Hasil Pencarian - Emma Westermann-Clark

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  1. 1
    Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome

    Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome oleh Claudia L. Gaefke, Jonathan Metts, Donya Imanirad, Daime Nieves, Paola Terranova, Gianluca Dell'Orso, Eleonora Gambineri, Maurizio Miano, Richard F. Lockey, Jolan Eszter Walter, Jolan Eszter Walter, Emma Westermann-Clark, Emma Westermann-Clark

    Diterbitkan 2021-03-01
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  2. 2
    Primary Immunodeficiency in Children With Autoimmune Cytopenias: Retrospective 154-Patient Cohort

    Primary Immunodeficiency in Children With Autoimmune Cytopenias: Retrospective 154-Patient Cohort oleh Emma Westermann-Clark, Emma Westermann-Clark, Cristina Adelia Meehan, Anna K. Meyer, Anna K. Meyer, Joseph F. Dasso, Joseph F. Dasso, Devendra Amre, Maryssa Ellison, Bhumika Patel, Marisol Betensky, Marisol Betensky, Charles Isaac Hauk, Jennifer Mayer, Jonathan Metts, Jennifer W. Leiding, Jennifer W. Leiding, Panida Sriaroon, Panida Sriaroon, Ambuj Kumar, Irmel Ayala, Irmel Ayala, Jolan E. Walter, Jolan E. Walter, Jolan E. Walter

    Diterbitkan 2021-04-01
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  3. 3
    Matrix Metalloproteinase 7 Expression and Apical Epithelial Defects in <i>Atp8b1</i> Mutant Mouse Model of Pulmonary Fibrosis

    Matrix Metalloproteinase 7 Expression and Apical Epithelial Defects in <i>Atp8b1</i> Mutant Mouse Model of Pulmonary Fibrosis oleh Emma Westermann-Clark, Ramani Soundararajan, Jutaro Fukumoto, Sahebgowda Sidramagowda Patil, Timothy M. Stearns, Smita Saji, Alexander Czachor, Helena Hernandez-Cuervo, Mason Breitzig, Sudarshan Krishnamurthy, Richard F. Lockey, Narasaiah Kolliputi

    Diterbitkan 2022-02-01
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  4. 4
    Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma

    Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma oleh Maria Chitty-Lopez, Emma Westermann-Clark, Irina Dawson, Boglarka Ujhazi, Krisztian Csomos, Kerry Dobbs, Khuong Le, Yasuhiro Yamazaki, Amir A. Sadighi Akha, Deepak Chellapandian, Ben Oshrine, Luigi D. Notarangelo, Gauri Sunkersett, Jennifer W. Leiding, Jolan E. Walter, Jolan E. Walter

    Diterbitkan 2020-09-01
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  5. 5
    Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50

    Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 oleh Manfred Fliegauf, Manfred Fliegauf, Matias Kinnunen, Sara Posadas-Cantera, Nadezhda Camacho-Ordonez, Nadezhda Camacho-Ordonez, Hassan Abolhassani, Hassan Abolhassani, Laia Alsina, Laia Alsina, Faranaz Atschekzei, Faranaz Atschekzei, Delfien J. Bogaert, Delfien J. Bogaert, Siobhan O. Burns, Siobhan O. Burns, Joseph A. Church, Gregor Dückers, Alexandra F. Freeman, Lennart Hammarström, Leif Gunnar Hanitsch, Tessa Kerre, Robin Kobbe, Svetlana O. Sharapova, Kathrin Siepermann, Carsten Speckmann, Carsten Speckmann, Sophie Steiner, Nisha Verma, Jolan E. Walter, Jolan E. Walter, Jolan E. Walter, Emma Westermann-Clark, Emma Westermann-Clark, Sigune Goldacker, Sigune Goldacker, Klaus Warnatz, Klaus Warnatz, Markku Varjosalo, Markku Varjosalo, Markku Varjosalo, Bodo Grimbacher, Bodo Grimbacher, Bodo Grimbacher, Bodo Grimbacher

    Diterbitkan 2022-08-01
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