Digital microfluidics: a future technology in the newborn screening laboratory? (Q33837219)

29 July 2017

title

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

1 reference

29 July 2017

0 references

5

Deeksha Bali

1 reference

29 July 2017

David S Millington

1

1 reference

29 July 2017

Ramakrishna Sista

2

1 reference

29 July 2017

Allen Eckhardt

3

1 reference

29 July 2017

Jeremy Rouse

4

1 reference

29 July 2017

Ronald Goldberg

6

1 reference

29 July 2017

Michael Cotten

7

1 reference

29 July 2017

Rebecca Buckley

8

1 reference

29 July 2017

Vamsee Pamula

9

1 reference

29 July 2017

publication date

1 April 2010

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29 July 2017

published in

Seminars in Perinatology

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29 July 2017

volume

34

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29 July 2017

issue

2

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29 July 2017

page(s)

163-169

1 reference

Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment

29 July 2017

cites work

1 reference

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Hyperbilirubinemia in the newborn infant > or =35 weeks' gestation: an update with clarifications

4 July 2018

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Heterogeneous immunoassays using magnetic beads on a digital microfluidic platform

4 July 2018

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Development of a digital microfluidic platform for point of care testing

4 July 2018

1 reference

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A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

4 July 2018

1 reference

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Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Development of population-based newborn screening for severe combined immunodeficiency

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

An integrated digital microfluidic lab-on-a-chip for clinical diagnostics on human physiological fluids

4 July 2018

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Enzyme replacement and enhancement therapies for lysosomal diseases

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Newborn screening for fragile X syndrome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

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

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

The application of tandem mass spectrometry to neonatal screening for inherited disorders of intermediary metabolism

4 July 2018

1 reference

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Science and society: genetic counselling and customary consanguineous marriage

4 July 2018

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The discovery of phenylketonuria: the story of a young couple, two retarded children, and a scientist

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Screening blood spots for inborn errors of metabolism by electrospray tandem mass spectrometry with a microplate batch process and a computer algorithm for automated flagging of abnormal profiles

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Universal bilirubin screening, guidelines, and evidence

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Development of a routine newborn screening protocol for severe combined immunodeficiency

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening program.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Electrowetting-based actuation of droplets for integrated microfluidics.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Electrowetting-based droplet mixers for microfluidic systems.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Biotinidase determination in serum and dried blood spots--high sensitivity fluorimetric ultramicro-assay

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866525

Rapid and effective screening for lysosomal storage disease: how close are we?

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20207266

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic and physiologic correlates of longitudinal immunoreactive trypsinogen decline in infants with cystic fibrosis identified through newborn screening

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20207266

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

NEWBORN PHENYLKETONURIA DETECTION PROGRAM IN MASSACHUSETTS

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20207266

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1053/J.SEMPERI.2009.12.008

1 reference

29 July 2017

1 reference

29 July 2017

1 reference