(Q36543037)

English

Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features

scientific article published on 27 June 2012

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scholarly article

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Europe PubMed Central

PMC publication ID

14 August 2017

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Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Ehlers-Danlos syndrome

0 references

connective tissue

1 reference

based on heuristic

inferred from title

periodontal disease

1 reference

based on heuristic

inferred from title

5

object named as

David L Rimoin

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1

object named as

Eyal Reinstein

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Celia Dawn DeLozier

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Ziv Simon

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Serguei Bannykh

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Cynthia J Curry

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

publication date

27 June 2012

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

European Journal of Human Genetics

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Europe PubMed Central

PMC publication ID

14 August 2017

21

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Europe PubMed Central

PMC publication ID

14 August 2017

2

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Europe PubMed Central

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14 August 2017

233-236

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Europe PubMed Central

PMC publication ID

14 August 2017

Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome--an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Periodontal Ehlers-Danlos syndrome associated with type III and I collagen deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Mendelian forms of periodontitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Treatment of periodontal disease in a patient with Ehlers-Danlos syndrome. A case report and literature review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos type VIII. Review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Intractable vasculitis, resorptive osteolysis, and immunity to type I collagen in type VIII Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos syndrome presenting with juvenile destructive periodontitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

30 September 2017

Ehlers-Danlos syndrome type VIII and leukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

28 June 2018

Molecular and cytologic studies of Ehlers-Danlos syndrome type VIII

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

28 June 2018

A distinct variant of the Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

28 June 2018

Early-onset osteoarthritis in Ehlers-Danlos syndrome type VIII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

21 September 2018

What syndrome is this? Ehlers-Danlos syndrome type VIII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

21 September 2018

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

21 September 2018

Localized aggressive periodontitis is linked to human chromosome 1q25.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548259

21 September 2018

Natural history and manifestations of the hypermobility type Ehlers-Danlos syndrome: A pilot study on 21 patients

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.132

21 January 2018

Ehlers-Danlos syndrome type VIII

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome type VIII: biochemical, stereological and immunocytochemical studies on dermis from a child with clinical signs of Ehlers-Danlos syndrome and a family history of premature loss of permanent teeth

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome identified from periodontal findings: case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome, type VIII presenting with periodontitis and prolonged bleeding time

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome type VIII: periodontitis, easy bruising, marfanoid habitus, and distinctive facies

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos type VIII, periodontitis-type: further delineation of the syndrome in a four-generation pedigree

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delineation of dermatan 4-O-sulfotransferase 1 deficient Ehlers-Danlos syndrome: observation of two additional patients and comprehensive review of 20 reported patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new variant of Ehlers-Danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring, and generalized periodontitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22739343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/EJHG.2012.132

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

0 references

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