Hasil Pencarian - Figen Dogu

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  1. 1
    Scales of Magt1 Gene: Novel Mutations, Different Presentations

    Scales of Magt1 Gene: Novel Mutations, Different Presentations oleh Sule Haskologlu, Kubra Baskin, Caner Aytekin, Candan Islamoglu, Serdar Ceylaner, Figen Dogu, Nurdan Tacyildiz, Emel Unal, Aydan Ikinciogullari

    Diterbitkan 2022-02-01
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  2. 2
    An Unexpected Infection in Loss-of-Function Mutations in STAT3: Malignant Alveolar Echinococcosis in Liver

    An Unexpected Infection in Loss-of-Function Mutations in STAT3: Malignant Alveolar Echinococcosis in Liver oleh Sule Haskologlu, Figen Dogu, Gulnur Gollu Bahadır, Setenay Akyuzluer, Ergin Ciftci, Demet Altun, Sevgi Keles, Meltem Kologlu, Aydan Ikinciogullari

    Diterbitkan 2020-12-01
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  3. 3
    Effects of Umbilical Cord Management Strategies on Stem Cell Transfusion, Delivery Room Adaptation, and Cerebral Oxygenation in Term and Late Preterm Infants

    Effects of Umbilical Cord Management Strategies on Stem Cell Transfusion, Delivery Room Adaptation, and Cerebral Oxygenation in Term and Late Preterm Infants oleh Emel Okulu, Sule Haskologlu, Deniz Guloglu, Ezgi Kostekci, Omer Erdeve, Begum Atasay, Acar Koc, Feride Soylemez, Figen Dogu, Aydan Ikinciogullari, Saadet Arsan

    Diterbitkan 2022-04-01
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  4. 4
    Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience

    Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience oleh Şule Haskoloğlu, Ayşenur Öztürk, Gökcan Öztürk, Sevgi Kostel Bal, Candan İslamoğlu, Kübra Baskın, Serdar Ceylaner, Lale Tufan Satıroğlu, Figen Doğu, Aydan İkincioğulları

    Diterbitkan 2020-11-01
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  5. 5
    Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations

    Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations oleh Fabien Touzot, Laetitia Kermasson, Laurent Jullien, Despina Moshous, Christelle Ménard, Aydan Ikincioğullari, Figen Doğu, Sinan Sari, Vannina Giacobbi-Milet, Amos Etzioni, Jean Soulier, Arturo Londono-Vallejo, Alain Fischer, Isabelle Callebaut, Jean-Pierre de Villartay, Thierry Leblanc, Caroline Kannengiesser, Patrick Revy

    Diterbitkan 2016-11-01
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  6. 6
    Newborn screening for SCID: the very first prospective pilot study from Türkiye

    Newborn screening for SCID: the very first prospective pilot study from Türkiye oleh Sule Haskologlu, Senem Kocak, Lale Satiroglu Tufan, Fethiye Eken Aksoy, Dilan Bastug, Deniz Aslar Oner, Candan Islamoglu, Kubra Baskin, Saliha Esenboga, Deniz Acican, Serdar Ceylaner, Sukru Nail Guner, Sevgi Keles, Deniz Cagdas, Ismail Reisli, Basak Tezel, Figen Dogu, Ilhan Tezcan, Aydan Ikinciogullari

    Diterbitkan 2024-10-01
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  7. 7
    X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world

    X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world oleh Zeinab A. El-Sayed, Irina Abramova, Juan Carlos Aldave, Waleed Al-Herz, Liliana Bezrodnik, Rachida Boukari, Ahmed Aziz Bousfiha, Caterina Cancrini, Antonio Condino-Neto, Ghassan Dbaibo, Beata Derfalvi, Figen Dogu, J.David M. Edgar, Brian Eley, Rasha Hasan El-Owaidy, Sara Elva Espinosa-Padilla, Nermeen Galal, Filomeen Haerynck, Rima Hanna-Wakim, Elham Hossny, Aydan Ikinciogullari, Ebtihal Kamal, Hirokazu Kanegane, Nadia Kechout, Yu Lung Lau, Tomohiro Morio, Viviana Moschese, Joao Farela Neves, Monia Ouederni, Roberto Paganelli, Kenneth Paris, Claudio Pignata, Alessandro Plebani, Farah Naz Qamar, Sonia Qureshi, Nita Radhakrishnan, Nima Rezaei, Nelson Rosario, John Routes, Berta Sanchez, Anna Sediva, Mikko RJ. Seppanen, Edith Gonzalez Serrano, Anna Shcherbina, Surjit Singh, Sangeetha Siniah, Guiseppe Spadaro, Mimi Tang, Ana Maria Vinet, Alla Volokha, Kathleen E. Sullivan

    Diterbitkan 2019-01-01
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