TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
Topaloglu, A Kemal, O'Rahilly, Stephen, Reimann, Frank, Guclu, Metin, Yalin, Ayse Serap, Kotan, L Damla, Porter, Keith M, Serin, Ayse, Mungan, Neslihan O, Cook, Joshua R, Ozbek, Mehmet N, Imamoglu, Sazi, Akalin, N Sema, Yuksel, Bilgin, Semple, Robert K
Published in Nature genetics (01.03.2009)
Published in Nature genetics (01.03.2009)
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Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism
Topaloglu, A. Kemal, Tello, Javier A, Kotan, L. Damla, Ozbek, Mehmet N, Yilmaz, M. Bertan, Erdogan, Seref, Gurbuz, Fatih, Temiz, Fatih, Millar, Robert P, Yuksel, Bilgin
Published in The New England journal of medicine (16.02.2012)
Published in The New England journal of medicine (16.02.2012)
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Risk factors and outcomes related to intensive care unit admission of children with hematological and solid organ malignancies: single-center experience
Kaya, C., Guzelkucuk, Z., Ozyoruk, D., Ozbek, N., Yarali, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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Idiopathic hypereosinophilic syndrome associated pulmonary hypertension in a child
Akcabelen, Y., Bayhan, T., Cinel, G., Ece, I., Ozbek, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation
Yariz, K.O., Sakalar, Y.B., Jin, X., Hertz, J., Sener, E.F., Akay, H., Özbek, M.N., Farooq, A., Goldberg, J., Tekin, M.
Published in Clinical genetics (01.02.2015)
Published in Clinical genetics (01.02.2015)
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Protective Effect of Lycopene against Radiation-Induced Hepatic Toxicity in Rats
Meydan, D, Gursel, B, Bilgici, B, Can, B, Ozbek, N
Published in Journal of international medical research (01.08.2011)
Published in Journal of international medical research (01.08.2011)
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Clinical comparison of weight- and age-based strategy of dose administration in children receiving intravenous busulfan for hematopoietic stem cell transplantation
Gürlek Gökçebay, D., Azik, F., Ozbek, N., Isik, P., Avci, Z., Tavil, B., Kara, A., Tunc, B.
Published in Pediatric transplantation (01.05.2015)
Published in Pediatric transplantation (01.05.2015)
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Thrombin lag time is increased in children with mild asthma
Koksal, B T, Eker, I, Ozbek, N Y, Dogan, I, Y Ozbek, O
Published in Allergologia et immunopathologia (01.05.2019)
Published in Allergologia et immunopathologia (01.05.2019)
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The effects of vitamin D deficiency on myocardial deformation and functions in patients with β-thalassemia
Yozgat, A. Koca, Azak, E., Kaçar, D., Işık, M., Bilir, O. Arman, Çetin, I., Ozbek, N., Yaralı, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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Isolated extramedullary relapse after hematopoietic stem cell transplantation
Guzelkucuk, Z., Isık, P., Bilir, O. Arman, Kacar, D., Yozgat, A. Koca, Isık, M., Gokcebay, D. Gurlek, Bozkaya, I. Ok, Ozbek, N., Yarali, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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Multiple relapsed acute lymphoblastic leukemia with t(9;13) in a child
Gokcebay, D. Gurlek, Akcabelen, Y., Yozgat, A. Koca, Kacar, D., Bilir, O. Arman, Isik, M., Bozkaya, I. Ok, Ozbek, N., Yarali, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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A girl with SAMD9L mutation presenting with pancytopenia, immunodeficiency and myelodsyplasia
Gokcebay, D. Gurlek, Bajin, I. Yaman, Akcabelen, Y., Yozgat, A. Koca, Bilir, O. Arman, Bozkaya, I. Ok, Yarali, N., Ozbek, N.
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
Published in Hematology, Transfusion and Cell Therapy (01.10.2020)
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Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
PARABOSCHI, E. M., KAYIRAN, S. M., ÖZBEK, N., GÜRAKAN, B., PEYVANDI, F., GUELLA, I., DUGA, S., ASSELTA, R.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.03.2012)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.03.2012)
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