(Q64097322)

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10 April 2020

case report

0 references

title

Orthopedic Manifestations of Bruck Syndrome: A Case Series with Intermediate to Long-term Follow-Up (English)

1 reference

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10 April 2020

1 reference

6

1 reference

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10 April 2020

author name string

Adolfredo Santana

1

1 reference

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10 April 2020

Geovanny Oleas-Santillán

2

1 reference

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10 April 2020

Jeanne M Franzone

3

1 reference

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10 April 2020

L Reid Nichols

4

1 reference

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10 April 2020

J Richard Bowen

5

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10 April 2020

language of work or name

English

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publication date

13 March 2019

1 reference

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Case reports in orthopedics

10 April 2020

published in

1 reference

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10 April 2020

volume

2019

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10 April 2020

page(s)

8014038

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Creative Commons Attribution 4.0 International

10 April 2020

copyright license

start time

13 March 2019

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures.

1 reference

12 December 2020

Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2

1 reference

12 December 2020

1 reference

12 December 2020

Bruck syndrome: congenital joint contractures with bone fragility

1 reference

12 December 2020

A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient.

1 reference

12 December 2020

[Osteogenesis imperfecta: Treatment and results of a case series]

1 reference

12 December 2020

Osteogenesis imperfecta in adults

1 reference

12 December 2020

Bruck syndrome - a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation

1 reference

12 December 2020

Zoledronic acid in children with osteogenesis imperfecta and Bruck syndrome: a 2-year prospective observational study

1 reference

12 December 2020

Osteogenesis imperfecta

1 reference

12 December 2020

Advances in the Classification and Treatment of Osteogenesis Imperfecta

1 reference

12 December 2020

Effect of high-dose vitamin D supplementation on bone density in youth with osteogenesis imperfecta: A randomized controlled trial

1 reference

12 December 2020

Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.

1 reference

12 December 2020

Bone Material Properties in Osteogenesis Imperfecta

1 reference

12 December 2020

The Spine in Patients With Osteogenesis Imperfecta

1 reference

12 December 2020

The Rare Bone Disease Working Group: report from the 2016 American Society for Bone and Mineral Research Annual Meeting

1 reference

12 December 2020

Identifiers

DOI

10.1155/2019/8014038

1 reference

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10 April 2020

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10 April 2020

1 reference