(Q37076232)

18 August 2017

Cockayne's syndrome: case report (English)

1 reference

human chromosomes 6-12 and X

18 August 2017

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

26 March 2023

multiple abnormalities

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

26 March 2023

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

26 March 2023

1 reference

https://api.crossref.org/works/10.1136/JNNP.34.2.171

26 March 2023

author name string

L. Crome

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

26 March 2023

G. C. Kanjilal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

26 March 2023

language of work or name

English

0 references

publication date

1 April 1971

1 reference

PMC publication ID

493729

full work available at URL

18 August 2017

https://europepmc.org/articles/PMC493729

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

https://europepmc.org/articles/PMC493729?pdf=render

26 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4999043

https://syndication.highwire.org/content/doi/10.1136/jnnp.34.2.171

26 March 2023

1 reference

Crossref

https://api.crossref.org/works/10.1136/JNNP.34.2.171

Journal of Neurology, Neurosurgery and Psychiatry

26 March 2023

published in

1 reference

18 August 2017

34

1 reference

18 August 2017

2

1 reference

18 August 2017

171-178

1 reference

A syndrome resembling progeria: A review of two cases

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=493729

Microcephaly with extensive calcium deposits and demyelination

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=493729

The Neuropathology of Cockayne's Syndrome*†

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=493729

Cockayne's syndrome. An heredo-familial disorder of growth and development

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=493729

Cockayne's syndrome: Report of a case with hyperlipoproteinemia, hyperinsulinemia, renal disease, and normal growth hormone

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4999043

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Diffuse symmetric calcification in a syndrome including microcephaly and meningoencephalitis]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4999043

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

COCKAYNE'S SYNDROME. A REPORT OF FIVE NEW CASES WITH BIOCHEMICAL, CHROMOSOMAL, DERMATOLOGIC, GENETIC AND NEUROPATHOLOGIC OBSERVATIONS

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4999043

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dwarfism with retinal atrophy and deafness

2

1 reference

Crossref

https://api.crossref.org/works/10.1136/JNNP.34.2.171

Dwarfism with Retinal Atrophy and Deafness

26 March 2023

3

1 reference

Crossref

https://api.crossref.org/works/10.1136/JNNP.34.2.171

26 March 2023

Identifiers

1 reference

18 August 2017

1 reference

PMC publication ID

493729

18 August 2017

1 reference

PMC publication ID

493729