Fibrodysplasia ossificans progressiva: clinical and genetic aspects (Q35660697)

9 August 2017

1 reference

13 March 2019

Fibrodysplasia ossificans progressiva: clinical and genetic aspects (English)

1 reference

fibrodysplasia ossificans progressiva

9 August 2017

1 reference

13 March 2019

1 reference

Robert J Pignolo

1

1 reference

9 August 2017

Eileen M Shore

series ordinal

2

1 reference

9 August 2017

Frederick S Kaplan

series ordinal

3

1 reference

9 August 2017

language of work or name

1 reference

1 December 2011

2 references

Orphanet Journal of Rare Diseases

9 August 2017

13 March 2019

2 references

9 August 2017

13 March 2019

6

1 reference

9 August 2017

page(s)

80

1 reference

Creative Commons Attribution 2.0 Generic

9 August 2017

copyright license

1 reference

on focus list of Wikimedia project

13 March 2019

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

Early mortality and cardiorespiratory failure in patients with fibrodysplasia ossificans progressiva

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Early diagnosis of fibrodysplasia ossificans progressiva

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Proximal tibial osteochondromas in patients with fibrodysplasia ossificans progressiva

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Morphogen receptor genes and metamorphogenes: skeleton keys to metamorphosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Conductive hearing loss in individuals with fibrodysplasia ossificans progressiva

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Age- and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

Radiographic and scintigraphic features of modeling and remodeling in the heterotopic skeleton of patients who have fibrodysplasia ossificans progressiva.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3253727

The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22133093

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with Klippel-Feil syndrome: clues from the BMP signaling pathway

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22133093

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1750-1172-6-80

1 reference

Dimensions Publication ID

9 August 2017

0 references

1 reference

9 August 2017

1 reference