(Q44832583)

6 December 2017

Homocysteine, factor VII and antithrombin III in subjects with different gene dosage for cystathionine beta-synthase (English)

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6 December 2017

L Brattström

1

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6 December 2017

B Israelsson

series ordinal

2

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6 December 2017

L Tengborn

series ordinal

3

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6 December 2017

B Hultberg

series ordinal

4

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6 December 2017

1 January 1989

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Journal of Inherited Metabolic Disease

6 December 2017

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6 December 2017

12

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6 December 2017

4

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6 December 2017

475-482

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https://scigraph.springernature.com/pub.10.1007/bf01802045

6 December 2017

0 references

cites work

Radioenzymic determination of homocysteine in plasma and urine

1 reference

12 December 2020

[Homocystinuria and factor VII deficiency]

1 reference

12 December 2020

Is absence of atheroma in Down syndrome due to decreased homocysteine levels?

1 reference

12 December 2020

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

1 reference

12 December 2020

A case of homocystinuria with low antithrombin activity (author's transl)

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12 December 2020

Cloning and screening with nanogram amounts of immunopurified mRNAs: cDNA cloning and chromosomal mapping of cystathionine beta-synthase and the beta subunit of propionyl-CoA carboxylase

1 reference

12 December 2020

Higher total plasma homocysteine in vitamin B12 deficiency than in heterozygosity for homocystinuria due to cystathionine beta-synthase deficiency

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12 December 2020

Homocystinuria. A type with vascular thrombosis and factor VII deficiency

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12 December 2020

Diet-responsive proconvertin (factor VII) deficiency in homocystinuria

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12 December 2020

DOES DOWN SYNDROME SUPPORT HOMOCYSTEINE THEORY OF ARTERIOSCLEROSIS?

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12 December 2020

Impaired homocysteine metabolism in early-onset cerebral and peripheral occlusive arterial disease. Effects of pyridoxine and folic acid treatment

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12 December 2020

Cystathionine beta synthase: gene dosage effect in trisomy 21

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12 December 2020

Assignment of the gene for cystathionine beta-synthase to human chromosome 21 in somatic cell hybrids

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12 December 2020

Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

1 reference

12 December 2020

Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiency

1 reference

12 December 2020

Factor VII deficiency and homocystinuria. Chance association or syndrome?

1 reference

12 December 2020

Down's syndrome: an atheroma-free model?

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12 December 2020

Letter: Antithrombin activity in homocystinuria

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12 December 2020

Blood coagulation changes in homocystinuria: effects of pyridoxine and other specific therapy

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01802045

1 reference

6 December 2017

1 reference