(Q39455018)

12 September 2017

Enzyme abnormalities in the porphyrias. (English)

1 reference

12 September 2017

M J Brodie

1

1 reference

12 September 2017

M R Moore

series ordinal

2

1 reference

12 September 2017

A Goldberg

series ordinal

3

1 reference

12 September 2017

language of work or name

English

0 references

publication date

1 October 1977

1 reference

12 September 2017

1 reference

12 September 2017

2

1 reference

12 September 2017

699-701

1 reference

12 September 2017

8040

1 reference

Assays for Porphyrins, δ-Aminolevulinic-Acid Dehydratase, and Porphyrinogen Synthetase in Microliter Samples of Whole Blood: Applications to Metabolic Defects Involving the Heme Pathway

12 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Decreased Red Cell Uroporphyrinogen I Synthetase Activity in Intermittent Acute Porphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Intermittent Acute Porphyria — Demonstration of a Genetic Defect in Porphobilinogen Metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Studies in porphyria. IV. Expression of the gene defect of acute intermittent porphyria in cultured human skin fibroblasts and amniotic cells: prenatal diagnosis of the porphyric trait

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Uroporphyrinogen III cosynthetase in asymptomatic carriers of congenital erythropoietic porphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Uroporphyrinogen III cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

The primary enzyme defect in hereditary coproporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Coproporphyrinogen-oxidase deficiency in hereditary coproporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Reduced ferrochelatase activity: a defect common to porphyria variegata and protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Conversion of coproporphyrinogen 3 to protoporphyrin IX

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Decreased Haem Synthetase Activity in Blood Cells of Patients with Erythropoietic Protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Porphyrin synthesis in blood cells of patients with erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

ACUTE INTERMITTENT PORPHYRIA: THE FIRST "OVERPRODUCTION DISEASE" LOCALIZED TO A SPECIFIC ENZYME

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Hepatic δ-Aminolaevulinic Acid Synthetase Activity in Symptomatic Porphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Activity of Amino-laevulinic Acid Synthetase in Normal and Porphyric Human Livers

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Acute intermittent porphyria. Increased ALA-synthetase activity during an acute attack

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Biochemical defects in two types of human hepatic porphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Hepatic -aminolaevulinic acid synthetase activity in porphyria cutanea tarda

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

The inhibition of red cell and brain ATPase by delta-aminolaevulinic acid.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

The effect of porphyrin precursors on monosynaptic reflex activity in the isolated hemisected frog spinal cord

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

Presynaptic neuromuscular inhibition by porphobilinogen and porphobilin

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2877%2990507-4

7 January 2021

10.1016/S0140-6736(77)90507-4

Identifiers

DOI

1 reference

12 September 2017

1 reference