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Baba Inusa

Showing results (51-60 of 73) with videos related to

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Blood Advances|August 26, 2022
Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 yearsMohsen S Elalfy, Mona Hamdy, Amal El-Beshlawy, et al.
Blood Advances|August 10, 2022
Structural connectivity mediates the relationship between blood oxygenation and cognitive function in sickle cell anemiaJonathan D Clayden, Hanne Stotesbury, Jamie M Kawadler, et al.
British Journal of Haematology|October 22, 2016
Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and strokeMichael M Dowling, Charles T Quinn, Claudio Ramaciotti, et al.
Neurology|May 13, 2018
White matter integrity and processing speed in sickle cell anemiaHanne Stotesbury, Fenella J Kirkham, Melanie Kölbel, et al.
Journal of Racial and Ethnic Health Disparities|May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical ResearchAndrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
Trials|July 20, 2019
Prevention of Morbidity in Sickle Cell Disease (POMS2a)-overnight auto-adjusting continuous positive airway pressure compared with nocturnal oxygen therapy: a randomised crossover pilot study examining patient preference and safety in adults and childrenJo Howard, Sophie A Lee, Baba Inusa, et al.
Archives of Disease in Childhood|November 12, 2020
Clinical management of sickle cell liver disease in children and young adultsEirini Kyrana, David Rees, Florence Lacaille, et al.
The New England Journal of Medicine|December 9, 2015
A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive EventsMatthew M Heeney, Carolyn C Hoppe, Miguel R Abboud, et al.
Annals of Hematology|May 8, 2020
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysisCharles Antwi-Boasiako, Biree Andemariam, Raffaella Colombatti, et al.
Blood|October 14, 2010
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell diseaseMonica L Hulbert, Robert C McKinstry, JoAnne L Lacey, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Blood Advances|August 26, 2022
Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 yearsMohsen S Elalfy, Mona Hamdy, Amal El-Beshlawy, et al.
Blood Advances|August 10, 2022
Structural connectivity mediates the relationship between blood oxygenation and cognitive function in sickle cell anemiaJonathan D Clayden, Hanne Stotesbury, Jamie M Kawadler, et al.
British Journal of Haematology|October 22, 2016
Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and strokeMichael M Dowling, Charles T Quinn, Claudio Ramaciotti, et al.
Neurology|May 13, 2018
White matter integrity and processing speed in sickle cell anemiaHanne Stotesbury, Fenella J Kirkham, Melanie Kölbel, et al.
Journal of Racial and Ethnic Health Disparities|May 18, 2020
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical ResearchAndrew D Campbell, Raffaella Colombatti, Biree Andemariam, et al.
Trials|July 20, 2019
Prevention of Morbidity in Sickle Cell Disease (POMS2a)-overnight auto-adjusting continuous positive airway pressure compared with nocturnal oxygen therapy: a randomised crossover pilot study examining patient preference and safety in adults and childrenJo Howard, Sophie A Lee, Baba Inusa, et al.
Archives of Disease in Childhood|November 12, 2020
Clinical management of sickle cell liver disease in children and young adultsEirini Kyrana, David Rees, Florence Lacaille, et al.
The New England Journal of Medicine|December 9, 2015
A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive EventsMatthew M Heeney, Carolyn C Hoppe, Miguel R Abboud, et al.
Annals of Hematology|May 8, 2020
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysisCharles Antwi-Boasiako, Biree Andemariam, Raffaella Colombatti, et al.
Blood|October 14, 2010
Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell diseaseMonica L Hulbert, Robert C McKinstry, JoAnne L Lacey, et al.
Pageof 8