(Q34985625)

5 August 2017

title

Hereditary coproporphyria and epilepsy (English)

1 reference

hereditary coproporphyria

5 August 2017

main subject

1 reference

A. B. Houston

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

7 August 2022

M. J. Brodie

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

7 August 2022

M. R. Moore

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

7 August 2022

G. G. Thompson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

7 August 2022

J. B. Stephenson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

7 August 2022

language of work or name

English

0 references

publication date

1 August 1977

1 reference

full work available at URL

5 August 2017

https://europepmc.org/articles/PMC1544641

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

https://europepmc.org/articles/PMC1544641?pdf=render

7 August 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A921312

Archives of Disease in Childhood

7 August 2022

published in

1 reference

5 August 2017

volume

52

1 reference

5 August 2017

issue

8

1 reference

5 August 2017

page(s)

646-650

1 reference

Protein measurement with the Folin phenol reagent

5 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=1544641

PEDIATRIC ASPECTS OF THE PORPHYRIAS.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

Purification and properties of coproporphyrinogenase

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

Hereditary coproporphyria. Photosensitivity, jaundice and neuropsychiatric manifestations associated with pregnancy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

Acute intermittent porphyria in childhood. A neglected diagnosis?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

Childhood epileptic encephalopathy with slow spike-wave. A statistical study of 80 cases.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

Hereditary coproporphyria

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544641

The occurrence and determination of delta-amino-levulinic acid and porphobilinogen in urine

26 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary coproporphyria

1 reference

12 December 2020

Minor epileptic status

1 reference

12 December 2020

Diminished erythroid ferrochelatase activity in protoporphyria

1 reference

12 December 2020

Porphyria in childhood following transient neonatal quadriplegia

1 reference

12 December 2020

Hereditary coproporphyria. 7 cases

1 reference

12 December 2020

Biochemical defects in two types of human hepatic porphyria

1 reference

12 December 2020

Activities of delta-aminolevulinic acid synthetase in the liver and bone marrow of hepatic coproporphyria (hereditary coproporphyria)

1 reference

12 December 2020

Hereditary coproporphyria. A family with unusually few and mild symptoms

1 reference

12 December 2020

Hereditary coproporphyria. Study of a Swedish family

1 reference

12 December 2020

Delta-aminolaevulinic acid synthetase activity in normal and porphyric human livers

1 reference

12 December 2020

Acute intermittent porphyria with seizures. Anticonvulsant medication-induced metabolic changes

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.52.8.646

1 reference

5 August 2017

1 reference

5 August 2017

1 reference