(Q37866130)

24 August 2017

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title

Newborn screening: how are we travelling, and where should we be going? (English)

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24 August 2017

Bridget Wilcken

1

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24 August 2017

publication date

16 April 2011

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Journal of Inherited Metabolic Disease

24 August 2017

published in

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24 August 2017

volume

34

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24 August 2017

issue

3

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24 August 2017

page(s)

569-574

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Newborn screening: toward a uniform screening panel and system

24 August 2017

cites work

1 reference

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Development of a routine newborn screening protocol for severe combined immunodeficiency

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Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis

21 January 2018

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Molecular treatments in Duchenne muscular dystrophy

21 January 2018

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New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease

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Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany

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21 January 2018

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Protein misfolding in conformational disorders: rescue of folding defects and chemical chaperoning

21 January 2018

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Newborn screening of lysosomal storage disorders

21 January 2018

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Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism

21 January 2018

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Digital microfluidics: a future technology in the newborn screening laboratory?

21 January 2018

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Histidinaemia: Study of Relation Between Clinical and Biological Findings in 7 Subjects

21 January 2018

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Newborn screening in the Asia Pacific region

21 January 2018

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Parental tolerance of false-positive newborn screening results.

21 January 2018

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21 January 2018

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Health and economic benefits of well-designed evaluations: some lessons from evaluating neuroblastoma screening.

21 January 2018

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The consequences of extended newborn screening programmes: do we know who needs treatment?

21 January 2018

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Screening newborns for inborn errors of metabolism by tandem mass spectrometry

21 January 2018

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Expanded newborn screening: outcome in screened and unscreened patients at age 6 years.

21 January 2018

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Neonatal screening for cystic fibrosis in Wisconsin

21 January 2018

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12 December 2020

DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screening

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12 December 2020

Routine immunization, India's Achilles heel.

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12 December 2020

Expanded newborn screening: reducing harm, assessing benefit

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12 December 2020

Cystic fibrosis: benefits and clinical outcome

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12 December 2020

Histidinaemia: screening, diagnosis, clinical picture, therapy

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12 December 2020

Direct-to-consumer genotyping: are we ready for a brave new world?

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12 December 2020

Introducing new screens: why are we all doing different things?

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12 December 2020

The clinical effectiveness and cost-effectiveness of enzyme replacement therapy for Gaucher's disease: a systematic review

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12 December 2020

Challenges in the clinical application of whole-genome sequencing

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12 December 2020

Experts demand major revisions of German gene diagnostics law

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12 December 2020

A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

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12 December 2020

Weighing the evidence for newborn screening for early-infantile Krabbe disease

1 reference

12 December 2020

10.1007/S10545-011-9326-4

Identifiers

DOI

1 reference

release_ojrpd2r4e5belhlc2eadrphuwa

24 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/ojrpd2r4e5belhlc2eadrphuwa

24 November 2022

mapped directly with Wikidata item

1 reference