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

Oswaldo Castro

Showing results (31-40 of 44) with videos related to

Pageof 5
Sort By:
The American Journal of Cardiology|August 25, 2009
Prospective echocardiography assessment of pulmonary hypertension and its potential etiologies in children with sickle cell diseaseNiti Dham, Gregory Ensing, Caterina Minniti, et al.
Journal of the American College of Cardiology|January 30, 2007
Diastolic dysfunction is an independent risk factor for death in patients with sickle cell diseaseVandana Sachdev, Roberto F Machado, Yukitaka Shizukuda, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 19, 2008
Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) StudyChristine E McLaren, Victor R Gordeuk, Wen-Pin Chen, et al.
JAMA|July 20, 2006
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell diseaseRoberto F Machado, Anastasia Anthi, Martin H Steinberg, et al.
Diabetes Care|August 29, 2006
Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) studyRonald T Acton, James C Barton, Leah V Passmore, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|July 1, 2008
Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening studyRonald T Acton, James C Barton, Leah V Passmore, et al.
The Journal of Pediatrics|September 6, 2011
Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemiaDeepika S Darbari, Onyinye Onyekwere, Mehdi Nouraie, et al.
Human Molecular Genetics|February 8, 2017
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell diseaseXu Zhang, Binal N Shah, Wei Zhang, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) geneVictor R Gordeuk, Angela Caleffi, Elena Corradini, et al.
The New England Journal of Medicine|February 27, 2004
Pulmonary hypertension as a risk factor for death in patients with sickle cell diseaseMark T Gladwin, Vandana Sachdev, Maria L Jison, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
The American Journal of Cardiology|August 25, 2009
Prospective echocardiography assessment of pulmonary hypertension and its potential etiologies in children with sickle cell diseaseNiti Dham, Gregory Ensing, Caterina Minniti, et al.
Journal of the American College of Cardiology|January 30, 2007
Diastolic dysfunction is an independent risk factor for death in patients with sickle cell diseaseVandana Sachdev, Roberto F Machado, Yukitaka Shizukuda, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 19, 2008
Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) StudyChristine E McLaren, Victor R Gordeuk, Wen-Pin Chen, et al.
JAMA|July 20, 2006
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell diseaseRoberto F Machado, Anastasia Anthi, Martin H Steinberg, et al.
Diabetes Care|August 29, 2006
Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) studyRonald T Acton, James C Barton, Leah V Passmore, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|July 1, 2008
Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening studyRonald T Acton, James C Barton, Leah V Passmore, et al.
The Journal of Pediatrics|September 6, 2011
Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemiaDeepika S Darbari, Onyinye Onyekwere, Mehdi Nouraie, et al.
Human Molecular Genetics|February 8, 2017
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell diseaseXu Zhang, Binal N Shah, Wei Zhang, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) geneVictor R Gordeuk, Angela Caleffi, Elena Corradini, et al.
The New England Journal of Medicine|February 27, 2004
Pulmonary hypertension as a risk factor for death in patients with sickle cell diseaseMark T Gladwin, Vandana Sachdev, Maria L Jison, et al.
Pageof 5