AHCI, ESCI (64)
ESCI (1)
Scopus (64)
TRDizin (9)
Diğer Yayınlar (1)
2025
20251. Neutropenia Through Enhanced Neutrophil Apoptosis and Secondary Necrosis in Wolfram Syndrome 1.
Aslan D., Kayhan H.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, 2025 (SCI-Expanded, Scopus, TRDizin)
2025
20252. Cobalamin J Disorder in a Teenage Boy with Recurrent Abdominal Pain Attacks: A Case Report and Literature Review
ASLAN D., Uctepe E., Yesilyurt A., Esen F. N., Dalglç B.
Molecular Syndromology
, 2025 (SCI-Expanded, Scopus)
2025
20253. DNA damage in children with β-thalassemia minor: genotoxicity assessment by comet assay
Menderes D., EMERCE E., Goktas T., ÇAKMAK G., ASLAN D.
TURKISH JOURNAL OF PEDIATRICS
, cilt.67, sa.1, ss.39-50, 2025 (SCI-Expanded, Scopus, TRDizin)
2024
20244. HbA2 levels in children with β-thalassemia trait associated with iron deficiency: A perspective for pediatricians
Degermenci S., Aslan D.
AMERICAN JOURNAL OF CLINICAL PATHOLOGY
, 2024 (SCI-Expanded, Scopus)
2023
20235. Epistaxis-related hemolacria in a 6-year-old female after midfacial trauma: Epistaxis-related hemolacria
Demirer Çelik M., Aslan D.
Indian Journal of Case Reports , cilt.9, sa.9, 2023 (Hakemli Dergi)
2023
20236. DNAJC21-related thrombocytopenia in a young adult female
Aslan D., Akgün Doğan Ö., Ay B., Çamurdan M. O., Mancılar H., Alanay Y.
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
, cilt.193, sa.2, ss.193-197, 2023 (SCI-Expanded, Scopus)
2022
20227. Peripheral Blood Erythrocyte Parameters in B-Thalassemia Minor with Coexistent Iron Deficiency: Comparisons between Iron-Deficient and -Sufficient Carriers
Aslan D., Degermenci S.
THALASSEMIA REPORTS
, cilt.12, sa.2, ss.34-38, 2022 (ESCI)
2022
20228. Fresh Frozen Plasma Plus Iron Therapy in Congenital Hypotransferrinemia in the Second Decade: A Dynamic Approach to Maintaining Hematological Stability
Aslan D.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.39, sa.1, ss.72-74, 2022 (SCI-Expanded, Scopus, TRDizin)
2021
20219. Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin Deficiency
ASLAN D.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.38, sa.2, ss.161-163, 2021 (SCI-Expanded, Scopus, TRDizin)
2020
202010. Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and beta-thalassemia Carriers
Aslan D.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.42, sa.7, 2020 (SCI-Expanded, Scopus)
2019
201911. Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome
ASLAN D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.36, sa.6, ss.390-393, 2019 (SCI-Expanded, Scopus)
2018
201812. Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes
Tummala H., Collopy L. C., Walne A. J., Ellison A., Cardoso S., Aksu T., et al.
BLOOD
, cilt.132, sa.12, ss.1349-1353, 2018 (SCI-Expanded, Scopus)
2018
201813. Formulas for the Detection beta-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters
Aslan D.
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES
, cilt.10, 2018 (SCI-Expanded, Scopus)
2018
201814. The search for new approaches to treating type 1 plasminogen deficiency
ASLAN D., AKATA R. F.
PEDIATRIC BLOOD & CANCER
, cilt.65, sa.4, 2018 (SCI-Expanded, Scopus)
2018
201815. Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10-year observational follow-up with the effects on hematological parameters and growth
ASLAN D.
