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Holger Cario

Showing results (51-60 of 60) with videos related to

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Clinical Chemistry and Laboratory Medicine|February 10, 2021
High-resolution pediatric reference intervals for 15 biochemical analytes described using fractional polynomialsJakob Zierk, Hannsjörg Baum, Alexander Bertram, et al.
Clinical Chemistry and Laboratory Medicine|April 22, 2019
Next-generation reference intervals for pediatric hematologyJakob Zierk, Johannes Hirschmann, Dennis Toddenroth, et al.
European Journal of Haematology|November 22, 2007
Relative response of patients with myelodysplastic syndromes and other transfusion-dependent anaemias to deferasirox (ICL670): a 1-yr prospective studyJohn Porter, Renzo Galanello, Giuseppe Saglio, et al.
Pediatric Blood & Cancer|December 24, 2019
Sickle cell disease in Germany: Results from a national registryJoachim B Kunz, Stephan Lobitz, Regine Grosse, et al.
Blood|June 13, 2018
Identification of a new <i>VHL</i> exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau diseaseMarion Lenglet, Florence Robriquet, Klaus Schwarz, et al.
Human Mutation|October 12, 2013
Genetic basis of congenital erythrocytosis: mutation update and online databasesCeleste Bento, Melanie J Percy, Betty Gardie, et al.
The New England Journal of Medicine|April 30, 2025
Identification of Hepatic-like EPO as a Cause of PolycythemiaLaurent Martin, Darko Maric, Salam Idriss, et al.
European Journal of Cancer (Oxford, England : 1990)|October 2, 2018
PanCareLIFE: The scientific basis for a European project to improve long-term care regarding fertility, ototoxicity and health-related quality of life after cancer occurring among children and adolescentsJulianne Byrne, Desiree Grabow, Helen Campbell, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Nature Genetics|May 19, 2015
Factors influencing success of clinical genome sequencing across a broad spectrum of disordersJenny C Taylor, Hilary C Martin, Stefano Lise, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Clinical Chemistry and Laboratory Medicine|February 10, 2021
High-resolution pediatric reference intervals for 15 biochemical analytes described using fractional polynomialsJakob Zierk, Hannsjörg Baum, Alexander Bertram, et al.
Clinical Chemistry and Laboratory Medicine|April 22, 2019
Next-generation reference intervals for pediatric hematologyJakob Zierk, Johannes Hirschmann, Dennis Toddenroth, et al.
European Journal of Haematology|November 22, 2007
Relative response of patients with myelodysplastic syndromes and other transfusion-dependent anaemias to deferasirox (ICL670): a 1-yr prospective studyJohn Porter, Renzo Galanello, Giuseppe Saglio, et al.
Pediatric Blood & Cancer|December 24, 2019
Sickle cell disease in Germany: Results from a national registryJoachim B Kunz, Stephan Lobitz, Regine Grosse, et al.
Blood|June 13, 2018
Identification of a new <i>VHL</i> exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau diseaseMarion Lenglet, Florence Robriquet, Klaus Schwarz, et al.
Human Mutation|October 12, 2013
Genetic basis of congenital erythrocytosis: mutation update and online databasesCeleste Bento, Melanie J Percy, Betty Gardie, et al.
The New England Journal of Medicine|April 30, 2025
Identification of Hepatic-like EPO as a Cause of PolycythemiaLaurent Martin, Darko Maric, Salam Idriss, et al.
European Journal of Cancer (Oxford, England : 1990)|October 2, 2018
PanCareLIFE: The scientific basis for a European project to improve long-term care regarding fertility, ototoxicity and health-related quality of life after cancer occurring among children and adolescentsJulianne Byrne, Desiree Grabow, Helen Campbell, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Nature Genetics|May 19, 2015
Factors influencing success of clinical genome sequencing across a broad spectrum of disordersJenny C Taylor, Hilary C Martin, Stefano Lise, et al.
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