Rezultati pretrage - Christian Dohna‐Schwake

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  1. 1
    Targeted Therapy with Eculizumab for Inherited CD59 Deficiency

    Targeted Therapy with Eculizumab for Inherited CD59 Deficiency od Britta Höchsmann, Christian Dohna‐Schwake, Henriette Kyrieleis, Ulrich Pannicke, Hubert Schrezenmeier

    Izdano 2014
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  2. 2
    Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism

    Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism od A. K. Arbeiter, Birgitta Kranz, Anne‐Margret Wingen, Klaus-Eugen Bonzel, Christian Dohna‐Schwake, L. Hanssler, Ulrich Neudorf, Peter F. Hoyer, Rainer Büscher

    Izdano 2009
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  3. 3
    PICU mortality of children with cancer admitted to pediatric intensive care unit a systematic review and meta-analysis

    PICU mortality of children with cancer admitted to pediatric intensive care unit a systematic review and meta-analysis od Roelie M. Wösten–van Asperen, Josephus P. J. van Gestel, Martine van Grotel, Eva Tschiedel, Christian Dohna‐Schwake, Frédéric V. Valla, Jef Willems, Jeppe Sylvest Angaard Nielsen, Martín Krause, Jenny Potratz, Marry M. van den Heuvel‐Eibrink, Joe Brierley

    Izdano 2019
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  4. 4
    The Phoenix Sepsis Score in Pediatric Oncology Patients With Sepsis at PICU Admission: Test of Performance in a European Multicenter Cohort, 2018–2020

    The Phoenix Sepsis Score in Pediatric Oncology Patients With Sepsis at PICU Admission: Test of Performance in a European Multicenter Cohort, 2018–2020 od Roelie M. Wösten–van Asperen, Hannah M la Roi-Teeuw, Wim J. E. Tissing, Iolanda Jordán, Christian Dohna‐Schwake, Gabriella Bottari, John Pappachan, Roman Crazzolara, Angela Amigoni, Agnieszka Mizia‐Malarz, Andrea Moscatelli, María Sánchez‐Martín, Jef Willems, Luregn J. Schlapbach

    Izdano 2025
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  5. 5
    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2 od Derek Neilson, Mark D. Adams, Caitlin M.D. Orr, Deborah K. Schelling, Robert M. Eiben, Douglas S. Kerr, Jane Anderson, Alexander G. Bassuk, Ann Bye, Anne-Marie Childs, Antonia Clarke, Yanick J. Crow, Maja Di Rocco, Christian Dohna‐Schwake, Gregor Dueckers, Alfonso Fasano, Artemis Gika, Dimitris Gionnis, Mark Gorman, Padraic J. Grattan‐Smith, Annette Hackenberg, Alice Kuster, Markus Lentschig, Eduardo López‐Laso, Elysa J. Marco, Sotiria Mastroyianni, Julie Perrier, Thomas Schmitt‐Mechelke, Serenella Servidei, Angeliki Skardoutsou, Peter Uldall, Marjo S. van der Knaap, Karrie Goglin, David L. Tefft, Cristin Aubin, Philip L. De Jager, David A. Hafler, Matthew L. Warman

    Izdano 2009
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