PEDIATRIC BLOOD & CANCER
, cilt.65, sa.2, 2018 (SCI-Expanded, Scopus)
2017
201716. Fanconi Anemia: A Rarely Considered Cause of Macrocytosis During Childhood
ASLAN D.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.39, sa.7, ss.570-572, 2017 (SCI-Expanded, Scopus)
2017
201717. Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia
Casini A., Vilar R., Beauverd Y., Aslan D., Devreese K., Mondelaers V., et al.
HAEMOPHILIA
, cilt.23, sa.4, ss.583-589, 2017 (SCI-Expanded, Scopus)
2017
201718. Maternal serum alpha-fetoprotein levels are normal in Fanconi anemia: Can it be a lack of postnatal inhibition of AFP gene resulting in the elevation?
ASLAN D., KARABACAK R. O., Aslan O. D.
PEDIATRIC BLOOD & CANCER
, cilt.64, sa.4, 2017 (SCI-Expanded, Scopus)
2016
201619. Harris Platelet Syndrome in Patients of Non-Indian Origin
ASLAN D.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.38, sa.8, 2016 (SCI-Expanded, Scopus)
2016
201620. Pericardial effusion and cardiac tamponade: a sudden and unexpected deterioration in a newborn in the neonatal intensive care unit
AKTAS S., Gumustas M., Onal E., KULA S., ASLAN D.
TURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
, cilt.24, sa.4, ss.777-778, 2016 (SCI-Expanded, Scopus, TRDizin)
2016
201621. Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis
Boppudi S., Boegershausen N., Hove H. B., Percin E. F., Aslan D., Dvorsky R., et al.
CLINICAL GENETICS
, cilt.90, sa.4, ss.334-342, 2016 (SCI-Expanded, Scopus)
2016
201622. "Silent" beta-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A(2)
ASLAN D.
TURKISH JOURNAL OF PEDIATRICS
, cilt.58, sa.3, ss.305-308, 2016 (SCI-Expanded, Scopus, TRDizin)
2016
201623. Recessive congenital methemoglobinemia in immediate generations
ASLAN D., Turkoz-Sucak G., Percy M. J.
TURKISH JOURNAL OF PEDIATRICS
, cilt.58, sa.1, ss.113-115, 2016 (SCI-Expanded, Scopus, TRDizin)
2015
201524. Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test
ASLAN D., Ameziane N., De Winter J. P.
TURKISH JOURNAL OF PEDIATRICS
, cilt.57, sa.3, ss.282-285, 2015 (SCI-Expanded, Scopus, TRDizin)
2014
201425. Oculoectodermal Syndrome: Report of a New Case With a Broad Clinical Spectrum
ASLAN D., AKATA R. F., Schroeder J., Happle R., Moog U., Bartsch O.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, cilt.164, sa.11, ss.2947-2951, 2014 (SCI-Expanded, Scopus)
2014
201426. The X chromosome: does it have a role in Bloom syndrome, a genomic instability disorder?
Aslan D.
TURKISH JOURNAL OF PEDIATRICS
, cilt.56, sa.3, ss.327-329, 2014 (SCI-Expanded, Scopus)
2014
201427. Leukopenia in Familial Mediterranean Fever: Case Series and Literature Review with Special Emphasis on Pathogenesis
Aslan D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.31, sa.2, ss.120-128, 2014 (SCI-Expanded, Scopus)
2013
201328. Failure or delay in diagnosing Fanconi anemia - a well-defined genetic disorder
Aslan D.
TURKISH JOURNAL OF PEDIATRICS
, cilt.55, sa.4, ss.462-464, 2013 (SCI-Expanded, Scopus)
2013
201329. Use of Serum Iron Status and Hemoglobin A2 Levels for Discrimination Between Iron Deficiency and Thalassemia Minor
Aslan D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.30, sa.2, ss.113-115, 2013 (SCI-Expanded, Scopus)
2012
201230. Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenita
ASLAN D., AKATA R. F., Holme H., Vulliamy T., Dokal I.
International Ophthalmology
, cilt.32, sa.6, ss.615-622, 2012 (Scopus)
2012
201231. The MEFV gene and clonal myeloid disorders
Aslan D.
