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Stephan Ehl

Showing results (81-90 of 239) with videos related to

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Clinical Immunology (Orlando, Fla.)|June 14, 2011
Clinical and immunological manifestations of patients with atypical severe combined immunodeficiencyKerstin Felgentreff, Ruy Perez-Becker, Carsten Speckmann, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 13, 2015
T cell expansion is the limiting factor of virus control in mice with attenuated TCR signaling: implications for human immunodeficiencyKristina M Hillen, Ruth Gather, Anselm Enders, et al.
Cells|February 15, 2022
Dysregulated PI3K Signaling in B Cells of CVID PatientsIna Harder, Matthias Münchhalfen, Geoffroy Andrieux, et al.
Frontiers in Oncology|December 28, 2020
Altered T-Lymphocyte Biology Following High-Dose Melphalan and Autologous Stem Cell Transplantation With Implications for Adoptive T-Cell TherapyThomas Mika, Swetlana Ladigan-Badura, Abdelouahid Maghnouj, et al.
Blood Advances|October 7, 2022
MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicityKerstin Schütze, Miriam Groß, Kerstin Cornils, et al.
EMBO Molecular Medicine|July 3, 2013
Disease-causing mutations in the XIAP BIR2 domain impair NOD2-dependent immune signallingRune Busk Damgaard, Berthe Katrine Fiil, Carsten Speckmann, et al.
JMIR Medical Informatics|October 7, 2020
Enabling External Inquiries to an Existing Patient Registry by Using the Open Source Registry System for Rare Diseases: Demonstration of the System Using the European Society for Immunodeficiencies RegistryRaphael Scheible, Dennis Kadioglu, Stephan Ehl, et al.
Scandinavian Journal of Immunology|August 6, 2019
Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase-No detection by newborn screening for primary immunodeficienciesRenate Krüger, Ulrich Baumann, Stephan Borte, et al.
Pediatric Blood & Cancer|December 16, 2014
Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorptionMiriam Erlacher, Sarah Catharina Grünert, Annamaria Cseh, et al.
Journal of Clinical Immunology|December 11, 2014
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with HypogammaglobulinemiaHossein Esmaeilzadeh, Mohammad Hasan Bemanian, Mohammad Nabavi, et al.
Pageof 24

Showing results (81-90 of 239) with videos related to

Sort By:
Pageof 24
Clinical Immunology (Orlando, Fla.)|June 14, 2011
Clinical and immunological manifestations of patients with atypical severe combined immunodeficiencyKerstin Felgentreff, Ruy Perez-Becker, Carsten Speckmann, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 13, 2015
T cell expansion is the limiting factor of virus control in mice with attenuated TCR signaling: implications for human immunodeficiencyKristina M Hillen, Ruth Gather, Anselm Enders, et al.
Cells|February 15, 2022
Dysregulated PI3K Signaling in B Cells of CVID PatientsIna Harder, Matthias Münchhalfen, Geoffroy Andrieux, et al.
Frontiers in Oncology|December 28, 2020
Altered T-Lymphocyte Biology Following High-Dose Melphalan and Autologous Stem Cell Transplantation With Implications for Adoptive T-Cell TherapyThomas Mika, Swetlana Ladigan-Badura, Abdelouahid Maghnouj, et al.
Blood Advances|October 7, 2022
MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicityKerstin Schütze, Miriam Groß, Kerstin Cornils, et al.
EMBO Molecular Medicine|July 3, 2013
Disease-causing mutations in the XIAP BIR2 domain impair NOD2-dependent immune signallingRune Busk Damgaard, Berthe Katrine Fiil, Carsten Speckmann, et al.
JMIR Medical Informatics|October 7, 2020
Enabling External Inquiries to an Existing Patient Registry by Using the Open Source Registry System for Rare Diseases: Demonstration of the System Using the European Society for Immunodeficiencies RegistryRaphael Scheible, Dennis Kadioglu, Stephan Ehl, et al.
Scandinavian Journal of Immunology|August 6, 2019
Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase-No detection by newborn screening for primary immunodeficienciesRenate Krüger, Ulrich Baumann, Stephan Borte, et al.
Pediatric Blood & Cancer|December 16, 2014
Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorptionMiriam Erlacher, Sarah Catharina Grünert, Annamaria Cseh, et al.
Journal of Clinical Immunology|December 11, 2014
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with HypogammaglobulinemiaHossein Esmaeilzadeh, Mohammad Hasan Bemanian, Mohammad Nabavi, et al.
Pageof 24