(Q41762477)

9 October 2017

Mass screening of the newborn for metabolic disease (English)

1 reference

9 October 2017

L I Woolf

1

1 reference

PMC publication ID

2019823

9 October 2017

language of work or name

English

0 references

publication date

1 April 1968

1 reference

Archives of Disease in Childhood

9 October 2017

1 reference

9 October 2017

43

1 reference

9 October 2017

228

1 reference

9 October 2017

137-140

1 reference

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

9 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67).

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

Phenylketonuria. Mass screening of newborns in Ireland

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

6 June 2018

Phenylketonuria 1967.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

A NEW METHOD FOR THE DETECTION OF GALACTOXEMIA AND ITS CARRIER STATE

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019823

Legislation and advances in medical knowledge—acceleration or inhibition?

18 August 2018

1 reference

12 December 2020

Procedures for monitoring the low-phenylalanine diet in treatment of phenylketonuria

1 reference

12 December 2020

Use of micromethod for phenylalanine in management of phenylketonuric patients

1 reference

12 December 2020

A rapid method for the detection of plasma phenylalanine

1 reference

12 December 2020

AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE

1 reference

12 December 2020

The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England

1 reference

12 December 2020

A manual fluorometric paper disc method for detecting phenylketonuria

1 reference

12 December 2020

Diagnosis and treatment: interpreting the positive screening test in the newborn infant

1 reference

12 December 2020

Phenylalanine-hydroxylase activity in hyperphenylalaninaemia

1 reference

12 December 2020

APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.43.228.137

1 reference

9 October 2017

1 reference

PMC publication ID

2019823

9 October 2017

PubMed publication ID

5645685

1 reference

PMC publication ID

2019823