(Q36062222)

11 August 2017

Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps (English)

1 reference

11 August 2017

0 references

G. R. Fraser

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

1 July 2023

A. I. Friedmann

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

1 July 2023

P. Maroteaux

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

1 July 2023

A. M. Glen-Bott

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

1 July 2023

U. Mittwoch

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

1 July 2023

language of work or name

English

0 references

publication date

1 August 1969

1 reference

PMC publication ID

2020135

full work available at URL

11 August 2017

https://europepmc.org/articles/PMC2020135

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5803642

https://europepmc.org/articles/PMC2020135?pdf=render

1 July 2023

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%3A5803642

https://syndication.highwire.org/content/doi/10.1136/adc.44.236.490

1 July 2023

1 reference

Crossref

https://api.crossref.org/works/10.1136/ADC.44.236.490

Archives of Disease in Childhood

1 July 2023

published in

1 reference

11 August 2017

44

1 reference

11 August 2017

236

1 reference

11 August 2017

490-498

1 reference

HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

FAMILIAL DWARFISM AND "STIFF JOINTS"

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

PATHOGENETIC CONSIDERATIONS ON A CASE OF MORQUIO-ULLRICH DISEASE

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

[Hurler's polydystrophy in a premature infant; associated with congenital cataract].

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

A newly recognized forme fruste of Hurler's disease (gargoylism)

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020135

A Childhood Syndrome of Bone Dysplasia, Retinal Detachment and Deafness

5 December 2018

1 reference

12 December 2020

[Metatrophic dwarfism]

1 reference

12 December 2020

[Differential diagnosis between dysostosis enchondralis and chondrodystrophy]

1 reference

12 December 2020

A hereditary factor in chondrodystrophia calcificans congenita

1 reference

12 December 2020

[Enchondralis dysostosis, type Bartenwerfer]

1 reference

12 December 2020

[Dominant heredity in a case of a polytopic enchondral dysostosis Pfaundler-Hurler type]

1 reference

12 December 2020

[Ehlers-Danlos and Brailsford-Morquio syndrome: nosologic correlations]

1 reference

12 December 2020

1 reference

12 December 2020

Ocular findings in Morquio-Ullrich's disease. With report of two cases

1 reference

12 December 2020

[Endochondral dysostosis (Bartenwerfer type).]

1 reference

12 December 2020

THE NATURAL HISTORY OF METAPHYSEAL DYSOSTOSIS

1 reference

12 December 2020

Dysplasia epiphysialis multiplex

5

1 reference

Crossref

https://api.crossref.org/works/10.1136/ADC.44.236.490

The Causes of Blindness in Childhood. A Study of 776 Children with Severe Visual Handicaps

1 July 2023

8

1 reference

Crossref

https://api.crossref.org/works/10.1136/ADC.44.236.490

1 July 2023

Identifiers

1 reference

11 August 2017

1 reference

PMC publication ID

2020135

11 August 2017

1 reference

PMC publication ID

2020135