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Jan Inge Henter

Showing results (141-150 of 201) with videos related to

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The Journal of Pediatrics|June 19, 2021
Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell HistiocytosisMilen Minkov, Ulrike Pötschger, Nirav Thacker, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 24, 2012
The need for worldwide policy and action plans for rare diseasesJohn Forman, Domenica Taruscio, Virginia A Llera, et al.
Pediatric Blood & Cancer|December 3, 2009
Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutationsMarie Meeths, Yenan T Bryceson, Eva Rudd, et al.
Journal of Medical Genetics|January 21, 2011
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3Elena Sieni, Valentina Cetica, Alessandra Santoro, et al.
Blood|April 17, 2013
Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosisHelmut Gadner, Milen Minkov, Nicole Grois, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Nature Medicine|December 25, 2007
Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusionFabienne Coury, Nicola Annels, Aymeric Rivollier, et al.
British Journal of Haematology|August 26, 2021
Response to mitogen-activated protein kinase inhibition of neurodegeneration in Langerhans cell histiocytosis monitored by cerebrospinal fluid neurofilament light as a biomarker: a pilot studyJan-Inge Henter, Egle Kvedaraite, Daniel Martín Muñoz, et al.
Blood Advances|August 12, 2020
Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 studyElisabet Bergsten, AnnaCarin Horne, Ida Hed Myrberg, et al.
British Journal of Haematology|December 19, 2014
Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhoodMaurizio Aricò, Itziar Astigarraga, Jorge Braier, et al.
Pageof 21

Showing results (141-150 of 201) with videos related to

Sort By:
Pageof 21
The Journal of Pediatrics|June 19, 2021
Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell HistiocytosisMilen Minkov, Ulrike Pötschger, Nirav Thacker, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 24, 2012
The need for worldwide policy and action plans for rare diseasesJohn Forman, Domenica Taruscio, Virginia A Llera, et al.
Pediatric Blood & Cancer|December 3, 2009
Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutationsMarie Meeths, Yenan T Bryceson, Eva Rudd, et al.
Journal of Medical Genetics|January 21, 2011
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3Elena Sieni, Valentina Cetica, Alessandra Santoro, et al.
Blood|April 17, 2013
Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosisHelmut Gadner, Milen Minkov, Nicole Grois, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Nature Medicine|December 25, 2007
Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusionFabienne Coury, Nicola Annels, Aymeric Rivollier, et al.
British Journal of Haematology|August 26, 2021
Response to mitogen-activated protein kinase inhibition of neurodegeneration in Langerhans cell histiocytosis monitored by cerebrospinal fluid neurofilament light as a biomarker: a pilot studyJan-Inge Henter, Egle Kvedaraite, Daniel Martín Muñoz, et al.
Blood Advances|August 12, 2020
Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 studyElisabet Bergsten, AnnaCarin Horne, Ida Hed Myrberg, et al.
British Journal of Haematology|December 19, 2014
Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhoodMaurizio Aricò, Itziar Astigarraga, Jorge Braier, et al.
Pageof 21