Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes
Altuntaş, Cansu, Uzunhan, Tugce Aksu, Ertürk, Biray, Petmezci, Mey Talip, Çakar, Nafiye Emel, Noyan, Bilge, Dokucu, Ali İhsan, Önal, Hasan
Published in Clinical neurology and neurosurgery (01.01.2024)
Published in Clinical neurology and neurosurgery (01.01.2024)
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A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy
Altuntaş, Cansu, Uzunhan, Tugce Aksu, Ertürk, Biray, Petmezci, Mey Talip, Çakar, Nafiye Emel, Noyan, Bilge, Dokucu, Ali İhsan, Önal, Hasan
Published in Clinical neurology and neurosurgery (01.06.2023)
Published in Clinical neurology and neurosurgery (01.06.2023)
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Evaluation of S100A12 protein levels in children with Familial Mediterranean Fever
Türkmenoğlu, Yelda, Güney, Elif, Bezen, Diğdem, irdem, Ahmet, Ertürk, Biray, Dursun, Hasan
Published in Turkish journal of medical sciences (28.06.2021)
Published in Turkish journal of medical sciences (28.06.2021)
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Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome
Aksu Uzunhan, Tuğçe, Ertürk, Biray, Aydın, Kürşad, Ayaz, Akif, Altunoğlu, Umut, Yarar, Murat Hakkı, Gezdirici, Alper, İçağasıoğlu, Dilara Füsun, Gökpınar İli, Ezgi, Uyanık, Bülent, Eser, Metin, Kutbay, Yaşar Bekir, Topçu, Yasemin, Kılıç, Betül, Bektaş, Gonca, Arduç Akçay, Ayfer, Ekici, Barış, Chousein, Amet, Avcı, Şahin, Yüksel, Atıl, Kayserili, Hülya
Published in Clinical neurology and neurosurgery (01.01.2023)
Published in Clinical neurology and neurosurgery (01.01.2023)
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Clinical and Pathological Characteristics of Patients with High-Risk Breast Cancer Based on BRCA Mutation Profiles: A Retrospective Study
Atcı, Muhammed Mustafa, Geredeli, Çağlayan, Ay, Seval, Sakin, Abdullah, Ertürk, Biray, Seçmeler, Şaban, Arıcı, Serdar, Çekin, Ruhper, Yaşar, Nurgül, Can, Orçun, Cihan, Şener, Gümüş, Mahmut
Published in European journal of breast health (01.04.2021)
Published in European journal of breast health (01.04.2021)
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MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome
Karaca, Emin, Aykut, Ayça, Ertürk, Biray, Durmaz, Burak, Güler, Ahmet, Büke, Barış, Yeniel, Ahmet Özgür, Ergenoğlu, Ahmet Mete, Özkınay, Ferda, Özeren, Mehmet, Kazandı, Mert, Akercan, Fuat, Sağol, Sermet, Gündüz, Cumhur, Çoğulu, Özgür
Published in Balkan medical journal (01.03.2018)
Published in Balkan medical journal (01.03.2018)
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Cleidocranial Dysplasia: A New Mutation
Nimet Pınar Yılmazbaş, Bezen, Diğdem, Ertürk, Biray
Published in European Archives of Medical Research (01.12.2019)
Published in European Archives of Medical Research (01.12.2019)
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Evaluation of Laboratory Findings, Clinical Features and Rates of Diagnosis of Patients Admitted to Outpatient Clinic of Pediatric Neurology with Neuromuscular Manifestations
Aksu Uzunhan, Tuğçe, Ertürk, Biray, Özyavuz Çubuk, Pelin, Uyanık, Bülent, Ayaz, Akif, Akan, Onur, Özdemir, Taha Reşid
Published in Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi (01.01.2020)
Published in Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi (01.01.2020)
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Sequencing of mutations in the serine/threonine kinase domain of the bone morphogenetic protein receptor type 2 gene causing pulmonary arterial hypertension
Mutlu, Zeynep, Kayıkçıoğlu, Meral, Nalbantgil, Sanem, Vuran, Özcan, Kemal, Hatice, Moğulkoç, Nesrin, Ertürk, Biray, Onay, Hüseyin, Eroğlu, Zuhal, Kültürsay, Hakan
