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Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa
by
Hume, Heather A
, Ware, Russell E
, Ndugwa, Christopher M
, Latham, Teresa S
, Lane, Adam
, John, Chandy C
, Nabaggala, Catherine
, Kasirye, Phillip
, Opoka, Robert O
in
Anemia
/ Body weight
/ Charitable foundations
/ Children
/ Clinical trials
/ Confidence intervals
/ Dosage
/ Double-blind studies
/ Drug dosages
/ Enrollments
/ Fetuses
/ Hemoglobin
/ Hydroxyurea
/ Laboratories
/ Malaria
/ Medical screening
/ Neutropenia
/ Ratios
/ Safety
/ Sickle cell anemia
/ Sickle cell disease
/ Statistical analysis
/ Thrombocytopenia
2020
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Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa
by
Hume, Heather A
, Ware, Russell E
, Ndugwa, Christopher M
, Latham, Teresa S
, Lane, Adam
, John, Chandy C
, Nabaggala, Catherine
, Kasirye, Phillip
, Opoka, Robert O
in
Anemia
/ Body weight
/ Charitable foundations
/ Children
/ Clinical trials
/ Confidence intervals
/ Dosage
/ Double-blind studies
/ Drug dosages
/ Enrollments
/ Fetuses
/ Hemoglobin
/ Hydroxyurea
/ Laboratories
/ Malaria
/ Medical screening
/ Neutropenia
/ Ratios
/ Safety
/ Sickle cell anemia
/ Sickle cell disease
/ Statistical analysis
/ Thrombocytopenia
2020
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Do you wish to request the book?
Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa
by
Hume, Heather A
, Ware, Russell E
, Ndugwa, Christopher M
, Latham, Teresa S
, Lane, Adam
, John, Chandy C
, Nabaggala, Catherine
, Kasirye, Phillip
, Opoka, Robert O
in
Anemia
/ Body weight
/ Charitable foundations
/ Children
/ Clinical trials
/ Confidence intervals
/ Dosage
/ Double-blind studies
/ Drug dosages
/ Enrollments
/ Fetuses
/ Hemoglobin
/ Hydroxyurea
/ Laboratories
/ Malaria
/ Medical screening
/ Neutropenia
/ Ratios
/ Safety
/ Sickle cell anemia
/ Sickle cell disease
/ Statistical analysis
/ Thrombocytopenia
2020
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Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa
Journal Article
Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa
2020
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Overview
Hydroxyurea increases expression of fetal hemoglobin and decreases clinical complications in children with sickle cell anemia. A trial of a higher dose (30 mg per kg per day) as compared with a standard dose (20 mg per kg) in children in sub-Saharan Africa showed improved outcomes without increased toxicity.
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