(Q35196472)

7 August 2017

title

Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations (English)

1 reference

7 August 2017

1 reference

S S Kang

1

1 reference

7 August 2017

P W Wong

2

1 reference

7 August 2017

H G Bock

3

1 reference

7 August 2017

A Horwitz

4

1 reference

7 August 2017

A Grix

5

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 March 1991

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

48

1 reference

7 August 2017

issue

3

1 reference

7 August 2017

page(s)

546-551

1 reference

Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Surface markers on human T and B lymphocytes. I. A large population of lymphocytes forming nonimmune rosettes with sheep red blood cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Homocysteinemia due to folate deficiency

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Plasma homocysteine, a risk factor for vascular disease: plasma levels in health, disease, and drug therapy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: paradigm of pitfalls in phenotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Protein-Bound Homocyst(e)ine in Normal Subjects and in Patients with Homocystinuria

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Homocysteinemia, ischemic heart disease, and the carrier state for homocystinuria.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682989

Radioassay of serum folate

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1998340

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of homozygotes and heterozygotes with methylenetetrahydrofolate reductase deficiency

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1998340

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Thermolabile methylenetetrahydrofolate reductase in patients with coronary artery disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1998340

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1682989

1 reference

7 August 2017

1 reference