Guillain-Barré syndrome in an immunocompromised patient with Wiskott-Aldrich syndrome by Akgün Olmez, Tuba Turul, Ilhan Tezcan, Güzide Turanli

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A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase by Lütfiye Mesci, Hilal Ozdag, Tuba Turul, Fügen Ersoy, Ilhan Tezcan, Ozden Sanal

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Hereditary C1q deficiency: a new family with C1qA deficiency by Cağman Sun-Tan, Tuba Turul Ozgür, Gamze Kilinç, Rezan Topaloğlu, Ozay Gököz, Sibel Ersoy-Evans, Ozden Sanal

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Clinical features of chronic granulomatous disease: a series of 26 patients from a single center by Tuba Turul-Ozgür, Gülten Türkkani-Asal, Ilhan Tezcan, M Yavuz Köker, Ayşe Metin, Leman Yel, Fügen Ersoy, Ozden Sanal

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Mild clinical phenotype and subtle radiographic findings in an infant with cartilage-hair hypoplasia by Gülten Türkkani-Asal, Yasemin Alanay, Tuba Turul-Ozgür, Martin Zenker, Christian Thiel, Anita Rauch, Sule Unal, Aytemiz Gürgey, Ilhan Tezcan

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Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene by Bahar Göktürk, Capucine Picard, Jean-Laurent Casanova, Melanie Migaud, Durmuş Burgucu, Tuba Turul-Özgür, Caroline Deswarte, Carmen Oleaga-Quintas, Ümran Çalışkan, İsmail Reisli, Jacinta Bustamante

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