Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century. (Q35059330)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12566546%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

review article

1 reference

title

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century (English)

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17 December 2019

3

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17 December 2019

author name string

M E Begbie

series ordinal

1

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17 December 2019

G M F Wallace

series ordinal

2

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17 December 2019

language of work or name

English

0 references

publication date

1 January 2003

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Postgraduate Medical Journal

17 December 2019

published in

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17 December 2019

volume

79

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17 December 2019

issue

927

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17 December 2019

page(s)

18-24

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Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

17 December 2019

cites work

1 reference

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Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred

8 July 2018

1 reference

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A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1.

8 July 2018

1 reference

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Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Analysis of ALK-1 and endoglin in newborns from families with hereditary hemorrhagic telangiectasia type 2.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

A murine model of hereditary hemorrhagic telangiectasia

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Clinical outcome of transfemoral embolisation in patients with arteriovenous malformations of the liver in hereditary haemorrhagic telangiectasia (Weber-Rendu-Osler disease).

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Recanalization after coil embolotherapy of pulmonary arteriovenous malformations: study of long-term outcome and mechanism for recanalization

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

TGF-beta signalling from cell membrane to nucleus through SMAD proteins

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

A retrospective study of the role of the argon laser in the management of epistaxis secondary to hereditary haemorrhagic telangiectasia.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Medical complications of pregnancy in hereditary haemorrhagic telangiectasia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Laser ablation of upper gastrointestinal vascular ectasias: long term results

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Treatment of hereditary hemorrhagic telangiectasia by Nd-YAG laser photocoagulation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Hereditary haemorrhagic telangiectasia: a clinical analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Neurological manifestations of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): report of 2 cases and review of the literature

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Comparison of contrast echocardiography versus cardiac catheterization for detection of pulmonary arteriovenous malformations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Efficacy of unusually high doses of tranexamic acid for the treatment of epistaxis in hereditary hemorrhagic telangiectasia.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742589

Hereditary hemorrhagic telangiectasia; nine cases in one Negro family, with special reference to hepatic lesions

27 September 2018

1 reference

12 December 2020

Identification of hereditary hemorrhagic telangiectasia type 1 in newborns by protein expression and mutation analysis of endoglin

1 reference

12 December 2020

Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

Liver disease in patients with hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy

1 reference

12 December 2020

Bleeding from cerebral arteriovenous malformations as part of their natural history

1 reference

12 December 2020

Long-term results of dermatoplasty in the treatment of hereditary haemorrhagic telangiectasia

1 reference

12 December 2020

1 reference

12 December 2020

The natural history of epistaxis in hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

1 reference

12 December 2020

Brief report: treatment of bleeding in hereditary hemorrhagic telangiectasia with aminocaproic acid

1 reference

12 December 2020

Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings

1 reference

12 December 2020

Screening family members of patients with hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement

1 reference

12 December 2020

Caution with use of hepatic embolization in the treatment of hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

Identifiers

DOI

10.1136/PMJ.79.927.18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12566546%20AND%20SRC:MED&resulttype=core&format=json

release_2hfskgon7nctbisag6xfttuq3y

17 December 2019

Fatcat ID

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Fatcat

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24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12566546%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

PubMed publication ID

12566546

1 reference