(Q36061610)

11 August 2017

Phenylketonuria. Mass screening of newborns in Ireland (English)

1 reference

11 August 2017

1 reference

Cahalane SF

1

1 reference

PMC publication ID

2019828

11 August 2017

language of work or name

English

0 references

publication date

1 April 1968

1 reference

Archives of Disease in Childhood

11 August 2017

1 reference

11 August 2017

43

1 reference

11 August 2017

228

1 reference

11 August 2017

141-144

1 reference

Variations in intelligence in phenylktonuria

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

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.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019828

Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

23 September 2018

1 reference

12 December 2020

Screening program for early detection of phenylketonuria in the newborn in Israel

1 reference

12 December 2020

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

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

Atypical phenylketonuria in sisters with normal offspring

1 reference

12 December 2020

PHENYLKETONURIA: A REPORT ON THE GUTHRIE SCREENING TEST

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

NEWBORN PHENYLKETONURIA DETECTION PROGRAM IN MASSACHUSETTS

1 reference

12 December 2020

AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.43.228.141

1 reference

11 August 2017

1 reference

PMC publication ID

2019828

11 August 2017

PubMed publication ID

5645686

1 reference

PMC publication ID

2019828