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Jan Inge Henter

Showing results (171-180 of 201) with videos related to

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Blood|April 18, 2019
Recommendations for the management of hemophagocytic lymphohistiocytosis in adultsPaul La Rosée, AnnaCarin Horne, Melissa Hines, et al.
Blood|July 24, 2024
Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisitedJan-Inge Henter, Elena Sieni, Julia Eriksson, et al.
The Lancet. Oncology|April 3, 2025
Non-ICANS neurological complications after CAR T-cell therapies: recommendations from the EBMT Practice Harmonisation and Guidelines CommitteeCharlotte E Graham, Roser Velasco, Ana Alarcon Tomas, et al.
Plos One|December 29, 2023
Anakinra or tocilizumab in patients admitted to hospital with severe covid-19 at high risk of deterioration (IMMCoVA): A randomized, controlled, open-label trialJonas Sundén-Cullberg, Puran Chen, Henrike Häbel, et al.
Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
Journal of Internal Medicine|August 8, 2022
Targeting SAMHD1 with hydroxyurea in first-line cytarabine-based therapy of newly diagnosed acute myeloid leukaemia: Results from the HEAT-AML trialMartin Jädersten, Ingrid Lilienthal, Nikolaos Tsesmetzis, et al.
Cell Reports. Medicine|May 9, 2023
The single-cell transcriptional landscape of innate and adaptive lymphocytes in pediatric-onset colitisEfthymia Kokkinou, Tea Soini, Ram Vinay Pandey, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
Pageof 21

Showing results (171-180 of 201) with videos related to

Sort By:
Pageof 21
Blood|April 18, 2019
Recommendations for the management of hemophagocytic lymphohistiocytosis in adultsPaul La Rosée, AnnaCarin Horne, Melissa Hines, et al.
Blood|July 24, 2024
Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisitedJan-Inge Henter, Elena Sieni, Julia Eriksson, et al.
The Lancet. Oncology|April 3, 2025
Non-ICANS neurological complications after CAR T-cell therapies: recommendations from the EBMT Practice Harmonisation and Guidelines CommitteeCharlotte E Graham, Roser Velasco, Ana Alarcon Tomas, et al.
Plos One|December 29, 2023
Anakinra or tocilizumab in patients admitted to hospital with severe covid-19 at high risk of deterioration (IMMCoVA): A randomized, controlled, open-label trialJonas Sundén-Cullberg, Puran Chen, Henrike Häbel, et al.
Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
Journal of Internal Medicine|August 8, 2022
Targeting SAMHD1 with hydroxyurea in first-line cytarabine-based therapy of newly diagnosed acute myeloid leukaemia: Results from the HEAT-AML trialMartin Jädersten, Ingrid Lilienthal, Nikolaos Tsesmetzis, et al.
Cell Reports. Medicine|May 9, 2023
The single-cell transcriptional landscape of innate and adaptive lymphocytes in pediatric-onset colitisEfthymia Kokkinou, Tea Soini, Ram Vinay Pandey, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
Pageof 21