(Q33592382)

28 July 2017

title

Osteoporosis-pseudoglioma syndrome with congenital heart disease: a new association (English)

1 reference

osteoporosis-pseudoglioma syndrome

28 July 2017

0 references

0 references

1 reference

based on heuristic

inferred from title

congenital heart disease

1 reference

1 reference

https://api.crossref.org/works/10.1136/JMG.25.1.32

30 December 2022

author name string

A. S. Teebi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

30 December 2022

S. A. Al-Awadi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

30 December 2022

M. J. Marafie

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

30 December 2022

R. A. Bushnaq

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

30 December 2022

S. Satyanath

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

30 December 2022

language of work or name

English

0 references

publication date

1 January 1988

1 reference

full work available at URL

28 July 2017

http://jmg.bmjjournals.com/cgi/content/abstract/25/1/32

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3351889/pdf/?tool=EBI

30 December 2022

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3351889/?tool=EBI

30 December 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

https://europepmc.org/articles/PMC1015419

30 December 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351889

https://europepmc.org/articles/PMC1015419?pdf=render

30 December 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%3A3351889

https://syndication.highwire.org/content/doi/10.1136/jmg.25.1.32

30 December 2022

1 reference

https://api.crossref.org/works/10.1136/JMG.25.1.32

Journal of Medical Genetics

30 December 2022

published in

1 reference

28 July 2017

volume

25

1 reference

28 July 2017

issue

1

1 reference

28 July 2017

page(s)

32-36

1 reference

The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

Osteoporosis-pseudoglioma or osteogenesis imperfecta?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

Osteoporosis-pseudoglioma syndrome: report of three affected sibs and an overview.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

Autosomal recessive syndrome of pseudogliomatous blindness, osteoporosis and mild mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

[Bilateral pseudo-glioma with generalized osteoporosis: an autosomal recessive disease]

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

Hyaloretinal degeneration with osteoporosis and bone fragility. Pseudoglioma with bone fragility (author's transl)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

Syndrome of osteoporosis with pseudoglioma.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015419

[Hyaloid-retinal dysplasia (pseudoglioma) due to recessive autosomal heredity]

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3351889

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Atypical osteogenesis imperfecta: Lobstein's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3351889

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.25.1.32

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=3351889

30 December 2022

1 reference

28 July 2017

1 reference