The National Newborn Screening Programme Summary of an audit of phenylketonuria and congenital hypothyroidism screening in England and Wales

NEWBORN SCREENING FOR RARE DISEASES IN THE NORTH-EAST PART OF ROMANIA: RESULTS OF THE NEWBORN SCREENING PROGRAM 2009-2012

Dana-Teodora Anton-Paduraru
Maria-Liliana Iliescu

December 2013

Objective. To evaluate the Newborn Screening Program for rare diseases – congenital hypothyroidism (...

107Newborn Screening in China—Xuefan Gu et al Newborn Screening in China: Phenylketonuria, Congenital Hypothyroidism and Expanded Screening

Xuefan Gu
Zhiguo Wang

January 2015

The diseases on the neonatal screening panel are difficult to diagnose by normal medical examination...

Newborn screening for inborn errors of metabolism: a systematic review.

Seymour
Thomason
Chalmers
Addison
Bain
Cockburn
Littlejohns
Lord
Wilcox

January 1997

: OBJECTIVES. To establish a database of literature and other evidence on neonatal screening program...

The National Newborn Screening Programme An audit of phenylketonuria and congenital hypothyroidism screening in England and Wales

Streetly, A.
Corbett, V.
United Medical and Dental Schools of Guy's and St. Thomas's Hospitals (UMDS)., London (United Kingdom). Dept. of Public Health Medicine

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:98/18094 / BLDSC - British Library Do...

Newborn screening for inborn errors of metabolism A systematic review

Seymour, C.
Thomason, M.
Chalmers, R.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1997

ReviewAvailable from British Library Document Supply Centre-DSC:4275.2242(1/11) / BLDSC - British Li...

Antenatal and neonatal haemoglobinopathy screening in the UK Review and economic analysis

Zeuner, D.
Ades, A.
Karnon, J.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1999

SIGLEAvailable from British Library Document Supply Centre-DSC:4275.2242(vol.3 no.11) / BLDSC - Brit...

Neonatal screening for inborn errors of metabolism Cost, yield and outcome

Pollitt, R.
Green, A.
McCabe, C.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:4275.2242(vol 1(7)) / BLDSC - British...

An audit of the thyroid screening programme in the Peninsula Maternal and Neonatal Services

Carrihill, Michelle Margaret

January 2008

Includes abstract.Includes bibliographical references (leaves 56-60).To audit the crod blood thryoid...

Evaluating newborn screening programmes based on dried blood spots: future challenges

Carol Dezateux

September 2016

A UK national programme to screen all newborn infants for phenylketonuria was introduced in 1969, fo...

Data: ‘Initial Clinical Referral Standards after Newborn Screening for Congenital Hypothyroidism: Final Report of the UK Newborn Screening Programme Centre Expert Working Group and Systematic Evidence Review 2010-2011’.

Rachel L. Knowles
Freyja Olafsdottir

July 2013

The multidisciplinary Expert Working Group was tasked with revising the existing standards of the UK...

SUMMARY

January 2008

Newborn screening for congenital hypothyroidism (CH) was implemented in Hospital UKM in December 200...

Torch screening reassessed The laboratory investigation of congenital, perinatal and neonatal infection

Sutherland, S.
Public Health Laboratory Service, London (United Kingdom)

January 1993

SIGLEAvailable from British Library Document Supply Centre-DSC:GPD/1160 / BLDSC - British Library Do...

Screening for congenital hypothyroidism in the Netherlands

Derksen-Lubsen, G.

January 1981

abstractScreening provides a means for 11filtering disease from the population11, until then unrecog...

Hypoglycaemia of the newborn Guidelines for appropriate blood glucose screening and treatment of breastfed and bottle fed babies in the United Kingdom

National Childbirth Trust, London (United Kingdom)

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:q97/25675 / BLDSC - British Library D...

Newborn screening for congenital hypothyroidism

Atilla Büyükgebiz

August 2016

In tro duc ti on Congenital hypothyroidism (CH) is the commonest treatable cause of mental retardati...

NEWBORN SCREENING FOR RARE DISEASES IN THE NORTH-EAST PART OF ROMANIA: RESULTS OF THE NEWBORN SCREENING PROGRAM 2009-2012

Dana-Teodora Anton-Paduraru
Maria-Liliana Iliescu

December 2013

Objective. To evaluate the Newborn Screening Program for rare diseases – congenital hypothyroidism (...

107Newborn Screening in China—Xuefan Gu et al Newborn Screening in China: Phenylketonuria, Congenital Hypothyroidism and Expanded Screening

Xuefan Gu
Zhiguo Wang

January 2015

The diseases on the neonatal screening panel are difficult to diagnose by normal medical examination...

