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Prevalence of permanent childhood hearing loss detected at the universal newborn hearing screen: Systematic review and meta-analysis

PloS one, 2019-07, Vol.14 (7), p.e0219600-e0219600

2019

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Challenges for funders in monitoring compliance with policies on clinical trials registration and reporting: analysis of funding and registry data in the UK

BMJ open, 2020-02, Vol.10 (2), p.e035283-e035283

2020

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Modelling survival and mortality risk to 15 years of age for a national cohort of children with serious congenital heart defects diagnosed in infancy

PloS one, 2014-09, Vol.9 (8), p.e106806-e106806

2014

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Risk factors for permanent childhood hearing impairment

Archives of disease in childhood, 2020-02, Vol.105 (2), p.187

2020

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Unexpected deaths and unplanned re-admissions in infants discharged home after cardiac surgery: a systematic review of potential risk factors

Cardiology in the young, 2015-06, Vol.25 (5), p.839-852

2015

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Newborn Screening for Primary Congenital Hypothyroidism: Estimating Test Performance at Different TSH Thresholds

The journal of clinical endocrinology and metabolism, 2018-10, Vol.103 (10), p.3720-3728

2018

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Incidence, aetiology and neurodisability associated with severe microcephaly: a national surveillance study

Archives of disease in childhood, 2023-03, Vol.108 (3), p.211

2023

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Mortality with congenital heart defects in England and Wales, 1959–2009: exploring technological change through period and birth cohort analysis

Archives of disease in childhood, 2012-10, Vol.97 (10), p.861-865

2012

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Maternal ethnicity and the prevalence of British pregnancies affected by neural tube defects

Birth defects research, 2021-07, Vol.113 (12), p.968-980

2021

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Issues facing families of infants discharged after cardiac surgery: the perceptions of charity helpline staff

Acta Paediatrica, 2018-08, Vol.107 (8), p.1418-1426

2018

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Ethnic and socioeconomic variation in incidence of congenital heart defects

Archives of disease in childhood, 2017-06, Vol.102 (6), p.496

2017

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Ethnic-specific mortality of infants undergoing congenital heart surgery in England and Wales

Archives of disease in childhood, 2019-09, Vol.104 (9), p.844

2019

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Signs of deterioration in infants discharged home following congenital heart surgery in the first year of life: a qualitative study

Archives of disease in childhood, 2016-10, Vol.101 (10), p.902-908

2016

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Patient engagement in designing, conducting, and disseminating clinical pain research: IMMPACT recommended considerations

Pain (Amsterdam), 2024-05, Vol.165 (5), p.1013-1028

2024

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Sharing and reuse of individual participant data from clinical trials: principles and recommendations

BMJ open, 2017-12, Vol.7 (12), p.e018647-e018647

2017

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Patient-reported quality of life outcomes for children with serious congenital heart defects

Archives of disease in childhood, 2014-05, Vol.99 (5), p.413-419

2014

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Incidence and clinical features of congenital adrenal hyperplasia in Great Britain

Archives of disease in childhood, 2012-02, Vol.97 (2), p.101-106

2012

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Late clinical presentation of congenital adrenal hyperplasia in older children: findings from national paediatric surveillance

Archives of disease in childhood, 2014-01, Vol.99 (1), p.30-34

2014

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Ethics, governance and consent in the UK: implications for research into the longer-term outcomes of congenital heart defects

Archives of disease in childhood, 2011-01, Vol.96 (1), p.14-20

2011

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Surveillance of rare diseases: a public health evaluation of the British Paediatric Surveillance Unit

Journal of public health (Oxford, England), 2012-06, Vol.34 (2), p.279-286

2012

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Comparing the clinical and economic effects of clinical examination, pulse oximetry, and echocardiography in newborn screening for congenital heart defects: A probabilistic cost-effectiveness model and value of information analysis

International journal of technology assessment in health care, 2007-04, Vol.23 (2), p.192-204

2007

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Longer-term survival and health outcomes for children living with congenital heart defects

Paediatrics and child health, 2013-02, Vol.23 (2), p.73-77

2013

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Using multiple sources to improve and measure case ascertainment in surveillance studies: 20 years of the British Paediatric Surveillance Unit

Journal of public health (Oxford, England), 2006-06, Vol.28 (2), p.157-165

2006

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Quality of life and congenital heart defects: comparing parent and professional values

Archives of disease in childhood, 2007-05, Vol.92 (5), p.388-393

2007

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Infant deaths in the UK community following successful cardiac surgery: building the evidence base for optimal surveillance, a mixed-methods study

Health services and delivery research, 2016-05, Vol.4 (19), p.1-176

2016

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Prevalence of permanent childhood hearing loss detected at the universal newborn hearing screen: Systematic review and meta-analysis

Challenges for funders in monitoring compliance with policies on clinical trials registration and reporting: analysis of funding and registry data in the UK

Modelling survival and mortality risk to 15 years of age for a national cohort of children with serious congenital heart defects diagnosed in infancy

Risk factors for permanent childhood hearing impairment

Unexpected deaths and unplanned re-admissions in infants discharged home after cardiac surgery: a systematic review of potential risk factors

Newborn Screening for Primary Congenital Hypothyroidism: Estimating Test Performance at Different TSH Thresholds

Incidence, aetiology and neurodisability associated with severe microcephaly: a national surveillance study

Mortality with congenital heart defects in England and Wales, 1959–2009: exploring technological change through period and birth cohort analysis

Maternal ethnicity and the prevalence of British pregnancies affected by neural tube defects

Issues facing families of infants discharged after cardiac surgery: the perceptions of charity helpline staff

Ethnic and socioeconomic variation in incidence of congenital heart defects

Ethnic-specific mortality of infants undergoing congenital heart surgery in England and Wales

Signs of deterioration in infants discharged home following congenital heart surgery in the first year of life: a qualitative study

Patient engagement in designing, conducting, and disseminating clinical pain research: IMMPACT recommended considerations

Sharing and reuse of individual participant data from clinical trials: principles and recommendations

Patient-reported quality of life outcomes for children with serious congenital heart defects

Incidence and clinical features of congenital adrenal hyperplasia in Great Britain

Late clinical presentation of congenital adrenal hyperplasia in older children: findings from national paediatric surveillance

Ethics, governance and consent in the UK: implications for research into the longer-term outcomes of congenital heart defects

Surveillance of rare diseases: a public health evaluation of the British Paediatric Surveillance Unit

Comparing the clinical and economic effects of clinical examination, pulse oximetry, and echocardiography in newborn screening for congenital heart defects: A probabilistic cost-effectiveness model and value of information analysis

Longer-term survival and health outcomes for children living with congenital heart defects

Using multiple sources to improve and measure case ascertainment in surveillance studies: 20 years of the British Paediatric Surveillance Unit

Quality of life and congenital heart defects: comparing parent and professional values

Infant deaths in the UK community following successful cardiac surgery: building the evidence base for optimal surveillance, a mixed-methods study

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