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Jo Howard

Showing results (11-20 of 79) with videos related to

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Scandinavian Journal of Infectious Diseases|October 23, 2010
Community-acquired Salmonella bacteraemia in patients with sickle-cell disease 1969-2008: a single centre studyLucinda H Richards, Jo Howard, John L Klein
Expert Review of Pharmacoeconomics & Outcomes Research|August 13, 2009
Pain management and quality of life in sickle cell diseaseJo Howard, Veronica J Thomas, Heather M Rawle
The Cochrane Database of Systematic Reviews|April 21, 2017
Hydroxyurea (hydroxycarbamide) for sickle cell diseaseSarah J Nevitt, Ashley P Jones, Jo Howard
British Journal of Haematology|February 20, 2013
Low flow nocturnal oxygen therapy does not suppress haemoglobin levels or increase painful crises in sickle cell diseaseHugh Ip, Rachel Kesse-Adu, Jo Howard, et al.
British Journal of Haematology|December 19, 2014
Pregnancy outcome in patients with sickle cell disease in the UK--a national cohort study comparing sickle cell anaemia (HbSS) with HbSC diseaseEugene Oteng-Ntim, Benjamin Ayensah, Marian Knight, et al.
British Journal of Haematology|April 24, 2014
Evaluation of the validity of Hb A2 and mean corpuscular haemoglobin action values in antenatal screening for beta thalassaemia carriers in EnglandYvonne Daniel, Ronwyn Cartwright, Kristian Rennie, et al.
Molecular Ecology|April 18, 2024
How admixed captive breeding populations could be rescued using local ancestry informationDaniel J Lawson, Jo Howard-McCombe, Mark Beaumont, et al.
British Journal of Haematology|May 25, 2002
Mycophenolate mofetil for the treatment of refractory auto-immune haemolytic anaemia and auto-immune thrombocytopenia purpuraJo Howard, A Victor Hoffbrand, H Grant Prentice, et al.
Hemoglobin|July 30, 2011
Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotypeYvonne Daniel, Kim Hill, Baba Inusa, et al.
British Journal of Haematology|January 29, 2015
A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patientsKevin H M Kuo, Richard Ward, Banu Kaya, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Scandinavian Journal of Infectious Diseases|October 23, 2010
Community-acquired Salmonella bacteraemia in patients with sickle-cell disease 1969-2008: a single centre studyLucinda H Richards, Jo Howard, John L Klein
Expert Review of Pharmacoeconomics & Outcomes Research|August 13, 2009
Pain management and quality of life in sickle cell diseaseJo Howard, Veronica J Thomas, Heather M Rawle
The Cochrane Database of Systematic Reviews|April 21, 2017
Hydroxyurea (hydroxycarbamide) for sickle cell diseaseSarah J Nevitt, Ashley P Jones, Jo Howard
British Journal of Haematology|February 20, 2013
Low flow nocturnal oxygen therapy does not suppress haemoglobin levels or increase painful crises in sickle cell diseaseHugh Ip, Rachel Kesse-Adu, Jo Howard, et al.
British Journal of Haematology|December 19, 2014
Pregnancy outcome in patients with sickle cell disease in the UK--a national cohort study comparing sickle cell anaemia (HbSS) with HbSC diseaseEugene Oteng-Ntim, Benjamin Ayensah, Marian Knight, et al.
British Journal of Haematology|April 24, 2014
Evaluation of the validity of Hb A2 and mean corpuscular haemoglobin action values in antenatal screening for beta thalassaemia carriers in EnglandYvonne Daniel, Ronwyn Cartwright, Kristian Rennie, et al.
Molecular Ecology|April 18, 2024
How admixed captive breeding populations could be rescued using local ancestry informationDaniel J Lawson, Jo Howard-McCombe, Mark Beaumont, et al.
British Journal of Haematology|May 25, 2002
Mycophenolate mofetil for the treatment of refractory auto-immune haemolytic anaemia and auto-immune thrombocytopenia purpuraJo Howard, A Victor Hoffbrand, H Grant Prentice, et al.
Hemoglobin|July 30, 2011
Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotypeYvonne Daniel, Kim Hill, Baba Inusa, et al.
British Journal of Haematology|January 29, 2015
A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patientsKevin H M Kuo, Richard Ward, Banu Kaya, et al.
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