Newborn screening for inborn errors of metabolism: a systematic review.

Seymour
Thomason
Chalmers
Addison
Bain
Cockburn
Littlejohns
Lord
Wilcox

January 1997

: OBJECTIVES. To establish a database of literature and other evidence on neonatal screening program...

The National Newborn Screening Programme An audit of phenylketonuria and congenital hypothyroidism screening in England and Wales

Streetly, A.
Corbett, V.
United Medical and Dental Schools of Guy's and St. Thomas's Hospitals (UMDS)., London (United Kingdom). Dept. of Public Health Medicine

January 1998

SIGLEAvailable from British Library Document Supply Centre-DSC:98/18094 / BLDSC - British Library Do...

Newborn screening for inborn errors of metabolism A systematic review

Seymour, C.
Thomason, M.
Chalmers, R.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1997

ReviewAvailable from British Library Document Supply Centre-DSC:4275.2242(1/11) / BLDSC - British Li...

Antenatal and neonatal haemoglobinopathy screening in the UK Review and economic analysis

Zeuner, D.
Ades, A.
Karnon, J.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1999

SIGLEAvailable from British Library Document Supply Centre-DSC:4275.2242(vol.3 no.11) / BLDSC - Brit...

Neonatal screening for inborn errors of metabolism Cost, yield and outcome

Pollitt, R.
Green, A.
McCabe, C.
National Coordinating Centre for Health Technology Assessment, Southampton (United Kingdom)

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:4275.2242(vol 1(7)) / BLDSC - British...

An audit of the thyroid screening programme in the Peninsula Maternal and Neonatal Services

Carrihill, Michelle Margaret

January 2008

Includes abstract.Includes bibliographical references (leaves 56-60).To audit the crod blood thryoid...

Evaluating newborn screening programmes based on dried blood spots: future challenges

Carol Dezateux

September 2016

A UK national programme to screen all newborn infants for phenylketonuria was introduced in 1969, fo...

Data: ‘Initial Clinical Referral Standards after Newborn Screening for Congenital Hypothyroidism: Final Report of the UK Newborn Screening Programme Centre Expert Working Group and Systematic Evidence Review 2010-2011’.

Rachel L. Knowles
Freyja Olafsdottir

July 2013

The multidisciplinary Expert Working Group was tasked with revising the existing standards of the UK...

SUMMARY

January 2008

Newborn screening for congenital hypothyroidism (CH) was implemented in Hospital UKM in December 200...

Torch screening reassessed The laboratory investigation of congenital, perinatal and neonatal infection

Sutherland, S.
Public Health Laboratory Service, London (United Kingdom)

January 1993

SIGLEAvailable from British Library Document Supply Centre-DSC:GPD/1160 / BLDSC - British Library Do...

Screening for congenital hypothyroidism in the Netherlands

Derksen-Lubsen, G.

January 1981

abstractScreening provides a means for 11filtering disease from the population11, until then unrecog...

Hypoglycaemia of the newborn Guidelines for appropriate blood glucose screening and treatment of breastfed and bottle fed babies in the United Kingdom

National Childbirth Trust, London (United Kingdom)

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:q97/25675 / BLDSC - British Library D...

Newborn screening for congenital hypothyroidism

Atilla Büyükgebiz

August 2016

In tro duc ti on Congenital hypothyroidism (CH) is the commonest treatable cause of mental retardati...

NEWBORN SCREENING FOR RARE DISEASES IN THE NORTH-EAST PART OF ROMANIA: RESULTS OF THE NEWBORN SCREENING PROGRAM 2009-2012

Dana-Teodora Anton-Paduraru
Maria-Liliana Iliescu

December 2013

Objective. To evaluate the Newborn Screening Program for rare diseases – congenital hypothyroidism (...

107Newborn Screening in China—Xuefan Gu et al Newborn Screening in China: Phenylketonuria, Congenital Hypothyroidism and Expanded Screening

Xuefan Gu
Zhiguo Wang

January 2015

The diseases on the neonatal screening panel are difficult to diagnose by normal medical examination...

Newborn screening for inborn errors of metabolism: a systematic review.

Seymour
Thomason
Chalmers
Addison
Bain
Cockburn
Littlejohns
Lord
Wilcox

January 1997

: OBJECTIVES. To establish a database of literature and other evidence on neonatal screening program...

The National Newborn Screening Programme Summary of an audit of phenylketonuria and congenital hypothyroidism screening in England and Wales

Abstract

Extracted data

The National Newborn Screening Programme Summary of an audit of phenylketonuria and congenital hypothyroidism screening in England and Wales

Abstract

Extracted data

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