Published in Anatolian journal of cardiology (01.07.2016)
Published in Anatolian journal of cardiology (01.07.2016)
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Journal Article
Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome
Karaca, Emin, Aykut, Ayça, Ertürk, Biray, Durmaz, Burak, Güler, Ahmet, Büke, Barış, Yeniel, Ahmet Özgür, Ergenoğlu, Ahmet Mete, Özkınay, Ferda, Özeren, Mehmet, Kazandı, Mert, Akercan, Fuat, Sağol, Sermet, Gündüz, Cumhur, Çoğulu, Özgür
Published in Balkan medical journal (15.03.2018)
Published in Balkan medical journal (15.03.2018)
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Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants
Hamanaka, Kohei, Miyake, Noriko, Mizuguchi, Takeshi, Miyatake, Satoko, Uchiyama, Yuri, Tsuchida, Naomi, Sekiguchi, Futoshi, Mitsuhashi, Satomi, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Saitsu, Hirotomo, Yamada, Kohei, Sakamoto, Masamune, Fukuda, Hiromi, Ohori, Sachiko, Saida, Ken, Itai, Toshiyuki, Azuma, Yoshiteru, Koshimizu, Eriko, Fujita, Atsushi, Erturk, Biray, Hiraki, Yoko, Ch'ng, Gaik-Siew, Kato, Mitsuhiro, Okamoto, Nobuhiko, Takata, Atsushi, Matsumoto, Naomichi
Published in Genome medicine (26.04.2022)
Published in Genome medicine (26.04.2022)
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A Rare GCMB Gene Mutation in an Isolated Hypoparathyroidism Case
Ertürk, Biray, Karaca, Emin, Silce, Caroline, Özkinay, Ferda
Published in Journal of clinical research in pediatric endocrinology (01.09.2015)
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Published in Journal of clinical research in pediatric endocrinology (01.09.2015)
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Meme kanseri kök hücrelerinde elajik asit ile indüklenmiş miRNA’ların ifadesi ve elajik asidin apoptoz üzerine etkisi
Çağlar, Hasan Onur, Yılmaz Süslüer, Sunde, Kavaklı, Şebnem, Gündüz, Cumhur, Ertürk, Biray, Özkınay, Ferda, Haydaroğlu, Ayfer
Published in Ege tıp dergisi (01.12.2017)
Published in Ege tıp dergisi (01.12.2017)
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Cyclic manner of neutropenia in a patient with HAX-1 mutation
Cipe, Funda Erol, Celiksoy, Mehmet Halil, Erturk, Biray, Aydogmus, Çiğdem
Published in Pediatric hematology and oncology (20.11.2018)
Published in Pediatric hematology and oncology (20.11.2018)
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Journal Article
A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy
Altuntaş, Cansu, Uzunhan, Tugce Aksu, Ertürk, Biray, Petmezci, Mey Talip, Çakar, Nafiye Emel, Noyan, Bilge, Dokucu, Ali İhsan, Önal, Hasan
Published in Clinical neurology and neurosurgery (01.06.2023)
Published in Clinical neurology and neurosurgery (01.06.2023)
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Prenatal Evaluation of MicroRNA Expressions in Pregnancies with Down Syndrome
Ozkinay, Ferda, Kazandi, Mert, Akercan, Fuat, Sagol, Sermet, Gunduz, Cumhur, Cogulu, Ozgur, Ergenoglu, Ahmet Mete, Yeniel, Ahmet Ozgur, Buke, Baris, Guler, Ahmet, Durmaz, Burak, Aykut, Ayca, Karaca, Emin, Erturk, Biray, Ozeren, Mehmet
Published in BioMed research international (01.01.2016)
Published in BioMed research international (01.01.2016)
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Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation
Ozkinay, Ferda, Onay, Huseyin, Karaca, Emin, Arslan, Esra, Erturk, Biray, Ece Solmaz, Asli, Tekin, Ismihan Merve, Cogulu, Ozgur, Aydinok, Yeşim, Vergin, Canan
Published in Hemoglobin (04.07.2015)
Published in Hemoglobin (04.07.2015)
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