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Jan Inge Henter

Showing results (161-170 of 201) with videos related to

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Pediatric Blood & Cancer|January 7, 2024
The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosisVassilios Papadakis, Itziar Astigarraga, Cor van den Bos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 25, 2020
Patients with both Langerhans cell histiocytosis and Crohn's disease highlight a common role of interleukin-23Egle Kvedaraite, Magda Lourda, HongYa Han, et al.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, et al.
Blood|May 26, 2007
Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patientsYenan T Bryceson, Eva Rudd, Chengyun Zheng, et al.
Blood|June 19, 2010
Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2Marie Meeths, Miriam Entesarian, Waleed Al-Herz, et al.
Bone Marrow Transplantation|April 9, 2025
Less frequent complications following CAR T-cell therapies: hemophagocytic lymphohistiocytosis, graft-versus-host disease, thrombotic microangiopathy, coagulation disorders and secondary malignancies: best practice recommendations from the EBMT Practice Harmonization and Guidelines CommitteeGuillermo Ortí, Guillaume Dachy, Charlotte E Graham, et al.
Blood Cancer Journal|October 21, 2018
Low-level expression of SAMHD1 in acute myeloid leukemia (AML) blasts correlates with improved outcome upon consolidation chemotherapy with high-dose cytarabine-based regimensGeorge Z Rassidakis, Nikolas Herold, Ida Hed Myrberg, et al.
Critical Care Medicine|October 4, 2021
Consensus-Based Guidelines for the Recognition, Diagnosis, and Management of Hemophagocytic Lymphohistiocytosis in Critically Ill Children and AdultsMelissa R Hines, Tatiana von Bahr Greenwood, Gernot Beutel, et al.
The Journal of Allergy and Clinical Immunology|January 17, 2015
Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiencyBianca Tesi, Elena Sieni, Conceição Neves, et al.
Blood|February 2, 2012
A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromesYenan T Bryceson, Daniela Pende, Andrea Maul-Pavicic, et al.
Pageof 21

Showing results (161-170 of 201) with videos related to

Sort By:
Pageof 21
Pediatric Blood & Cancer|January 7, 2024
The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosisVassilios Papadakis, Itziar Astigarraga, Cor van den Bos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 25, 2020
Patients with both Langerhans cell histiocytosis and Crohn's disease highlight a common role of interleukin-23Egle Kvedaraite, Magda Lourda, HongYa Han, et al.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, et al.
Blood|May 26, 2007
Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patientsYenan T Bryceson, Eva Rudd, Chengyun Zheng, et al.
Blood|June 19, 2010
Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2Marie Meeths, Miriam Entesarian, Waleed Al-Herz, et al.
Bone Marrow Transplantation|April 9, 2025
Less frequent complications following CAR T-cell therapies: hemophagocytic lymphohistiocytosis, graft-versus-host disease, thrombotic microangiopathy, coagulation disorders and secondary malignancies: best practice recommendations from the EBMT Practice Harmonization and Guidelines CommitteeGuillermo Ortí, Guillaume Dachy, Charlotte E Graham, et al.
Blood Cancer Journal|October 21, 2018
Low-level expression of SAMHD1 in acute myeloid leukemia (AML) blasts correlates with improved outcome upon consolidation chemotherapy with high-dose cytarabine-based regimensGeorge Z Rassidakis, Nikolas Herold, Ida Hed Myrberg, et al.
Critical Care Medicine|October 4, 2021
Consensus-Based Guidelines for the Recognition, Diagnosis, and Management of Hemophagocytic Lymphohistiocytosis in Critically Ill Children and AdultsMelissa R Hines, Tatiana von Bahr Greenwood, Gernot Beutel, et al.
The Journal of Allergy and Clinical Immunology|January 17, 2015
Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiencyBianca Tesi, Elena Sieni, Conceição Neves, et al.
Blood|February 2, 2012
A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromesYenan T Bryceson, Daniela Pende, Andrea Maul-Pavicic, et al.
Pageof 21