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Swee Lay Thein

Showing results (131-140 of 203) with videos related to

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Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
Thorax|April 1, 2014
Pulmonary function, CT and echocardiographic abnormalities in sickle cell diseaseAlan Lunt, Sujal R Desai, Athol U Wells, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 20, 2021
Evaluation of Hepatic Iron Overload Using a Contemporary 0.55 T MRI SystemAdrienne E Campbell-Washburn, Christine Mancini, Anna Conrey, et al.
Blood|October 1, 2016
Reversible binding of hemoglobin to band 3 constitutes the molecular switch that mediates O2 regulation of erythrocyte propertiesHaiyan Chu, Mary M McKenna, Nathan A Krump, et al.
European Journal of Haematology|March 2, 2021
Long-term tolerability of phosphodiesterase-5 inhibitors in pulmonary hypertension of sickle cell diseaseCassondra Cramer-Bour, Amy Parker Ruhl, Seyed Mehdi Nouraie, et al.
British Journal of Haematology|November 12, 2005
Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climateSimon Jones, Edward R Duncan, Nikki Thomas, et al.
Haematologica|March 12, 2010
Extracranial internal carotid arterial disease in children with sickle cell anemiaColin R Deane, David Goss, Jack Bartram, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 29, 2007
Hepatic dysfunction in sickle cell disease: a new system of classification based on global assessmentPhilip A Berry, Timothy J S Cross, Swee Lay Thein, et al.
British Journal of Haematology|June 29, 2005
The measurement of urinary hydroxyurea in sickle cell anaemiaR Neil Dalton, Charles Turner, Moira Dick, et al.
British Journal of Haematology|January 6, 2009
Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobinLisa E Creary, Colin A McKenzie, Stephan Menzel, et al.
Pageof 21

Showing results (131-140 of 203) with videos related to

Sort By:
Pageof 21
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
Thorax|April 1, 2014
Pulmonary function, CT and echocardiographic abnormalities in sickle cell diseaseAlan Lunt, Sujal R Desai, Athol U Wells, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 20, 2021
Evaluation of Hepatic Iron Overload Using a Contemporary 0.55 T MRI SystemAdrienne E Campbell-Washburn, Christine Mancini, Anna Conrey, et al.
Blood|October 1, 2016
Reversible binding of hemoglobin to band 3 constitutes the molecular switch that mediates O2 regulation of erythrocyte propertiesHaiyan Chu, Mary M McKenna, Nathan A Krump, et al.
European Journal of Haematology|March 2, 2021
Long-term tolerability of phosphodiesterase-5 inhibitors in pulmonary hypertension of sickle cell diseaseCassondra Cramer-Bour, Amy Parker Ruhl, Seyed Mehdi Nouraie, et al.
British Journal of Haematology|November 12, 2005
Windy weather and low humidity are associated with an increased number of hospital admissions for acute pain and sickle cell disease in an urban environment with a maritime temperate climateSimon Jones, Edward R Duncan, Nikki Thomas, et al.
Haematologica|March 12, 2010
Extracranial internal carotid arterial disease in children with sickle cell anemiaColin R Deane, David Goss, Jack Bartram, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 29, 2007
Hepatic dysfunction in sickle cell disease: a new system of classification based on global assessmentPhilip A Berry, Timothy J S Cross, Swee Lay Thein, et al.
British Journal of Haematology|June 29, 2005
The measurement of urinary hydroxyurea in sickle cell anaemiaR Neil Dalton, Charles Turner, Moira Dick, et al.
British Journal of Haematology|January 6, 2009
Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobinLisa E Creary, Colin A McKenzie, Stephan Menzel, et al.
Pageof 21