Resultados de procura - Jan‐Inge Henter

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  1. 1
    Fatal agranulocytosis after deferiprone therapy in a child with Diamond-Blackfan anemia

    Fatal agranulocytosis after deferiprone therapy in a child with Diamond-Blackfan anemia por Jan‐Inge Henter, Jonas Karlén

    Publicado 2007
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  2. 2
    Malignancy-associated hemophagocytic lymphohistiocytosis in Sweden: incidence, clinical characteristics, and survival

    Malignancy-associated hemophagocytic lymphohistiocytosis in Sweden: incidence, clinical characteristics, and survival por Alexandra Löfstedt, Martin Jädersten, Marie Meeths, Jan‐Inge Henter

    Publicado 2023
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  3. 3
    Talking about Death with Children Who Have Severe Malignant Disease

    Talking about Death with Children Who Have Severe Malignant Disease por Ulrika Kreicbergs, Unnur Valdimarsdóttir, Erik Onelöv, Jan‐Inge Henter, Gunnar Steineck

    Publicado 2004
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  4. 4
    On the Child's Own Initiative: Parents Communicate with Their Dying Child About Death

    On the Child's Own Initiative: Parents Communicate with Their Dying Child About Death por Li Jalmsell, Taru Kontio, Maria Stein, Jan‐Inge Henter, Ulrika Kreicbergs

    Publicado 2014
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  5. 5
    Hypercytokinemia in familial hemophagocytic lymphohistiocytosis

    Hypercytokinemia in familial hemophagocytic lymphohistiocytosis por Jan‐Inge Henter, Göran Elinder, Olle Söder, Magnus Hansson, Birger Andersson, Jan Andersson

    Publicado 1991
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  6. 6
    Care-Related Distress: A Nationwide Study of Parents Who Lost Their Child to Cancer

    Care-Related Distress: A Nationwide Study of Parents Who Lost Their Child to Cancer por Ulrika Kreicbergs, Unnur Valdimarsdóttir, Erik Onelöv, Olle Björk, Gunnar Steineck, Jan‐Inge Henter

    Publicado 2005
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  7. 7
    Frequency and development of CNS involvement in Chinese children with hemophagocytic lymphohistiocytosis

    Frequency and development of CNS involvement in Chinese children with hemophagocytic lymphohistiocytosis por Shuang Yang, Li Zhang, Chenguang Jia, Honghao Ma, Jan‐Inge Henter, Kunling Shen

    Publicado 2009
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  8. 8
    Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia

    Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia por Göran Carlsson, Anders Fasth, Elisabet Berglöf, Kristina Lagerstedt‐Robinson, Magnus Nordenskjöld, Jan Palmblad, Jan‐Inge Henter, Bengt Fadeel

    Publicado 2012
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  9. 9
    How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis?

    How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis? por AnnaCarin Horne, Ronny Wickström, Michael B. Jordan, E. Ann Yeh, Ahmed Naqvi, Jan‐Inge Henter, Gritta Janka

    Publicado 2017
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  10. 10
    Parvovirus B19 Infection in Children with Acute Lymphoblastic Leukemia is Associated with Cytopenia Resulting in Prolonged Interruptions of Chemotherapy

    Parvovirus B19 Infection in Children with Acute Lymphoblastic Leukemia is Associated with Cytopenia Resulting in Prolonged Interruptions of Chemotherapy por Anna Lindblom, Mats Heyman, Finn Gustafsson, Oscar Norbeck, Tove Kaldensjö, Åsa Vernby, Jan‐Inge Henter, Thomas Tolfvenstam, Kristina Broliden

    Publicado 2008
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  11. 11
    High Systemic Levels of the Cytokine-Inducing HMGB1 Isoform Secreted in Severe Macrophage Activation Syndrome

