Bilaketaren emaitzak - Eva Al-Taji

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  1. 1
    Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism

    Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in domina... nork Eva Al Taji, Heike Biebermann, Z Límanová, O Hníková, Jaroslav Zikmund, Christof Dame, Annette Grüters, Jan Lebl, Heiko Krude

    Argitaratua 2007
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  2. 2
    Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome

    Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome nork Hans Christian Hennies, Anita Rauch, Wenke Seifert, Christian Schumi, Elisabeth Moser, Eva Al-Taji, Gholamali Tariverdian, Krystyńa Chrzańowska, Małgorzata Krajewska‐Walasek, Anna Rajab, Roberto Giugliani, Thomas Neumann, Katja‐Martina Eckl, Mohsen Karbasiyan, André Reis, Denise Horn

    Argitaratua 2004
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  3. 3
    Effect of Hydrolyzed Infant Formula vs Conventional Formula on Risk of Type 1 Diabetes

    Effect of Hydrolyzed Infant Formula vs Conventional Formula on Risk of Type 1 Diabetes nork Mikael Knip, Hans K. Åkerblom, Eva Al Taji, Dorothy Becker, Jan Bruining, Luís Castaño, Thomas Danne, Carine de Beaufort, Hans‐Michael Dosch, John Dupré, William D. Fraser, Neville J. Howard, Jorma Ilonen, Daniel Konrad, Olga Kordonouri, Jeffrey P. Krischer, Margaret L. Lawson, Johnny Ludvigsson, L Madácsy, Jeffrey L. Mahon, Anne Ormisson, Jerry P. Palmer, Paolo Pozzilli, Erkki Savilahti, Manuel Serrano‐Ríos, Marco Songini, Shayne Taback, Outi Vaarala, Neil H. White, Suvi Μ. Virtanen, R Wasikówa

    Argitaratua 2018
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