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Craniodiaphyseal dysplasia
scientific article
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instance of
scholarly article
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review article
1 reference
stated in
Europe PubMed Central
title
Craniodiaphyseal dysplasia
(English)
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author name string
L A Brueton
series ordinal
1
0 references
R M Winter
series ordinal
2
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language of work or name
English
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publication date
November 1990
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published in
Journal of Medical Genetics
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volume
27
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issue
11
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page(s)
701-6
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cites work
Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
27 September 2017
Craniodiaphyseal dysplasia, a disease or group of diseases?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
27 September 2017
Hydrocephalus and craniodiaphyseal dysplasia (author's transl)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
27 September 2017
Histologic, microradiographic and electron microscopic investigations of bone tissue in a case of craniodiaphyseal dysplasia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
27 September 2017
Dominantly inherited craniodiaphyseal dysplasia: a new craniotubular dysplasia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
30 May 2018
Craniodiaphyseal dysplasia. Partial suppression of osteoblastic activity in the severe progressive form with calcitonin therapy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
30 May 2018
Unusual case of hyperostosis of the type "cranio-diaphyseal dysplasia"
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
30 May 2018
On Paget's disease with leontiasis ossea and hypothyreosis, starting in early childhood.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017262
retrieved
29 November 2018
[A case of craniodiaphyseal dysplasia]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2277386
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Camurati-Engelmann disease (clinical and radiological contribution)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2277386
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hyperostosis corticalis generalisata. Report of seven cases
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2277386
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.27.11.701
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PMC publication ID
1017262
0 references
PubMed publication ID
2277386
0 references
ResearchGate publication ID
20879467
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