(Q36966204)

17 August 2017

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title

Osteogenesis imperfecta:epidemiology and pathophysiology (English)

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17 August 2017

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Elizabeth Martin

1

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PubMed ID

17925189

17 August 2017

Jay R Shapiro

series ordinal

2

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17 August 2017

1 September 2007

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Current osteoporosis reports

17 August 2017

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17 August 2017

5

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17 August 2017

3

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17 August 2017

91-97

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https://scigraph.springernature.com/pub.10.1007/s11914-007-0023-z

17 August 2017

0 references

cites work

The birth prevalence rates for the skeletal dysplasias

1 reference

12 December 2020

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

1 reference

12 December 2020

On the paradoxically high relative prevalence of osteogenesis imperfecta type III in the black population of South Africa.

1 reference

12 December 2020

Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.

1 reference

12 December 2020

Pamidronate treatment of severe osteogenesis imperfecta in children under 3 years of age

1 reference

12 December 2020

Cell proliferation of human fibroblasts and osteoblasts in osteogenesis imperfecta: influence of age.

1 reference

12 December 2020

Classification of osteogenesis imperfect

1 reference

12 December 2020

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

1 reference

12 December 2020

Osteogenesis imperfecta type VII maps to the short arm of chromosome 3

1 reference

12 December 2020

Static and dynamic bone histomorphometry in children with osteogenesis imperfecta.

1 reference

12 December 2020

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

1 reference

12 December 2020

Osteogenesis imperfecta. A disease of the osteoblast

1 reference

12 December 2020

Osteogenesis imperfecta type III: an ancient mutation in Africa?

1 reference

12 December 2020

Osteogenesis imperfecta: a genetic, radiological, and epidemiological study.

1 reference

12 December 2020

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

12 December 2020

Pamidronate in children with osteogenesis imperfecta: histomorphometric effects of long-term therapy

1 reference

12 December 2020

Extracellular matrix formation by osteoblasts from patients with osteogenesis imperfecta.

1 reference

12 December 2020

Treatment of children with osteogenesis imperfecta

1 reference

12 December 2020

Type V osteogenesis imperfecta: a new form of brittle bone disease

1 reference

12 December 2020

The phenotypic spectrum of COL2A1 mutations

1 reference

12 December 2020

The effect of intravenous pamidronate on bone mineral density, bone histomorphometry, and parameters of bone turnover in adults with type IA osteogenesis imperfecta.

1 reference

12 December 2020

Effects of oral alendronate on BMD in adult patients with osteogenesis imperfecta: a 3-year randomized placebo-controlled trial

1 reference

12 December 2020

Osteogenesis imperfecta type VI in childhood and adolescence: effects of cyclical intravenous pamidronate treatment

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix

1 reference

12 December 2020

Cyclic administration of pamidronate in children with severe osteogenesis imperfecta

1 reference

12 December 2020

Osteogenesis imperfecta : current treatment options and future prospects

1 reference

12 December 2020

10.1007/S11914-007-0023-Z

Identifiers

DOI

1 reference

17 August 2017

1 reference

PubMed ID

17925189