Newborn bloodspot screening for cystic fibrosis is a valid public health strategy for populations with a high incidence of this inherited condition. There are a wide variety of approaches to screening and in this paper, we propose that a bioethical framework is required to determine the most appropriate screening protocol for a population. This framework depends on the detailed evaluation of the ethical consequences of all screening outcomes and placing these in the context of the genetic profile of the population screened, the geography of the region and the healthcare resources available
AbstractBackgroundFrench health authorities promoted a study on 553,167 newborns comparing the perfo...
Newborn screening (NBS) for cystic fibrosis (CF) offers the opportunity for early diagnosis and impr...
SUMMARY Practicable methods are now available for whole population screening of neonates for cystic ...
Since the late 1970s when the potential of the immunoreactive trypsinogen assay for early identifica...
The introduction and widespread implementation of newborn bloodspot screening (NBS) for cystic fibro...
AbstractBackgroundNewborn screening (NBS) for Cystic Fibrosis (CF) has been introduced in many count...
Newborn screening for cystic fibrosis offers the opportunity for early intervention and improved out...
Cystic Fibrosis (CF) newborn screening (NBS) has been controversial for many years in France; the lo...
Every newborn bloodspot screening (NBS) result for cystic fibrosis (CF) consists of two parts: a scr...
I have been involved in several areas of newborn screening, and my thesis deals with two of these: -...
Cystic fibrosis (CF) is a genetic disease that can be detected in newborn infants (i.e., those aged ...
Purpose of review: Cystic fibrosis screening in newborns is occurring in an increasing number of cou...
Newborn screening for cystic fibrosis (CF) is now universal in the US and many other countries. The ...
AbstractScreening newborns for cystic fibrosis (CF) is considered to be an ethical undertaking in re...
The different clinical manifestations of cystic fibrosis, with variable intensity and timing, often ...
AbstractBackgroundFrench health authorities promoted a study on 553,167 newborns comparing the perfo...
Newborn screening (NBS) for cystic fibrosis (CF) offers the opportunity for early diagnosis and impr...
SUMMARY Practicable methods are now available for whole population screening of neonates for cystic ...
Since the late 1970s when the potential of the immunoreactive trypsinogen assay for early identifica...
The introduction and widespread implementation of newborn bloodspot screening (NBS) for cystic fibro...
AbstractBackgroundNewborn screening (NBS) for Cystic Fibrosis (CF) has been introduced in many count...
Newborn screening for cystic fibrosis offers the opportunity for early intervention and improved out...
Cystic Fibrosis (CF) newborn screening (NBS) has been controversial for many years in France; the lo...
Every newborn bloodspot screening (NBS) result for cystic fibrosis (CF) consists of two parts: a scr...
I have been involved in several areas of newborn screening, and my thesis deals with two of these: -...
Cystic fibrosis (CF) is a genetic disease that can be detected in newborn infants (i.e., those aged ...
Purpose of review: Cystic fibrosis screening in newborns is occurring in an increasing number of cou...
Newborn screening for cystic fibrosis (CF) is now universal in the US and many other countries. The ...
AbstractScreening newborns for cystic fibrosis (CF) is considered to be an ethical undertaking in re...
The different clinical manifestations of cystic fibrosis, with variable intensity and timing, often ...
AbstractBackgroundFrench health authorities promoted a study on 553,167 newborns comparing the perfo...
Newborn screening (NBS) for cystic fibrosis (CF) offers the opportunity for early diagnosis and impr...
SUMMARY Practicable methods are now available for whole population screening of neonates for cystic ...