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Holger Cario

Showing results (21-30 of 60) with videos related to

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British Journal of Haematology|February 19, 2014
Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimerasMor Gross, Nathalie Ben-Califa, Mary F McMullin, et al.
Journal of Personalized Medicine|July 27, 2022
Transition in Sickle Cell Disease (SCD): A German Consensus RecommendationFerras Alashkar, Carmen Aramayo-Singelmann, Janine Böll, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|December 11, 2023
Segmental quantification of hepatic lipid content based on volumetric MRI data in patients with suspected iron overloadArthur P Wunderlich, Holger Cario, Stephan Kannengießer, et al.
Pediatric Blood & Cancer|June 19, 2013
Erythrocytosis in children and adolescents-classification, characterization, and consensus recommendations for the diagnostic approachHolger Cario, Mary Frances McMullin, Celeste Bento, et al.
Haematologica|January 12, 2005
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosisHolger Cario, Klaus Schwarz, Norbert Jorch, et al.
European Journal of Haematology|September 7, 2018
Serum ferritin is not a reliable predictor to determine iron overload in thalassemia major patients post-hematopoietic stem cell transplantationAndrea Jarisch, Emilia Salzmann-Manrique, Holger Cario, et al.
European Radiology Experimental|February 1, 2019
Quantitative DWI predicts event-free survival in children with neuroblastic tumours: preliminary findings from a retrospective cohort studyAnna-Lydia Peschmann, Meinrad Beer, Bettina Ammann, et al.
Pediatric Blood & Cancer|March 5, 2025
A Toolkit for Healthcare Transition for Adolescents With Classical Myeloproliferative NeoplasmsNicole Kucine, Holger Cario, Ghaith Abu-Zeinah, et al.
Haematologica|May 10, 2007
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosisSusana Rives, Heike L Pahl, Lourdes Florensa, et al.
British Journal of Haematology|October 8, 2024
Shwachman-Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancyHolger Cario, Alexis Bertrand, Shengjiang Tan, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|February 19, 2014
Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimerasMor Gross, Nathalie Ben-Califa, Mary F McMullin, et al.
Journal of Personalized Medicine|July 27, 2022
Transition in Sickle Cell Disease (SCD): A German Consensus RecommendationFerras Alashkar, Carmen Aramayo-Singelmann, Janine Böll, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|December 11, 2023
Segmental quantification of hepatic lipid content based on volumetric MRI data in patients with suspected iron overloadArthur P Wunderlich, Holger Cario, Stephan Kannengießer, et al.
Pediatric Blood & Cancer|June 19, 2013
Erythrocytosis in children and adolescents-classification, characterization, and consensus recommendations for the diagnostic approachHolger Cario, Mary Frances McMullin, Celeste Bento, et al.
Haematologica|January 12, 2005
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosisHolger Cario, Klaus Schwarz, Norbert Jorch, et al.
European Journal of Haematology|September 7, 2018
Serum ferritin is not a reliable predictor to determine iron overload in thalassemia major patients post-hematopoietic stem cell transplantationAndrea Jarisch, Emilia Salzmann-Manrique, Holger Cario, et al.
European Radiology Experimental|February 1, 2019
Quantitative DWI predicts event-free survival in children with neuroblastic tumours: preliminary findings from a retrospective cohort studyAnna-Lydia Peschmann, Meinrad Beer, Bettina Ammann, et al.
Pediatric Blood & Cancer|March 5, 2025
A Toolkit for Healthcare Transition for Adolescents With Classical Myeloproliferative NeoplasmsNicole Kucine, Holger Cario, Ghaith Abu-Zeinah, et al.
Haematologica|May 10, 2007
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosisSusana Rives, Heike L Pahl, Lourdes Florensa, et al.
British Journal of Haematology|October 8, 2024
Shwachman-Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancyHolger Cario, Alexis Bertrand, Shengjiang Tan, et al.
Pageof 6