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H Steinberg

Showing results (541-550 of 766) with videos related to

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The Journal of Clinical Investigation|December 1, 1991
Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitA K Gupta, K A Kirchner, R Nicholson, et al.
American Journal of Hematology|October 11, 2007
Sickle cell bone disease: response to vitamin D and calciumAdeboye H Adewoye, Tai C Chen, Qianli Ma, et al.
American Journal of Hematology|November 14, 2008
Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobinIbifiri Wilcox, Kevin Boettger, Lance Greene, et al.
The American Journal of Cardiology|August 1, 1996
Dobutamine stress testing in the cardiac catheterization laboratoryS P Sedlis, J Lorin, A Matalon, et al.
Psychoneuroendocrinology|January 1, 1990
Endogenous opioids modulate the cardiovascular response to mental stressM Morris, P Salmon, H Steinberg, et al.
American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|June 21, 2014
Initial experience with the novel patent foramen ovale occlusion device Nit-Occlud® in patients with stroke or transient ischemic attackDaniel H Steinberg, Stefan C Bertog, Julia Momberger, et al.
Blood|April 15, 2011
Fetal hemoglobin in sickle cell anemiaIdowu Akinsheye, Abdulrahman Alsultan, Nadia Solovieff, et al.
Proteomics|May 3, 2002
An improved formulation of SYPRO Ruby protein gel stain: comparison with the original formulation and with a ruthenium II tris (bathophenanthroline disulfonate) formulationKiera N Berggren, Birte Schulenberg, Mary F Lopez, et al.
The American Journal of the Medical Sciences|August 1, 1992
Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoterM B Coleman, J G Adams, M W Plonczynski, et al.
Pageof 77

Showing results (541-550 of 766) with videos related to

Sort By:
Pageof 77
The Journal of Clinical Investigation|December 1, 1991
Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitA K Gupta, K A Kirchner, R Nicholson, et al.
American Journal of Hematology|October 11, 2007
Sickle cell bone disease: response to vitamin D and calciumAdeboye H Adewoye, Tai C Chen, Qianli Ma, et al.
American Journal of Hematology|November 14, 2008
Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobinIbifiri Wilcox, Kevin Boettger, Lance Greene, et al.
The American Journal of Cardiology|August 1, 1996
Dobutamine stress testing in the cardiac catheterization laboratoryS P Sedlis, J Lorin, A Matalon, et al.
Psychoneuroendocrinology|January 1, 1990
Endogenous opioids modulate the cardiovascular response to mental stressM Morris, P Salmon, H Steinberg, et al.
American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|June 21, 2014
Initial experience with the novel patent foramen ovale occlusion device Nit-Occlud® in patients with stroke or transient ischemic attackDaniel H Steinberg, Stefan C Bertog, Julia Momberger, et al.
Blood|April 15, 2011
Fetal hemoglobin in sickle cell anemiaIdowu Akinsheye, Abdulrahman Alsultan, Nadia Solovieff, et al.
Proteomics|May 3, 2002
An improved formulation of SYPRO Ruby protein gel stain: comparison with the original formulation and with a ruthenium II tris (bathophenanthroline disulfonate) formulationKiera N Berggren, Birte Schulenberg, Mary F Lopez, et al.
The American Journal of the Medical Sciences|August 1, 1992
Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoterM B Coleman, J G Adams, M W Plonczynski, et al.
Pageof 77