TURKISH JOURNAL OF PEDIATRICS
, cilt.54, sa.5, ss.558-560, 2012 (SCI-Expanded, Scopus)
2011
201132. Familial Mediterranean fever with a single MEFV mutation: can a deletion resulting in alpha-thalassemia be the cause?
Aslan D.
JOURNAL OF HUMAN GENETICS
, cilt.56, sa.2, ss.169-171, 2011 (SCI-Expanded, Scopus)
2011
201133. A665G Mutation in PRF1 in a Turkish Infant With Familial Hemophagocytic Lymphohistiocytosis
Aslan D.
PEDIATRIC BLOOD & CANCER
, cilt.56, sa.2, ss.319-320, 2011 (SCI-Expanded, Scopus)
2010
201034. Dyskeratosis congenita and limbal stem cell deficiency
Aslan D., Akata R. F.
EXPERIMENTAL EYE RESEARCH
, cilt.90, sa.3, ss.472-473, 2010 (SCI-Expanded, Scopus)
2009
200935. The Gene of Bloom's Syndrome: An Autosomal Recessive Disorder with Male Dominance
ASLAN D., EZGÜ F. S.
GENETIC TESTING AND MOLECULAR BIOMARKERS
, cilt.13, sa.4, ss.443-444, 2009 (SCI-Expanded, Scopus)
2009
200936. Dyskeratosis Congenita With Corneal Limbal Insufficiency
ASLAN D., ÖZDEK Ş., Camurdan O., BİDECİ A., CİNAZ P.
PEDIATRIC BLOOD & CANCER
, cilt.53, sa.1, ss.95-97, 2009 (SCI-Expanded, Scopus)
2009
200937. Emperipolesis in immune thrombocytopenic purpura
Aslan D.
INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY
, cilt.52, sa.2, ss.289-290, 2009 (SCI-Expanded, Scopus)
2008
200838. The mode of inheritance' in differentiation of Fanconi anemia from Dyskeratosis congenita
Aslan D.
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL
, cilt.13, sa.11, 2008 (SCI-Expanded, Scopus)
2008
200839. NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I
Percy M. J., Aslan D.
JOURNAL OF CLINICAL PATHOLOGY
, sa.10, ss.1122-1123, 2008 (SCI-Expanded, Scopus)
2008
200840. Automated blood counts and identification of thalassemia carriers
Asian D.
JOURNAL OF POSTGRADUATE MEDICINE
, cilt.54, sa.3, ss.242-243, 2008 (SCI-Expanded, Scopus)
2008
200841. Dysplasia and disorder of cell membrane entirety in iron-deficiency anemia
Yetgin S., ASLAN D., ÜNAL S., Tavil B., KUŞKONMAZ B. B., Elmas S. A., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.25, sa.6, ss.492-501, 2008 (SCI-Expanded, Scopus)
2007
200742. A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene
ASLAN D., Crain K., Beutler E.
ACTA HAEMATOLOGICA
, cilt.118, sa.4, ss.244-247, 2007 (SCI-Expanded, Scopus)
2006
200643. Fanconi anemia (FA) and squamous cell carcinoma in childhood
Aslan D.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
, cilt.70, sa.11, ss.1995-1997, 2006 (SCI-Expanded, Scopus)
2006
200644. Griscelli syndrome: Description of a case with Rab27A mutation
Aslan D., Sari S., Derinoz O., Dalgic B.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.23, sa.3, ss.255-261, 2006 (SCI-Expanded, Scopus)
2005
200545. Gastric angiodysplasia in a child with Bernard-Soulier syndrome: efficacy of octreotide in long-term management.
Kaya Z., Gursel T., Dalgic B., Aslan D.
