(Q64957612)

English

Popcorn calcification in osteogenesis imperfecta: incidence, progression, and molecular correlation.

scientific article published in November 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

Popcorn calcification in osteogenesis imperfecta: incidence, progression, and molecular correlation. (English)

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

osteogenesis imperfecta

0 references

author name string

Abimbola A Obafemi

1

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

Dorothy I Bulas

2

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

James Troendle

3

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

Joan C Marini

4

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

publication date

1 November 2008

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

American Journal of Medical Genetics

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

146A

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

21

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

2725-2732

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positive linear growth and bone responses to growth hormone treatment in children with types III and IV osteogenesis imperfecta: high predictive value of the carboxyterminal propeptide of type I procollagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Controlled trial of pamidronate in children with types III and IV osteogenesis imperfecta confirms vertebral gains but not short-term functional improvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Osteogenesis imperfecta--lower limb in osteogenesis imperfecta]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteogenesis imperfecta: A clinical study of the first ten years of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The morbid anatomy of the skeleton in osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Popcorn" calcifications: a prognostic sign in osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagens: molecular biology, diseases, and potentials for therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Osteogenesis imperfecta in childhood and adolescence]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.32508

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/6320686

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