Showing 1 - 4 results of 4 for search 'Ebru Yilmaz-Keskin', query time: 0.01s Refine Results
  1. 1
    Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation

    Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation by Meryem Albayrak, Zühre Kaya, Ebru Yilmaz-Keskin, Udo Zur Stadt, Ulker Koçak, Türkiz Gürsel

    Published 2009-08-01
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  2. 2
    A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings

    A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings by Seda Çakmaklı, Çiğdem Kaplan, Mehmet Uzunoğlu, Merve Büyükbayram, Emel Görgülü, Nurten Özkan Zarif, Ebru Yılmaz Keskin

    Published 2020-02-01
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  3. 3
    Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?

    Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations? by Ebru Yilmaz-Keskin, Ertan Sal, Luigia De Falco, Mariasole Bruno, Achille Iolascon, Ulker Koçak, Idil Yenicesu

    Published 2013-10-01
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  4. 4
    An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment

    An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment by Çiğdem Seher Kasapkara, Ebru Yılmaz-Keskin, Ferda Özbay-Hoşnut, Meltem Akçaboy, Emine Polat, Asburçe Olgaç, Pelin Zorlu

    Published 2019-04-01
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