Pediatric hematology and oncology
, cilt.22, sa.3, ss.223-7, 2005 (SCI-Expanded, Scopus)
2005
200546. Autoimmune thrombocytopenic purpura and Helicobacter pylori infection effectivity during childhood
Yetgin S., DEMİR H. B., Arslan D., Ünal S., Koçak N.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.78, sa.4, ss.318, 2005 (SCI-Expanded, Scopus)
2005
200547. An unusual ocular manifestation in Fanconi anemia: Congenital glaucoma
Aslan D., Ozdogan S., Onol M., Kaya Z., Gursel T.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.78, sa.1, ss.64-66, 2005 (SCI-Expanded, Scopus)
2004
200448. Temporary dysplastic hematological features due to iron deficiency in a case of Poland syndrome
Aslan D., Balci S.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.8, ss.711-715, 2004 (SCI-Expanded, Scopus)
2004
200449. Parvovirus 1319 infection presenting as pre-B-cell acute lymphoblastic leukemia:: A transient and progressive course in two children
Yetgin S., Çetin M., Aslan D., Özyürek E., Anlar B., Uçkan D.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.26, sa.10, ss.689-692, 2004 (SCI-Expanded, Scopus)
2004
200450. Supernumerary nipples in children with hematologic disorders
Aslan D., Gursel T., Kaya Z.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.5, ss.461-463, 2004 (SCI-Expanded, Scopus)
2004
200451. Metamizole sodium-induced severe aplastic anemia and its recovery with a short-course steroid therapy
Yetgin S., Ozyurek E., Aslan D., Cetin M.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.4, ss.343-347, 2004 (SCI-Expanded, Scopus)
2004
200452. Red blood cell count and rapid discrimination between thalassemia trait and iron deficiency anemia
Aslan D.
PEDIATRICS INTERNATIONAL
, cilt.46, sa.3, ss.384, 2004 (SCI-Expanded, Scopus)
2004
200453. The prognosis and survival of childhood acute lymphoblastic leukemia with central nervous system relapse
ÜNAL S., Yetgin S., Cetin M., Gumruk F., Arslan D., Ozyurek E., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.3, ss.279-289, 2004 (SCI-Expanded, Scopus)
2004
200454. Early-onset drusen in a girl with bloom syndrome: probable clinical importance of an ocular manifestation.
Aslan D., Ozturk G., Kaya Z., Bideci A., Ozdogaan S., Gursel T.
Journal of pediatric hematology/oncology
, cilt.26, sa.4, ss.256-7, 2004 (SCI-Expanded, Scopus)
2004
200455. Parvovirus B19 infection associated with severe aplastic anemia in an immunocompetent patient
Yetgin S., Çetin M., Özyürek E., Aslan D., ÇETİNKAYA F. D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.3, ss.223-226, 2004 (SCI-Expanded, Scopus)
2004
200456. Children with acute myeloblastic leukemia presenting with extramedullary infiltration: The effects of high-dose steroid treatment
Hiçsönmez G., Çetin M., TUNCER A., Yenicesu I., Aslan D., Özyürek E., et al.
Leukemia Research
, cilt.28, sa.1, ss.25-34, 2004 (SCI-Expanded, Scopus)
2003
200357. Primary hemophagocytic lymphohistiocytosis in Turkish children
Gurgey A., Gogus S., Ozyurek E., Aslan D., Gumruk F., Cetin M., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.20, sa.5, ss.367-371, 2003 (SCI-Expanded, Scopus)
2003
200358. The role of short course of high-dose methylprednisolone in children with acute myeloblastic leukemia (FAB M2) presented with myeloid tumor
Hicsonmez G., Cetin M., Aslan D., Ozyurek E.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.20, sa.5, ss.373-379, 2003 (SCI-Expanded, Scopus)
2003
200359. Trauma as a risk factor for thrombosis in children: a report of three cases.
Ozyürek E., Beşbaş N., Aslan D., Gürgey A.
