Abstract Background: The EVERREST Prospective Study is a multicentre observational cohort study of pregnancies affected by severe early-onset fetal growth restriction. The study recruits women with singleton pregnancies where the estimated fetal weight is less than the 3rd centile and below 600 g, between 20 + 0 and 26 + 6 weeks of pregnancy, in the absence of a known chromosomal, structural or infective cause. Method: The reported study was retrospective descriptive qualitative interview study of women who had participated in the EVERREST Prospective Study. The aim of this study was to explore the experiences and perceptions of pregnant women taking part in research during a pregnancy affected by severe early-onset fetal growth res...
Depictions of foetuses as fixed entities possessing personhood are powerful within public consciousn...
BACKGROUND: This study aimed to explore women's views on the acceptability of different techniques f...
Background: There is ambiguity with regard to what counts as an acceptable level of risk in clinical...
BACKGROUND: The EVERREST Prospective Study is a multicentre observational cohort study of pregnancie...
Background: The EVERREST Prospective Study is a multicentre observational cohort study of pregnancie...
Abstract Background: The EVERREST Prospective Study is a multicentre observational cohort study of ...
Background Fetal growth restriction (FGR) is a serious obstetric condition for which there is curre...
ObjectivesThe research team aimed to understand women's lived experiences during pregnancies with po...
Background: Fetal growth restriction (FGR) is a serious obstetric condition for which there is curre...
Background: Recruitment of pregnant women to population health research can be challenging, especial...
BACKGROUND: Bioethicists argue that inclusion of pregnant women in clinical research should be more ...
Background: The Midlands and North of England Stillbirth Study (MiNESS) was a case-control study of ...
Background: Bioethicists argue that inclusion of pregnant women in clinical research should be more ...
Abstract Background Bioethicists argue that inclusion of pregnant women in clinical research should ...
Aim: Pregnancy after the death of a baby is associated with numerous, varied psychological challenge...
Depictions of foetuses as fixed entities possessing personhood are powerful within public consciousn...
BACKGROUND: This study aimed to explore women's views on the acceptability of different techniques f...
Background: There is ambiguity with regard to what counts as an acceptable level of risk in clinical...
BACKGROUND: The EVERREST Prospective Study is a multicentre observational cohort study of pregnancie...
Background: The EVERREST Prospective Study is a multicentre observational cohort study of pregnancie...
Abstract Background: The EVERREST Prospective Study is a multicentre observational cohort study of ...
Background Fetal growth restriction (FGR) is a serious obstetric condition for which there is curre...
ObjectivesThe research team aimed to understand women's lived experiences during pregnancies with po...
Background: Fetal growth restriction (FGR) is a serious obstetric condition for which there is curre...
Background: Recruitment of pregnant women to population health research can be challenging, especial...
BACKGROUND: Bioethicists argue that inclusion of pregnant women in clinical research should be more ...
Background: The Midlands and North of England Stillbirth Study (MiNESS) was a case-control study of ...
Background: Bioethicists argue that inclusion of pregnant women in clinical research should be more ...
Abstract Background Bioethicists argue that inclusion of pregnant women in clinical research should ...
Aim: Pregnancy after the death of a baby is associated with numerous, varied psychological challenge...
Depictions of foetuses as fixed entities possessing personhood are powerful within public consciousn...
BACKGROUND: This study aimed to explore women's views on the acceptability of different techniques f...
Background: There is ambiguity with regard to what counts as an acceptable level of risk in clinical...