Hereditary hemorrhagic telangiectasia (Q37151345)

18 August 2017

1 reference

title

Hereditary hemorrhagic telangiectasia. (English)

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hereditary hemorrhagic telangiectasia

18 August 2017

0 references

author name string

Anne Grand'Maison

series ordinal

1

1 reference

PMCID

2665965

18 August 2017

language of work or name

English

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publication date

1 April 2009

1 reference

Canadian Medical Association Journal

18 August 2017

1 reference

18 August 2017

180

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18 August 2017

8

1 reference

18 August 2017

833-835

1 reference

Hereditary hemorrhagic telangiectasia: epistaxis and hemoptysis

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary hemorrhagic telangiectasia: an overview of diagnosis and management in the molecular era for clinicians

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary haemorrhagic telangiectasia: a clinical analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary hemorrhagic telangiectasia: fatigue and dyspnea

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary hemorrhagic telangiectasia: transient ischemic attacks

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Pulmonary arteriovenous malformations. A state of the art review.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665965

Screening family members of patients with hereditary hemorrhagic telangiectasia

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19364792

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Embolotherapy of large pulmonary arteriovenous malformations: long-term results

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19364792

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: a family screening

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19364792

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1503/CMAJ.081739

1 reference

18 August 2017

1 reference

18 August 2017

1 reference

PMCID

2665965