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H Steinberg

Showing results (751-760 of 766) with videos related to

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Circulation. Cardiovascular Interventions|October 6, 2011
Detection of lipid-core plaques by intracoronary near-infrared spectroscopy identifies high risk of periprocedural myocardial infarctionJames A Goldstein, Brijeshwar Maini, Simon R Dixon, et al.
Blood Cells, Molecules & Diseases|February 24, 2015
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemiaP Sebastiani, J J Farrell, A Alsultan, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
JAMA|April 4, 2003
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatmentMartin H Steinberg, Franca Barton, Oswaldo Castro, et al.
American Journal of Hematology|February 13, 2008
Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong KongGeoffrey T Gibney, Carolien I M Panhuysen, Jason C C So, et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2014
An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell diseaseElizabeth S Klings, Roberto F Machado, Robyn J Barst, et al.
The Journal of Clinical Investigation|September 22, 2012
The ADP receptor P2RY12 regulates osteoclast function and pathologic bone remodelingXinming Su, Desiree H Floyd, Alun Hughes, et al.
Plos One|May 5, 2012
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemiaJacqueline N Milton, Paola Sebastiani, Nadia Solovieff, et al.
The New England Journal of Medicine|December 7, 2020
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-ThalassemiaHaydar Frangoul, David Altshuler, M Domenica Cappellini, et al.
American Journal of Hematology|August 9, 2016
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemiaVinod Vathipadiekal, John J Farrell, Shuai Wang, et al.
Pageof 77

Showing results (751-760 of 766) with videos related to

Sort By:
Pageof 77
Circulation. Cardiovascular Interventions|October 6, 2011
Detection of lipid-core plaques by intracoronary near-infrared spectroscopy identifies high risk of periprocedural myocardial infarctionJames A Goldstein, Brijeshwar Maini, Simon R Dixon, et al.
Blood Cells, Molecules & Diseases|February 24, 2015
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemiaP Sebastiani, J J Farrell, A Alsultan, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
JAMA|April 4, 2003
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatmentMartin H Steinberg, Franca Barton, Oswaldo Castro, et al.
American Journal of Hematology|February 13, 2008
Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong KongGeoffrey T Gibney, Carolien I M Panhuysen, Jason C C So, et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2014
An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell diseaseElizabeth S Klings, Roberto F Machado, Robyn J Barst, et al.
The Journal of Clinical Investigation|September 22, 2012
The ADP receptor P2RY12 regulates osteoclast function and pathologic bone remodelingXinming Su, Desiree H Floyd, Alun Hughes, et al.
Plos One|May 5, 2012
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemiaJacqueline N Milton, Paola Sebastiani, Nadia Solovieff, et al.
The New England Journal of Medicine|December 7, 2020
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-ThalassemiaHaydar Frangoul, David Altshuler, M Domenica Cappellini, et al.
American Journal of Hematology|August 9, 2016
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemiaVinod Vathipadiekal, John J Farrell, Shuai Wang, et al.
Pageof 77