Resultados da pesquisa - Giridharan Appaswamy

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  1. 1
    The phenotype of human STK4 deficiency

    The phenotype of human STK4 deficiency Por Hengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, Jana Diestelhorst, Rita Beier, Alejandro A. Schäffer, E. Michael Gertz, Axel Schambach, Hans Kreipe, Dietmar Pfeifer, Karin R. Engelhardt, Nima Rezaei, Bodo Grimbacher, Sabine Lohrmann, Roya Sherkat, Christoph Klein

    Publicado em 2012
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  2. 2
    A Syndrome with Congenital Neutropenia and Mutations in<i>G6PC3</i>

    A Syndrome with Congenital Neutropenia and Mutations in<i>G6PC3</i> Por Kaan Boztuğ, Giridharan Appaswamy, Angel Ashikov, Alejandro A. Schäffer, Ulrich Salzer, Jana Diestelhorst, Manuela Germeshausen, Gudrun Brandes, Jacqueline Lee-Gossler, Fatih Noyan, Anna-Katherina Gatzke, Milen Minkov, Johann Greil, Christian P. Kratz, Theoni Petropoulou, Isabelle Pellier, Christine Bellanné‐Chantelot, Nima Rezaei, Kirsten Mönkemöller, Noha Irani-Hakimeh, Hans Bakker, Rita Gerardy‐Schahn, Cornelia Zeidler, Bodo Grimbacher, Karl Welte, Christoph Klein

    Publicado em 2008
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  3. 3
    JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia

    JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia Por Kaan Boztuğ, Päivi M. Järvinen, Elisabeth Salzer, Tomáš Raček, Sebastian Mönch, Wojciech Garncarz, E. Michael Gertz, Alejandro A. Schäffer, Aristotelis Antonopoulos, Stuart M. Haslam, Lena Schieck, Jacek Puchałka, Jana Diestelhorst, Giridharan Appaswamy, Brigitte Lescoeur, Roberto Giambruno, Johannes W. Bigenzahn, Ulrich Elling, Dietmar Pfeifer, Cecilia Domínguez Conde, Michael H. Albert, Karl Welte, Gudrun Brandes, Roya Sherkat, Jutte van der Werff ten Bosch, Nima Rezaei, Amos Etzioni, Christine Bellanné‐Chantelot, Giulio Superti‐Furga, Josef Penninger, Keiryn L. Bennett, Julia von Blume, Anne Dell, Jean Donadieu, Christoph Klein

    Publicado em 2014
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