(Q28364221)

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Detection of heterozygotes for homocystinuria. Study of sulphur-containing amino acids in plasma and urine after L-methionine loading

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Detection of heterozygotes for homocystinuria. Study of sulphur-containing amino acids in plasma and urine after L-methionine loading (English)

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I B Sardharwalla

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B Fowler

series ordinal

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A J Robins

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G M Komrower

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language of work or name

English

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publication date

July 1974

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published in

Archives of Disease in Childhood

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volume

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issue

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page(s)

553-9

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cites work

Chromatographic determination of cystine as cysteic acid

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

retrieved

29 September 2017

Treatment of homocystinuria

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

retrieved

29 September 2017

Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

retrieved

29 September 2017

Homocystinuria: Studies in Tissue Culture

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

retrieved

29 September 2017

Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

retrieved

2 June 2018

HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS.

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648915

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocystinuria: a report in two siblings

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methods for the quantitative analysis or sulphur-containing compounds in physiological fluids

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A modified procedure for the automatic analysis of amino acids

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ion exchange chromatography of amino acids--microdetermination of free amino acids in serum

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4851308

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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PubMed publication ID

4851308

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ResearchGate publication ID

18317987

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