(Q44117445)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

title

Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

hereditary hemorrhagic telangiectasia

2 March 2020

main subject

0 references

author

Carla Olivieri

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Federica Ornati

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

author name string

Cecilia Canzonieri

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Laura Centenara

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Fabio Pagella

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Elina Matti

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Costanza Alvisi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Cesare Danesino

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Maurizio Perego

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

language of work or name

English

0 references

publication date

30 May 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23722869%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

volume

16

1 reference

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2 March 2020

issue

1

1 reference

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2 March 2020

page(s)

3-10

1 reference

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Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment

2 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Hereditary haemorrhagic telangiectasia: a clinical and scientific review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Diagnosis and management of gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

High diagnostic and clinical impact of small-bowel capsule endoscopy in patients with hereditary hemorrhagic telangiectasia with overt digestive bleeding and/or severe anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Vascular, polypoid, and other lesions of the small bowel

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

History and development of capsule endoscopy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Bioinformatic analysis of pathogenic missense mutations of activin receptor like kinase 1 ectodomain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Pharmacological therapy of vascular malformations of the gastrointestinal tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Prevalence of colonic neoplasia and advanced lesions in the normal population: a prospective population-based colonoscopy study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Does any lower gastrointestinal bleeding in patients suffering from hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu) necessitate a full colonic visualization?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

Evidence of Small-Bowel Involvement in Hereditary Hemorrhagic Telangiectasia: a Capsule-Endoscopic Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

7 January 2021

Gastrointestinal lesions in hereditary hemorrhagic telangiectasia

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

7 January 2021

Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

7 January 2021

Evaluation of patients with hereditary hemorrhagic telangiectasia with video capsule endoscopy: a single-center prospective study

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

7 January 2021

Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.62

7 January 2021