The Turkish journal of pediatrics
, cilt.45, sa.2, ss.167-9, 2003 (SCI-Expanded, Scopus)
2003
200360. Incidence of high erythrocyte count in infants and young children with iron deficiency anemia: Re-evaluation of an old parameter
Aslan D., Altay C.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.25, sa.4, ss.303-306, 2003 (SCI-Expanded, Scopus)
2003
200361. Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up
Yetgin S., Tuncer M., Cetin M., Gumruk F., Yenicesu I., Tunc B., et al.
LEUKEMIA
, cilt.17, sa.2, ss.328-333, 2003 (SCI-Expanded, Scopus)
2002
200262. Serum α-fetoprotein level in Fanconi's anemia: Evaluation of 33 Turkish patients
Aslan D., GÜMRÜK F., ALİKAŞİFOĞLU M., Altay Ç.
American Journal of Hematology
, cilt.71, sa.4, ss.275-278, 2002 (SCI-Expanded, Scopus)
2002
200263. Virus-associated immune thrombocytopenic purpura in childhood
Yenicesu I., Yetgin S., Ozyurek E., Aslan D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.19, sa.6, ss.433-437, 2002 (SCI-Expanded, Scopus)
2002
200264. Importance of RDW value in differential diagnosis of hypochrome anemias
Aslan D., Gumruk F., Gurgey A., Altay C.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.69, sa.1, ss.31-33, 2002 (SCI-Expanded, Scopus)
2001
200165. Outcome of noncatheter-related thrombosis in children: Influence of underlying or coexisting factors
Gurgey A., Aslan D.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.23, sa.3, ss.159-164, 2001 (SCI-Expanded, Scopus)
2000
200066. Pseudomonas sepsis with neutrophagocytosis in a premature newborn
Aliefendioglu D., Aslan D., Tekinalp G., Gürgey A.
TURKISH JOURNAL OF PEDIATRICS
, cilt.42, sa.4, ss.328-330, 2000 (SCI-Expanded, Scopus, TRDizin)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2025
20251. Our Personalized Treatment Approach in an Ultra-Rare Disease (Atransferrinemia): Long-Term Outcomes
Aslan D.
EHA 2025, Milan, İtalya, 12 - 15 Haziran 2025, ss.2-4, (Özet Bildiri)
2024
20242. BİR MUTASYON 3 KLİNİK: CTLA-4 HAPLOYETMEZLİĞİNİN AYNI AİLEDE FARKLI YÜZLERİ
ÇAVDAR Z., BASKIN A. K., HASKOLOĞLU Z. Ş., DOĞU E. F., İKİNCİOĞULLARI K. A., ASLAN D.
30. Uluslararası Katılımlı Ulusal Alerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 27 Kasım - 01 Aralık 2024, (Özet Bildiri)
2024
20243. MANY FACES OF CTLA4 HAPLOINSUFFICIENCY
ÇAVDAR Z., BASKIN A. K., HASKOLOĞLU Z. Ş., DOĞU E. F., İKİNCİOĞULLARI K. A., ASLAN D.
21st BIENNIAL MEETING OF THE EUROPEAN SOCIETY FOR IMMUNODEFICIENCY, Fransa, 16 - 19 Ekim 2024, (Özet Bildiri)
2022
20224. USP9X-related intellectual disability in a female with anemia: further delineation of phenotype or dual diagnosis?
Ay B., Akgül T., AKGÜN DOĞAN Ö., ASLAN D., ALANAY Y.
11th Conference on Rare and Undiagnosed Diseases, Vienna, Avusturya, 7 - 08 Kasım 2022, (Tam Metin Bildiri)
2021
20215. Kalıtsal Antitrombin Eksikliği: Ulusal Verilerimiz
ÜNÜVAR A., SARPER N., DEMİRSOY U., EROĞLU N., EKER İ., KAYA Z., et al.
13. Ulusal Pediatrik Hematoloji Kongresi, Antalya, Türkiye, 14 - 17 Ekim 2021, ss.38-39, (Özet Bildiri)
2021
20216. Miks Anemilerin Eritrosit Parametreleri Üstüne Etkisi
UYSAL A. E., ASLAN D.
