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Showing results (411-420 of 431) with videos related to

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Leukemia|October 4, 2024
Monitoring clonal burden as an alternative to blast count for myelodysplastic neoplasm treatment responseMeagan A Jacoby, Eric D Duncavage, Ajay Khanna, et al.
The New England Journal of Medicine|March 11, 2021
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid CancersEric J Duncavage, Molly C Schroeder, Michele O'Laughlin, et al.
The New England Journal of Medicine|September 13, 2018
Mutation Clearance after Transplantation for Myelodysplastic SyndromeEric J Duncavage, Meagan A Jacoby, Gue Su Chang, et al.
American Journal of Medical Genetics. Part A|January 28, 2017
Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of HypophosphatasiaJair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
AIDS Research and Human Retroviruses|April 20, 2000
Effect of highly active antiretroviral therapy and thymic transplantation on immunoreconstitution in HIV infectionM L Markert, C B Hicks, J A Bartlett, et al.
Environmental Management|April 28, 2026
Assessing Potential Data Sources for Landscape-scale Terrestrial Biodiversity IndicatorsTom Bradfer-Lawrence, Meriel Harrison, Adham Ashton-Butt, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2021
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypesFrancesca Ferraro, Christopher A Miller, Keegan A Christensen, et al.
European Journal of Endocrinology|January 16, 2026
International guideline on genetic testing of children with short statureAndrew Dauber, Alexander A L Jorge, Ola Nilsson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2016
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan MutationsAlexandra Gkourogianni, Melissa Andrew, Leah Tyzinski, et al.
Human Mutation|September 9, 2014
A new overgrowth syndrome is due to mutations in RNF125Jair Tenorio, Alicia Mansilla, María Valencia, et al.
Pageof 44

Showing results (411-420 of 431) with videos related to

Sort By:
Pageof 44
Leukemia|October 4, 2024
Monitoring clonal burden as an alternative to blast count for myelodysplastic neoplasm treatment responseMeagan A Jacoby, Eric D Duncavage, Ajay Khanna, et al.
The New England Journal of Medicine|March 11, 2021
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid CancersEric J Duncavage, Molly C Schroeder, Michele O'Laughlin, et al.
The New England Journal of Medicine|September 13, 2018
Mutation Clearance after Transplantation for Myelodysplastic SyndromeEric J Duncavage, Meagan A Jacoby, Gue Su Chang, et al.
American Journal of Medical Genetics. Part A|January 28, 2017
Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of HypophosphatasiaJair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
AIDS Research and Human Retroviruses|April 20, 2000
Effect of highly active antiretroviral therapy and thymic transplantation on immunoreconstitution in HIV infectionM L Markert, C B Hicks, J A Bartlett, et al.
Environmental Management|April 28, 2026
Assessing Potential Data Sources for Landscape-scale Terrestrial Biodiversity IndicatorsTom Bradfer-Lawrence, Meriel Harrison, Adham Ashton-Butt, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2021
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypesFrancesca Ferraro, Christopher A Miller, Keegan A Christensen, et al.
European Journal of Endocrinology|January 16, 2026
International guideline on genetic testing of children with short statureAndrew Dauber, Alexander A L Jorge, Ola Nilsson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2016
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan MutationsAlexandra Gkourogianni, Melissa Andrew, Leah Tyzinski, et al.
Human Mutation|September 9, 2014
A new overgrowth syndrome is due to mutations in RNF125Jair Tenorio, Alicia Mansilla, María Valencia, et al.
Pageof 44