Search Results - Göransdotter Ericson, Kim

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  1. 1
    Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

    Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis by Göransdotter Ericson, Kim, Fadeel, Bengt, Nilsson-Ardnor, Sofie, Söderhäll, Cilla, Samuelsson, AnnaCarin, Janka, Gritta, Schneider, Marion, Gürgey, Aytemiz, Yalman, Nevin, Révész, Tom, Egeler, R. Maarten, Jahnukainen, Kirsi, Storm-Mathiesen, Ingebjörg, Haraldsson, Ásgeir, Poole, Janet, de Saint Basile, Geneviève, Nordenskjöld, Magnus, Henter, Jan-Inge

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  2. 2
    Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original Kostmann family in northern Sweden

    Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original... by Carlsson, G, Aprikyan, AA, Ericson, KG, Stein, S, Makaryan, V, Dale, DC, Nordenskjold, M, Fadeel, B, Palmblad, J, Hentera, JI

    Published in Haematologica (Roma)
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  3. 3
    Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis

    Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis by ERICSON, Kim Göransdotter, FADEEL, Bengt, ANDERSSON, Mats, GUDMUNDSSON, Gudmundur H, GÜRGEY, Aytemiz, YALMAN, Nevin, JANKA, Gritta, NORDENSKJÖLD, Magnus, HENTER, Jan-Inge

    Published in Human genetics
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  4. 4
    Clinical and Genetic Studies of Familial Hemophagocytic Lymphohistiocytosis in Oman: Need for Early Treatment

    Clinical and Genetic Studies of Familial Hemophagocytic Lymphohistiocytosis in Oman: Need for Early Treatment by Al-Lamki, Zakia, Wali, Yasser A., Pathare, Anil, Ericson, Kim Göransdotter, Henter, Jan-Inge

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  5. 5
    Clinical and Genetic Studies of Familial Hemophagocytic Lymphohistiocytosis in Oman: Need for Early Treatment

    Clinical and Genetic Studies of Familial Hemophagocytic Lymphohistiocytosis in Oman: Need for Early Treatment by Al-Lamki, Zakia, Wali, Yasser, Pathare, Anil, Ericson, Kim Göransdotter, Henter, Jan-Inge

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  6. 6
    Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original Kostmann family in northern Sweden (vol 91, pg 589, 2006)

    Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original... by Carlsson, G, Aprikyan, AAG, Ericson, KG, Stein, S, Makaryan, V, Dale, DC, Nordenskjold, M, Fadeel, B, Palmblad, J, Henter, JI

    Published in Haematologica (Roma)
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