(Q30794722)

English

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

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

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

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

0 references

1 reference

based on heuristic

inferred from title

author name string

Easey AJ

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Wallace GM

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Hughes JM

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Jackson JE

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Taylor WJ

5

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Shovlin CL

6

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

language of work or name

0 references

publication date

1 June 2003

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

74

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

6

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

743-748

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Arteriovenous malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Endovascular therapy of brain AVMs prior to radiosurgery.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Microsurgical treatment of arteriovenous malformations: analysis and comparison with stereotactic radiosurgery

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Intracranial cavernous malformations: lesion behavior and management strategies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Arteriovenous malformations of the brain: natural history in unoperated patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project 1981-86. 1. Methodology, demography and incident cases of first-ever stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

Decision analysis: a tool of the future: an application to unruptured arteriovenous malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

The natural history of symptomatic arteriovenous malformations of the brain: a 24-year follow-up assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

25 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

25 November 2018

The natural history of unruptured intracranial arteriovenous malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1738468

25 November 2018

Event, incidence and case fatality rates of cerebrovascular disease in Auckland, New Zealand

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Natural course of unoperated intracranial arteriovenous malformations: study of 50 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemorrhagic telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening family members of patients with hereditary hemorrhagic telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confidence limits made easy: interval estimation using a substitution method

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary arteriovenous malformations: effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bleeding from cerebral arteriovenous malformations as part of their natural history

1 reference

https://pubmed.ncbi.nlm.nih.gov/12754343

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.74.6.743

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

0 references

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