Outcomes of long term treatments of type I hereditary angioedema in a Turkish family
Akoglu, Gulsen, Kesim, Belgin, Yildiz, Gokhan, Metin, Ahmet
Published in Anais brasileiros de dermatología (01.09.2017)
Published in Anais brasileiros de dermatología (01.09.2017)
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Bernard Lerer: recipient of the 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine (Pacific Rim Association for Clinical Pharmacogenetics)
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Published in Omics (Larchmont, N.Y.) (01.04.2014)
Published in Omics (Larchmont, N.Y.) (01.04.2014)
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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene
Büyüköztürk, Suna, MD, Eroğlu, Belgin Kesim, MD, Gelincik, Asl, MD, Üzümcü, Abdullah, PhD, Özşeker, Ferhan, MD, Çolakoğlu, Bahattin, MD, Dal, Murat, MD, Uyguner, Z. Oya, PhD
Published in Journal of allergy and clinical immunology (01.04.2009)
Published in Journal of allergy and clinical immunology (01.04.2009)
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The Turkish Hereditary Angioedema Pilot Study (TURHAPS): The First Turkish Series of Hereditary Angioedema
Kesim, Belgin, Uyguner, Zehra Oya, Gelincik, Aslı, Mete Gökmen, Nihal, Sin, Aytül Z., Karakaya, Gül, Erdenen, Füsun, Ardeniz, Ömür, Özşeker, Ferhan, Gülbahar, Okan, Çolakoğlu, Bahattin, Dal, Murat, Büyüköztürk, Suna
Published in International archives of allergy and immunology (01.01.2011)
Published in International archives of allergy and immunology (01.01.2011)
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Molecular Analysis of Factor V Leiden, Factor V Hong Kong, Factor II G20210A, Methylenetetrahydrofolate Reductase C677T, and A1298C Mutations Related to Turkish Thrombosis Patients
Dölek, Bilgen, Eraslan, Serpil, Eroğlu, Sevim, Kesim, Belgin Eroglu, Ulutin, Turgut, Yalçıner, Altan, Laleli, Yahya R., Gözükirmızı, Nermin
Published in Clinical and applied thrombosis/hemostasis (01.10.2007)
Published in Clinical and applied thrombosis/hemostasis (01.10.2007)
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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age
Saygili, Emre Sedar, Ozturk, Feyza Yener, Sen, Esra Cil, Erol, Rumeysa Selvinaz, Kesim, Belgin Eroglu, Basmaz, Seda Erem, Cakir, Sezin Dogan, Batman, Adnan, Altuntas, Yuksel
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Novel ubiquitin protein ligase E3 component N-Recognin 1 gene mutation in johanson–blizzard syndrome: Development of hypothyroidism during infancy
Celik, Muhittin, Bulbul, Ali, Kirbiyik, Özgür, Kesim, Belgin, Uslu, Sinan, Sukalo, Maja, Zenker, Martin
Published in Journal of clinical neonatology (01.07.2017)
Published in Journal of clinical neonatology (01.07.2017)
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Letter to the editor: A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene
Buyukozturk, Suna, Eroglu, Belgin Kesim, Gelincik, Asli, Uzumcu, Abdullah, Ozseker, Ferhan, Colakoglu, Bahattin, Dal, Murat, Uyguner, Z Oya
Published in Journal of allergy and clinical immunology (01.04.2009)
Published in Journal of allergy and clinical immunology (01.04.2009)
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An Appeal to the Global Health Community for a Tripartite Innovation: An "Essential Diagnostics List," "Health in All Policies," and "See-Through 21(st) Century Science and Ethics"
Dove, Edward S, Barlas, I Ömer, Birch, Kean, Boehme, Catharina, Borda-Rodriguez, Alexander, Byne, William M, Chaverneff, Florence, Coşkun, Yavuz, Dahl, Marja-Liisa, Dereli, Türkay, Diwakar, Shyam, Elbeyli, Levent, Endrenyi, Laszlo, Eroğlu-Kesim, Belgin, Ferguson, Lynnette R, Güngör, Kıvanç, Gürsoy, Ulvi, Hekim, Nezih, Huzair, Farah, Kaushik, Kabeer, Kickbusch, Ilona, Kıroğlu, Olcay, Kolker, Eugene, Könönen, Eija, Lin, Biaoyang, Llerena, Adrian, Malhan, Faruk, Nair, Bipin, Patrinos, George P, Şardaş, Semra, Sert, Özlem, Srivastava, Sanjeeva, Steuten, Lotte M G, Toraman, Cengiz, Vayena, Effy, Wang, Wei, Warnich, Louise, Özdemir, Vural
Published in Omics (Larchmont, N.Y.) (01.08.2015)
Published in Omics (Larchmont, N.Y.) (01.08.2015)
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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age
Emre Sedar Saygılı, Feyza Yener Öztürk, Esra Çil Şen, Erol, Rümeysa Selvinaz, Belgin Eroğlu Kesim, Basmaz, Seda Erem, Sezin Doğan Çakır, Batman, Adnan, Altuntaş, Yüksel
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene
Büyüköztürk, Suna, Eroğlu, Belgin Kesim, Gelincik, Asli, Uzümcü, Abdullah, Ozşeker, Ferhan, Colakoğlu, Bahattin, Dal, Murat, Uyguner, Z Oya
Published in The Journal of allergy and clinical immunology (01.04.2009)
Published in The Journal of allergy and clinical immunology (01.04.2009)
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Roberts - SC fokomeli sendromunun prenatal tanısı: Olgu sunumu
DAVAS, İnci, BAŞARAN, Seher, KESİM, Belgin, Eroğlu, AĞAR, Eser, VAROLAN, Ahmet, YAZGAN, Ali
Published in Perinatoloji dergisi (2006)
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Published in Perinatoloji dergisi (2006)
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Derin ven trombozu ve tekrarlayan gebelik kayıplarında faktör V Leiden ve metilentetrahidrofolat redüktaz C677T mutasyonları: İki olgu sunumu
DAVAS, İnci, AKYOL, Atıf, KESİM, Belgin, Eroğlu, ÇINAR, Sultan, BAKSU, Başak, DÖLEK, Bilgen
Published in Perinatoloji dergisi (2004)
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Published in Perinatoloji dergisi (2004)
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