    High Systemic Levels of the Cytokine-Inducing HMGB1 Isoform Secreted in Severe Macrophage Activation Syndrome por Karin Palmblad, Hanna Schierbeck, Erik Sundberg, AnnaCarin Horne, Helena Erlandsson Harris, Jan‐Inge Henter, Daniel J. Antoine, Jan Andersson

    Publicado 2014
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  12. 12
    SAMHD1 protects cancer cells from various nucleoside-based antimetabolites

    SAMHD1 protects cancer cells from various nucleoside-based antimetabolites por Nikolas Herold, Sean G. Rudd, Kumar Sanjiv, Juliane Kutzner, Julia Bladh, Cynthia B. J. Paulin, Thomas Helleday, Jan‐Inge Henter, Torsten Schaller

    Publicado 2017
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  13. 13
    Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells

    Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myelo... por Göran Carlsson, Andrew A.G. Aprikyan, Ramin Tehranchi, David C. Dale, Anna Porwit, Eva Hellström-Lindberg, Jan Palmblad, Jan‐Inge Henter, Bengt Fadeel

    Publicado 2004
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  14. 14
    Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification

    Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification por Helmut Gadner, Nicole Grois, Ulrike Pötschger, Milen Minkov, Maurizio Aricò, Jorge Braier, Valerie Broadbent, Jean Donadieu, Jan‐Inge Henter, Robert McCarter, Stephan Ladisch

    Publicado 2007
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  15. 15
    Dengue Infection Complicated by Hemophagocytic Lymphohistiocytosis: Experiences From 180 Patients With Severe Dengue

    Dengue Infection Complicated by Hemophagocytic Lymphohistiocytosis: Experiences From 180 Patients With Severe Dengue por Foong Kee Kan, Cheng Cheng Tan, Tatiana von Bahr Greenwood, Khairil Erwan Khalid, Premaa Supramaniam, Ida Hed Myrberg, Lian Huat Tan, Jan‐Inge Henter

    Publicado 2019
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  16. 16
    Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol

    Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol por Helena Trottestam, AnnaCarin Horne, Maurizio Aricò, R. Maarten Egeler, Alexandra H. Filipovich, Helmut Gadner, Shinsaku Imashuku, Stephan Ladisch, David Webb, Gritta Janka, Jan‐Inge Henter

    Publicado 2011
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  17. 17
    Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

    Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11 por Udo zur Stadt, Susanne Schmidt, Brigitte Kasper, Karin Beutel, A. Sarper Diler, Jan‐Inge Henter, H. Kabisch, Reinhard Schneppenheim, Peter Nürnberg, Gritta Janka, Hans Christian Hennies

    Publicado 2005
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  18. 18
    With me or against me: Tumor suppressor and drug resistance activities of SAMHD1

    With me or against me: Tumor suppressor and drug resistance activities of SAMHD1 por Nikolas Herold, Sean G. Rudd, Kumar Sanjiv, Juliane Kutzner, Ida Hed Myrberg, Cynthia B. J. Paulin, Thale Kristin Olsen, Thomas Helleday, Jan‐Inge Henter, Torsten Schaller

    Publicado 2017
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  19. 19
    Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific <i>HAX1</i> mutations

    Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific <i>HAX1</i> mutations por Göran Carlsson, Ingrid van’t Hooft, Malin Melin, Miriam Entesarian, Evaldas Laurenčikas, Inger Nennesmo, Alicja Trębińska, Ewa A. Grzybowska, Jan Palmblad, Niklas Dahl, Magnus Nordenskjöld, Bengt Fadeel, Jan‐Inge Henter

    Publicado 2008
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  20. 20
    Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3

    Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3 por Elena Sieni, Valentina Cetica, Alessandra Santoro, K. Beutel, E. Mastrodicasa, Marie Meeths, Benedetta Ciambotti, Francesca Brugnolo, Udo zur Stadt, Daniela Pende, Lorenzo Moretta, Gillian M. Griffiths, Jan‐Inge Henter, Gritta Janka, Maurizio Aricò

    Publicado 2011
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