COVID-19 Interview: Dr. Belgin Eroğlu Kesim on Women in Science Advancing SARS-CoV-2 Tests—“One Health” and Changing the World for the Better von Eroglu Kesim, Belgin, Ozdemir, Vural

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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene von 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

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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 21st Century Science and Ethics”... von Dove, Edward S., Barlas, İ. 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

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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 Pharmacogen... von Özdemir, Vural, Endrenyi, Laszlo, Aynacıoğlu, Şükrü, Bragazzi, Nicola Luigi, Dandara, Collet, Dove, Edward S., Ferguson, Lynnette R., Geraci, Christy Jo, Hafen, Ernst, Kesim, Belgin Eroğlu, Kolker, Eugene, Lee, Edmund J.D., LLerena, Adrian, Nacak, Muradiye, Shimoda, Kazutaka, Someya, Toshiyuki, Srivastava, Sanjeeva, Tomlinson, Brian, Vayena, Effy, Warnich, Louise, Yaşar, Ümit

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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 von Dölek, Bilgen, Eraslan, Serpil, Eroğlu, Sevim, Kesim, Belgin Eroglu, Ulutin, Turgut, Yalçıner, Altan, Laleli, Yahya R., Gözükirmızı, Nermin

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Gene symbol: SERPING1. Disease: Angioneurotic oedema von Uyguner, Zehra Oya, Kesim, Belgin Eroğlu

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Gene symbol: SERPING1. Disease: Angioneurotic oedema von Uyguner, Zehra Oya, Kesim, Belgin Eroğlu

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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age von 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

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Letter to the editor: A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene von Buyukozturk, Suna, Eroglu, Belgin Kesim, Gelincik, Asli, Uzumcu, Abdullah, Ozseker, Ferhan, Colakoglu, Bahattin, Dal, Murat, Uyguner, Z Oya

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Gene symbol: SERPING1. Disease: Angioneurotic oedema von Uyguner, Zehra Oya, Kesim, Belgin Eroğlu

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Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age von 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

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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”... von Dove, Edward S., Barlas, İ. 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

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Gene symbol: SERPING1. Disease: Angioneurotic oedema von Uyguner, Zehra Oya, Kesim, Belgin Eroğlu

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Gene symbol: SERPING1. Disease: Angioneurotic oedema von Uyguner, Zehra Oya, Kesim, Belgin Eroğlu

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A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene von Büyüköztürk, Suna, Eroğlu, Belgin Kesim, Gelincik, Asli, Uzümcü, Abdullah, Ozşeker, Ferhan, Colakoğlu, Bahattin, Dal, Murat, Uyguner, Z Oya

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Roberts - SC fokomeli sendromunun prenatal tanısı: Olgu sunumu von DAVAS, İnci, BAŞARAN, Seher, KESİM, Belgin, Eroğlu, AĞAR, Eser, VAROLAN, Ahmet, YAZGAN, Ali

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Derin ven trombozu ve tekrarlayan gebelik kayıplarında faktör V Leiden ve metilentetrahidrofolat redüktaz C677T mutasyonları: İki olgu sunumu von DAVAS, İnci, AKYOL, Atıf, KESİM, Belgin, Eroğlu, ÇINAR, Sultan, BAKSU, Başak, DÖLEK, Bilgen

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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" von 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

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