(Q55422467)

8 July 2018

title

Set of simple side-room urine tests for detection of inborn errors of metabolism. (English)

1 reference

8 July 2018

author name string

Buist NR

series ordinal

1

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8 July 2018

language of work or name

English

0 references

publication date

1 June 1968

1 reference

8 July 2018

number of pages

5

1 reference

inferred from page(s)

published in

The BMJ

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8 July 2018

volume

2

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8 July 2018

issue

5607

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8 July 2018

page(s)

745-749

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8 July 2018

Urinary screening tests in the prevention of mental deficiency

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Screening test for hydrindicuria.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Clinical variants of galactosemia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

A rapid assay for urinary porphyrins by thin-layer chromatography.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

CHRONIC ACIDOSIS DUE TO AN ERROR IN LACTATE AND PYRUVATE METABOLISM. REPORT OF TWO CASES.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

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.

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Isovaleric acidemia. Clinical features of a new genetic defect of leucine metabolism.

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991639

Separation of nucleotides, nucleosides, purines, pyrimidines and some pyrimidine degradation products by two-dimensional paper chromatography

12 August 2018

1 reference

12 December 2020

A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency

1 reference

12 December 2020

A simple chromatographic screening test for the detection of galactosemia in newborn infants

1 reference

12 December 2020

Screen tests for metabolic disorders in newborn infants

1 reference

12 December 2020

Detection of metabolic disorders among mentally retarded children by means of paper spot tests

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

HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS

1 reference

12 December 2020

A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/BMJ.2.5607.745

1 reference

8 July 2018

PMC publication ID

1991639

1 reference

8 July 2018

PubMed publication ID

4231911

1 reference

8 July 2018