Add to ORKGWe would like to extend special thanks to the following persons and groups: Children with sickle cell disease and their families for their constructive comment
Shortfalls in haemoglobinopathy provision result in patients and their carers receiving inadequate s...
Quality of assistance provided to children with sickle cell disease by primary healthcare service
Objective As technology advances, newborn screening will be possible for conditions not screened tod...
IntroductionDespite universal newborn screening (NBS), children in the U.S. continue to experience m...
The purpose of their review is to highlight the impacts this genetic condition has on patients as we...
Newborn screening (NBS) is intended to identify congenital conditions prior to the onset of symptoms...
Support from the national sickle cell disease program in the United States is resulting in significa...
Shortfalls in haemoglobinopathy provision result in patients and their carers receiving inadequate s...
This discussion paper has been written to show the unique contribution and added value that Patient ...
Persons with sickle cell trait (SCT) are heterozygous carriers of an abnormal f-globin gene that re...
Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the In...
Objective: To pilot a newborn screening program for sickle cell disease (SCD) in St. Vincent and the...
This chapter examines the rationale for sickle cell screening, including background, prevalence and ...
Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub...
Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub...
Shortfalls in haemoglobinopathy provision result in patients and their carers receiving inadequate s...
Quality of assistance provided to children with sickle cell disease by primary healthcare service
Objective As technology advances, newborn screening will be possible for conditions not screened tod...
IntroductionDespite universal newborn screening (NBS), children in the U.S. continue to experience m...
The purpose of their review is to highlight the impacts this genetic condition has on patients as we...
Newborn screening (NBS) is intended to identify congenital conditions prior to the onset of symptoms...
Support from the national sickle cell disease program in the United States is resulting in significa...
Shortfalls in haemoglobinopathy provision result in patients and their carers receiving inadequate s...
This discussion paper has been written to show the unique contribution and added value that Patient ...
Persons with sickle cell trait (SCT) are heterozygous carriers of an abnormal f-globin gene that re...
Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the In...
Objective: To pilot a newborn screening program for sickle cell disease (SCD) in St. Vincent and the...
This chapter examines the rationale for sickle cell screening, including background, prevalence and ...
Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub...
Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub...
Shortfalls in haemoglobinopathy provision result in patients and their carers receiving inadequate s...
Quality of assistance provided to children with sickle cell disease by primary healthcare service
Objective As technology advances, newborn screening will be possible for conditions not screened tod...