(Q39530091)

12 September 2017

Hyperlysinaemia. Harmless inborn error of metabolism? (English)

1 reference

12 September 2017

van Gelderen HH

1

1 reference

PMCID

1648636

12 September 2017

Teijema HL

series ordinal

2

1 reference

PMCID

1648636

12 September 2017

language of work or name

English

0 references

publication date

1 November 1973

1 reference

Archives of Disease in Childhood

12 September 2017

1 reference

12 September 2017

48

1 reference

12 September 2017

892-895

1 reference

12 September 2017

11

1 reference

Familial hyperlysinemia with lysine-ketoglutarate reductase insufficiency

12 September 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648636

13 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648636

A case of hyperlysinemia: biochemical and clinical observations

13 September 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648636

Hyperlysinemia associated with retardation

15 June 2018

1 reference

12 December 2020

Endogenous renal clearance rates of free amino acids in pre-pubertal children. (Employing an accelerated procedure for elution chromatography of basic amino acids on ion exchange resin)

1 reference

12 December 2020

Paths of lysine degradation in patients with hyperlysinemia

1 reference

12 December 2020

Further investigations in the methionine malabsorption syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.48.11.892

1 reference

12 September 2017

1 reference

12 September 2017

1 reference

PMCID

1648636