56. Türk Pediatri Kongresi, Antalya, Türkiye, 17 Ekim 2021, (Tam Metin Bildiri)
2020
20207. 8p 11.2 delesyonu: FGFR1 ve ANK1 komşu gen sendromu
Bideci A., Döğer E., Küpçü Z., Aslan D., Arhan E., Perçin F. E., et al.
XXIV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Ankara, Türkiye, 30 Ekim - 01 Kasım 2020, cilt.1, sa.1, ss.205, (Özet Bildiri)
2017
20178. Genotoxicity assessment of children with B-thalassemia minor by use of micronucleus assay in peripheral blood lymphocytes
Özel Babacanoğlu E., Emerce E., Kargın D., Arslan U., Aslan D., Çakmak G.
2nd International Gazi Pharma Symposium, Ankara, Türkiye, 11 - 13 Ekim 2017, (Özet Bildiri)
2017
20179. Genotoxicity Assessment of Children with Β-Thalassemia Minor by Use of Micronucleus Assay in Peripheral Blood Lymphocytes
Özel Babacanoğlu E., EMERCE GÜRSEL E., Kargın D., ARSLAN U., ASLAN D., ÇAKMAK G.
2nd International Gazi Pharma Symposium Series (GPSS-2017), Ankara, Türkiye, 11 - 13 Ekim 2017, ss.181, (Özet Bildiri)
2016
201610. Bardet Biedl Sendromu Tip 7’de Büyüme Hormonu Eksikliği
KILINÇ UĞURLU A., ASLAN D., DÖĞER E., DEMET AKBAŞ E., BİDECİ A., ÇAMURDAN M. O., et al.
20.ULUSAL PEDİATRİK ENDOKRİNOLOJİ ve DİYABET KONGRESİ, Antalya, Türkiye, 6 - 09 Ekim 2016, (Özet Bildiri)
2013
201311. Yenidoğanlarda Santral Venöz Katater İlişkili Yaşamı Tehdit Eden Komplikasyonlar
GÜMÜŞTAŞ M., KULA S., TOKGÖZ S., Aktaş S., ASLAN D., ÖNAL E. E.
12. Ulusal Pediatrik Kardiyoloji ve Kalp Damar Cerrahisi Kongresi, Türkiye, 1 - 05 Mayıs 2013, (Özet Bildiri)
Kitaplar
2012
20121. Eye Disorders Caused by Limbal Stem Cell Deficiency
Aslan D., Akata R. F.
Stem Cells and Cancer Stem Cells, M.A. Hayat, Editör, Springer, London/Berlin , New Jersey, ss.173-188, 2012
Desteklenen Projeler
2014 - 2017
2014 - 2017Talasemi Taşıyıcılarında Periferik Kandaki Lenfositlerde DNA Hasarının Comet Assay Yöntemi İle Araştırılması
Yükseköğretim Kurumları Destekli Proje , BAP Doktora
ASLAN D. (Yürütücü)
2007 - 2009
2007 - 2009Solid Tümörlü Erişkin Hastalarda Fanconi Anemia (FA) Görülme Sıklığı
Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi
ASLAN D. (Yürütücü)
Bilimsel Yayınlarda Hakemlikler
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Temmuz 2025
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Şubat 2025
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Ocak 2025
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Oturum Başkanı
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Davetli Konuşmacı
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Atıflar
Toplam Atıf Sayısı (WOS): 589
h-indeksi (WOS): 13
Jüri Üyelikleri
Temmuz-2025
Temmuz 2025Akademik Kadroya Atama-Profesörlük
Profesörlük kadrosuna başvurusu dosyası değerlendirme jüriliği - Başkent Üniversitesi
Mart-2022
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Funda Tayfun Küpesiz - Doçentlik Sınav Jürisi, Üniversitelerarası Kurul, Mart 2022. - Gazi Üniversitesi
Mart-2022
Mart 2022