Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Steinberg

Showing results (521-530 of 766) with videos related to

Pageof 77
Sort By:
The Journal of Clinical Investigation|May 1, 1979
Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemiaJ G Adams, L A Boxer, R L Baehner, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|June 19, 2012
Recurrent events after percutaneous closure of patent foramen ovaleJulia Wallenborn, Stefan C Bertog, Jennifer Franke, et al.
Hemoglobin|October 1, 1993
Beta-thalassemia in southwestern IranA Merat, M Haghshenas, Z M Pour, et al.
Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.
The Pharmacogenomics Journal|February 15, 2007
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyureaQ Ma, D F Wyszynski, J J Farrell, et al.
Hemoglobin|September 16, 2015
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC DiseaseAnthony O Akinbami, Andrew D Campbell, Zeqiu J Han, et al.
The Journal of Clinical Investigation|March 1, 1987
Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemiaM H Steinberg, J G Adams, W T Morrison, et al.
Investigative Ophthalmology & Visual Science|March 21, 1998
Protection of mouse photoreceptors by survival factors in retinal degenerationsM M LaVail, D Yasumura, M T Matthes, et al.
Research in Developmental Disabilities|January 9, 2025
What dimensions of school climate promote adaptive functioning in adolescents with ADHD? A prospective longitudinal studyElizabeth S M Chan, Cathrin D Green, Melissa R Dvorsky, et al.
Blood Cells, Molecules & Diseases|May 21, 2018
Biomarker signatures of sickle cell disease severityMengtian Du, Sarah Van Ness, Victor Gordeuk, et al.
Pageof 77

Showing results (521-530 of 766) with videos related to

Sort By:
Pageof 77
The Journal of Clinical Investigation|May 1, 1979
Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemiaJ G Adams, L A Boxer, R L Baehner, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|June 19, 2012
Recurrent events after percutaneous closure of patent foramen ovaleJulia Wallenborn, Stefan C Bertog, Jennifer Franke, et al.
Hemoglobin|October 1, 1993
Beta-thalassemia in southwestern IranA Merat, M Haghshenas, Z M Pour, et al.
Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.
The Pharmacogenomics Journal|February 15, 2007
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyureaQ Ma, D F Wyszynski, J J Farrell, et al.
Hemoglobin|September 16, 2015
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC DiseaseAnthony O Akinbami, Andrew D Campbell, Zeqiu J Han, et al.
The Journal of Clinical Investigation|March 1, 1987
Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemiaM H Steinberg, J G Adams, W T Morrison, et al.
Investigative Ophthalmology & Visual Science|March 21, 1998
Protection of mouse photoreceptors by survival factors in retinal degenerationsM M LaVail, D Yasumura, M T Matthes, et al.
Research in Developmental Disabilities|January 9, 2025
What dimensions of school climate promote adaptive functioning in adolescents with ADHD? A prospective longitudinal studyElizabeth S M Chan, Cathrin D Green, Melissa R Dvorsky, et al.
Blood Cells, Molecules & Diseases|May 21, 2018
Biomarker signatures of sickle cell disease severityMengtian Du, Sarah Van Ness, Victor Gordeuk, et al.
Pageof 77