Rare bone diseases and their dental, oral, and craniofacial manifestations (Q33936546)

30 July 2017

Rare bone diseases and their dental, oral, and craniofacial manifestations (English)

1 reference

30 July 2017

B L Foster

1

1 reference

30 July 2017

M S Ramnitz

2

1 reference

30 July 2017

R I Gafni

3

1 reference

30 July 2017

A B Burke

4

1 reference

30 July 2017

A M Boyce

5

1 reference

30 July 2017

J S Lee

6

1 reference

30 July 2017

J T Wright

7

1 reference

30 July 2017

S O Akintoye

8

1 reference

30 July 2017

M J Somerman

9

1 reference

30 July 2017

M T Collins

10

1 reference

30 July 2017

language of work or name

English

0 references

publication date

3 April 2014

1 reference

Journal of Dental Research

30 July 2017

1 reference

30 July 2017

93

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30 July 2017

7S-19S

1 reference

30 July 2017

7 Suppl

1 reference

Dental perspectives in fibrous dysplasia and McCune-Albright syndrome

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Bisphosphonate-related osteonecrosis of the jaws and its relevance to children--a review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Changing pattern of femoral fractures in osteogenesis imperfecta with prolonged use of bisphosphonates

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Gorham-Stout syndrome of the facial bones: a review of pathogenesis and treatment modalities and report of a case with a rare cutaneous manifestations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Recessively inherited forms of osteogenesis imperfecta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Tooth root dentin mineralization defects in a mouse model of hypophosphatasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Tumoral calcinosis: a dental literature review and case report

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Fassier-Duval femoral rodding in children with osteogenesis imperfecta receiving bisphosphonates: functional outcomes at one year

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

The surgical management of fibrous dysplasia of bone

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Osteogenesis Imperfecta: A Review with Clinical Examples.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Papilledema in the setting of x-linked hypophosphatemic rickets with craniosynostosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Miscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Vanishing bone disease: a review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Gorham-Stout disease: the experience of the Rizzoli Institute and review of the literature

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Treatment of Gorham-Stout disease with zoledronic acid and interferon-α: a case report and literature review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

X-linked hypophosphatemic rickets and craniosynostosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Neurosurgical aspects of childhood hypophosphatasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Age-dependent demise of GNAS-mutated skeletal stem cells and "normalization" of fibrous dysplasia of bone

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Enzyme replacement therapy for murine hypophosphatasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Pain in fibrous dysplasia of bone: age-related changes and the anatomical distribution of skeletal lesions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Onset, progression, and plateau of skeletal lesions in fibrous dysplasia and the relationship to functional outcome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Klotho converts canonical FGF receptor into a specific receptor for FGF23

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

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.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Polypeptide GalNAc-transferase T3 and familial tumoral calcinosis. Secretion of fibroblast growth factor 23 requires O-glycosylation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Osteoclastogenesis in fibrous dysplasia of bone: in situ and in vitro analysis of IL-6 expression

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Dental characteristics of fibrous dysplasia and McCune-Albright syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Hypophosphatasia and the role of alkaline phosphatase in skeletal mineralization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Progressive vertebral collapse in diffuse angiomatosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Genetic heterogeneity in osteogenesis imperfecta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Dentin structure in familial hypophosphatemic rickets: benefits of vitamin D and phosphate treatment.

5 July 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034514529150

Familial tumoral calcinosis caused by a novel FGF23 mutation: response to induction of tubular renal acidosis with acetazolamide and the non-calcium phosphate binder sevelamer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034514529150

Effect of intravenous pamidronate therapy on everyday activities in children with osteogenesis imperfecta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034514529150

Dental alterations associated with X-linked hypophosphatemic rickets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034514529150

Enzyme-replacement therapy in life-threatening hypophosphatasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034514529150

Dental implications of osteogenesis imperfecta: treatment with IV bisphosphonate: report of a case.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

Successful treatment of hyperphosphatemic tumoral calcinosis with long-term acetazolamide.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107543

The Gorham-Stout syndrome (Gorham's massive osteolysis). A report of six cases with histopathological findings

29 October 2018

1 reference

12 December 2020

The successful management of diffuse lymphangiomatosis using sirolimus: a case report

1 reference

12 December 2020

Normal vision despite narrowing of the optic canal in fibrous dysplasia

1 reference

12 December 2020

Dental lesions in tumoral calcinosis

1 reference

12 December 2020

Craniofacial morphology in patients with hypophosphatemic rickets: a cephalometric study focusing on differences between bone of cartilaginous and intramembranous origin

1 reference

12 December 2020

Clinical spectrum of hypophosphatasia diagnosed in adults

1 reference

12 December 2020

Intramedullary rodding in osteogenesis imperfecta

1 reference

12 December 2020

Cellular and humoral mechanisms of osteoclast formation and bone resorption in Gorham-Stout disease

1 reference

12 December 2020

Head and neck manifestations of tumoral calcinosis

1 reference

12 December 2020

Interleukin-6: a potential mediator of the massive osteolysis in patients with Gorham-Stout disease

1 reference

12 December 2020

Disappearing bone disease. A clinical and histological study

1 reference

12 December 2020

Wormian bones in osteogenesis imperfecta: Correlation to clinical findings and genotype

1 reference

12 December 2020

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis

1 reference

12 December 2020

Identifiers

DOI

10.1177/0022034514529150

1 reference

30 July 2017

1 reference

30 July 2017

1 reference