(Q83341070)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

Camurati-Engelmann disease: imaging, clinical features and differential diagnosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

Camurati-Engelmann disease

21 January 2020

main subject

1 reference

inferred from title

author name string

Aldona Bartuseviciene

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Arturas Samuilis

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Jovitas Skucas

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

publication date

12 February 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19214502%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

page(s)

1037-1043

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00256-008-0642-1

21 January 2020

exact match

0 references

cites work

Observations on the Camurati-Engelmann syndrome. Demonstration of changes of the petrous bone using high-resolution computed tomography

1 reference

12 December 2020

Asynchronous progressive diaphyseal dysplasia

1 reference

12 December 2020

Dominant endosteal hyperostosis. Skeletal characteristics and review of the literature

1 reference

12 December 2020

Ribbing's disease: radiographic-scintigraphic correlation and comparative analysis with Engelmann's disease

1 reference

12 December 2020

Familial hyperphosphatasemia: diagnosis in early infancy and response to human thyrocalcitonin therapy

1 reference

12 December 2020

Ribbing disease: a case report, a review of the literature, and a description of novel treatment

1 reference

12 December 2020

Progressive diaphyseal dysplasia (Camurati-Engelmann): radiographic follow-up and CT findings

1 reference

12 December 2020

Camurati-Engelmann disease. Review of radioclinical features.

1 reference

12 December 2020

Camurati-Engelmann disease: contribution of bone scintigraphy to genetic counseling

1 reference

12 December 2020

Sclerosing bone dysplasias ? a target-site approach

1 reference

12 December 2020

Camurati-Engelmann disease type II: progressive diaphyseal dysplasia with striations of the bones

1 reference

12 December 2020

Camurati-Engelmann disease--a case report and literature review

1 reference

12 December 2020

Engelmann's disease: a 45-year follow-up

1 reference

12 December 2020

Progessive diaphyseal dysplasia. Review of the literature and report of seven cases in one family

1 reference

12 December 2020

Intramedullary osteosclerosis: imaging features in nine patients

1 reference

12 December 2020

Sclerosing bone dysplasias: genetic and radioclinical features.

1 reference

12 December 2020

Van Buchem disease: lifetime evolution of radioclinical features

1 reference

12 December 2020

Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivity.

1 reference

12 December 2020

Endemic fluorosis of the skeleton: radiographic features in 127 patients

1 reference

12 December 2020

Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21

1 reference

12 December 2020

Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

1 reference

12 December 2020

[Camurati-Engelmann disease (progressive diaphyseal dysplasia). Differential diagnostic problems]

1 reference

12 December 2020

Case report 546: Endosteal hyperostosis (Worth type)

1 reference

12 December 2020

Hyperphosphatasia with massive osteoectasia: a 45-year follow-up.

1 reference

12 December 2020

Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family

1 reference

12 December 2020

Camurati-Engelmann disease: a late and sporadic case with metaphyseal involvement

1 reference

12 December 2020

Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.

1 reference

12 December 2020

Sclerosteosis. A case report

1 reference

12 December 2020