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Jan Inge Henter

Showing results (81-90 of 201) with videos related to

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Blood|January 18, 2003
Retraction. Neutrophil elastase mutations in severe congenital neutropenia patients of the original Kostmann familyAndrew A Aprikyan, Goran Carlsson, Steve Stein, et al.
British Journal of Haematology|October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) genePeter Gustavsson, Joakim Klar, Hans Matsson, et al.
Microbiology and Immunology|March 2, 2012
Killer cell immunoglobulin-like receptor gene polymorphisms predispose susceptibility to Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in Chinese childrenQin Qiang, Xie Zhengde, Liu Chunyan, et al.
British Journal of Haematology|May 27, 2005
Subtyping of natural killer cell cytotoxicity deficiencies in haemophagocytic lymphohistocytosis provides therapeutic guidanceAnnaCarin Horne, Chengyun Zheng, Ingrid Lorenz, et al.
The Journal of Pediatrics|October 1, 2003
Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: A prospective Nordic study of an unselected cohortSteen Rosthøj, Iris Hedlund-Treutiger, Jukka Rajantie, et al.
International Journal of Oncology|February 9, 2006
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell linesMaria B Karpova, Jacqueline Schoumans, Elisabeth Blennow, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 16, 2008
Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapyAnna Lindblom, Mats Heyman, Igge Gustafsson, et al.
Scientific Reports|November 9, 2018
Altered Populations of Unconventional T Cell Lineages in Patients with Langerhans Cell HistiocytosisJenée Mitchell, Egle Kvedaraite, Tatiana von Bahr Greenwood, et al.
Cancer|February 14, 2019
Haploinsufficiency of UNC13D increases the risk of lymphomaAlexandra Löfstedt, Clas Ahlm, Bianca Tesi, et al.
Molecular Medicine (Cambridge, Mass.)|December 31, 2020
Retraction Note to: High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndromeKarin Palmblad, Hanna Schierbeck, Erik Sundberg, et al.
Pageof 21

Showing results (81-90 of 201) with videos related to

Sort By:
Pageof 21
Blood|January 18, 2003
Retraction. Neutrophil elastase mutations in severe congenital neutropenia patients of the original Kostmann familyAndrew A Aprikyan, Goran Carlsson, Steve Stein, et al.
British Journal of Haematology|October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) genePeter Gustavsson, Joakim Klar, Hans Matsson, et al.
Microbiology and Immunology|March 2, 2012
Killer cell immunoglobulin-like receptor gene polymorphisms predispose susceptibility to Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in Chinese childrenQin Qiang, Xie Zhengde, Liu Chunyan, et al.
British Journal of Haematology|May 27, 2005
Subtyping of natural killer cell cytotoxicity deficiencies in haemophagocytic lymphohistocytosis provides therapeutic guidanceAnnaCarin Horne, Chengyun Zheng, Ingrid Lorenz, et al.
The Journal of Pediatrics|October 1, 2003
Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: A prospective Nordic study of an unselected cohortSteen Rosthøj, Iris Hedlund-Treutiger, Jukka Rajantie, et al.
International Journal of Oncology|February 9, 2006
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell linesMaria B Karpova, Jacqueline Schoumans, Elisabeth Blennow, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 16, 2008
Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapyAnna Lindblom, Mats Heyman, Igge Gustafsson, et al.
Scientific Reports|November 9, 2018
Altered Populations of Unconventional T Cell Lineages in Patients with Langerhans Cell HistiocytosisJenée Mitchell, Egle Kvedaraite, Tatiana von Bahr Greenwood, et al.
Cancer|February 14, 2019
Haploinsufficiency of UNC13D increases the risk of lymphomaAlexandra Löfstedt, Clas Ahlm, Bianca Tesi, et al.
Molecular Medicine (Cambridge, Mass.)|December 31, 2020
Retraction Note to: High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndromeKarin Palmblad, Hanna Schierbeck, Erik Sundberg, et al.
Pageof 21