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1دورية أكاديمية
المؤلفون: Ruken Yıldırım, Edip Ünal, Şervan Özalkak, Akçahan Akalın, Ayça Aykut, Nevzat Yılmaz
المصدر: JCRPE, Vol 16, Iss 1, Pp 76-83 (2024)
مصطلحات موضوعية: ptpn11, noonan syndrome, short stature, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Deniz Güven, Mustafa Bak, Erkin Serdaroğlu, Ferda Özkınay, Ayça Aykut
المصدر: Journal of Behçet Uz Children's Hospital, Vol 11, Iss 3, Pp 286-294 (2021)
مصطلحات موضوعية: acute post-streptococcal glomerulonephritis, mannose-binding lectin, gene polymorphism, prognosis., Pediatrics, RJ1-570
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Asude Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata, Esra Işık, Damla Gökşen, Özgür Çoğulu, Ferda Özkınay
المصدر: JCRPE, Vol 13, Iss 1, Pp 52-60 (2021)
مصطلحات موضوعية: obesity, hypogonadotropic hypogonadism, carboxypeptidase, carboxypeptidase e, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anıl Korkmaz, Korcan Demir, Behzat Özkan, Özgür Çoğulu
المصدر: JCRPE, Vol 12, Iss 4, Pp 358-365 (2020)
مصطلحات موضوعية: shox gene, short stature, mlpa, sequence analysis, madelung’s deformity, hearing loss, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Melis Kose, Ebru Canda, Mehtap Kagnici, Ayça Aykut, Ogün Adebali, Asude Durmaz, Aylin Bircan, Gulden Diniz, Cenk Eraslan, Engin Kose, Aycan Ünalp, Ünsal Yılmaz, Berk Ozyilmaz, Taha Reşid Özdemir, Tahir Atik, Sema Kalkan Uçar, Robert McFarland, Robert W. Taylor, Garry K. Brown, Mahmut Çoker, Ferda Özkınay
المصدر: Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100657- (2020)
مصطلحات موضوعية: COX deficiency, Leigh syndrome, Neuroregression, Next-generation sequencing, Nuclear mitochondrial disorders, SURF1 gene, Medicine (General), R5-920, Biology (General), QH301-705.5
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Sezer Acar, Hale Tuhan, Korcan Demir, Ayça Aykut, Asude Durmaz, Ünal Utku Karaarslan, Gözde İnci, Oğuz Ateş, Ece Böber, Ayhan Abacı
المصدر: Journal of Pediatric Research, Vol 5, Iss 1, Pp 48-51 (2018)
مصطلحات موضوعية: Pheochromocytoma, von-Hippel Lindau syndrome, hemangioblastoma, Medicine, Pediatrics, RJ1-570
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Emin Karaca, Ayça Aykut, Biray Ertürk, Burak Durmaz, Ahmet Güler, Barış Büke, Ahmet Özgür Yeniel, Ahmet Mete Ergenoğlu, Ferda Özkınay, Mehmet Özeren, Mert Kazandı, Fuat Akercan, Sermet Sağol, Cumhur Gündüz, Özgür Çoğulu
المصدر: Balkan Medical Journal, Vol 35, Iss 2, Pp 163-166 (2018)
مصطلحات موضوعية: Down syndrome, microRNAs, amniotic fluid, Medicine
وصف الملف: electronic resource
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8دورية أكاديمية
المؤلفون: Ayca, Aykut, Lynett, Patrick J.
المصدر: In Ocean Engineering 15 September 2021 236
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9
المؤلفون: Aylin Yüksel Ülker, Dilek Uludağ Alkaya, Ahmet Okay Çağlayan, Esra Usluer, Ayça Aykut, Ayça Aslanger, Mehmet Vural, Beyhan Tüysüz
مصطلحات موضوعية: Genetics, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0174ce25e0b9d47408a7ded67e7dca
https://avesis.deu.edu.tr/publication/details/079fd9bb-1a6d-44c8-8eb6-f38a6f9e25e1/oai -
10
المؤلفون: Burak Deliloğlu, Özlem Tüfekçi, Funda Tüzün, Ayça Aykut, Emine İpek Ceylan, Asude Durmaz, Şebnem Yılmaz, Nuray Duman, Hasan Özkan, Hale Ören
مصطلحات موضوعية: Male, Sanger sequencing, resuscitation, thrombocytopenia, rash, whole exome sequencing, computer assisted tomography, newborn, differential diagnosis, virus infection, echocardiography, Congenital Bone Marrow Failure Syndromes, MECOM protein, human, genetics, gene mutation, gestational age, transcription factor, thorax radiography, clinical article, disseminated intravascular clotting, blood clotting test, phagocytosis, immunosuppressive treatment, laboratory test, hematopoietic stem cell transplantation, MDS1 and EVI1 complex locus protein, Infant, Premature, MECOM gene, bone marrow transplantation, erythroid precursor cell, Article, pancytopenia, fetus hypoxia, case report, follow up, Humans, ecchymosis, Apgar score, human, computed tomographic angiography, cesarean section, flow cytometry, leukopenia, neutrophil count, prematurity, lung malformation, Infant, Newborn, Infant, hemoglobin, platelet count, congenital amegakaryocytic thrombocytopenia, lung hemorrhage, ophthalmology, Pediatrics, Perinatology and Child Health, Mutation, hyperpigmentation, erythrocyte sedimentation rate, neonate, blood cell count, karyotype 46,XY, Transcription Factors
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a01de1225c165d8698f66f14bc6a95
https://avesis.deu.edu.tr/publication/details/6816b441-7341-4947-ae64-d00630bcbf33/oai