• 51 Citations
  • 4 h-Index
20112015
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Research Output 2011 2015

  • 51 Citations
  • 4 h-Index
  • 8 Article
2015
19 Citations (Scopus)
Hereditary Hemorrhagic Telangiectasia
Epistaxis
Thalidomide
Safety
Therapeutics
2014
9 Citations (Scopus)

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

Canzonieri, C., Centenara, L., Ornati, F., Pagella, F., Matti, E., Alvisi, C., Danesino, C., Perego, M. & Olivieri, C., Jan 2014, In : Genetics in Medicine. 16, 1, p. 3-10 8 p.

Research output: Contribution to journalArticle

Hereditary Hemorrhagic Telangiectasia
Gastrointestinal Tract
Genotype
Telangiectasis
Capsule Endoscopy

Hereditary haemorrhagic telangiectasia in North African and sub-Saharan patients

Canzonieri, C., Ornati, F., Matti, E., Chu, F., Manfredi, G., Olivieri, C., Buscarini, E. & Pagella, F., 2014, In : South African Medical Journal. 104, 4, p. 256-257 2 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)

Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia

Massa, M., Canzonieri, C., Campanelli, R., Ornati, F., Fois, G., Pagella, F., Matti, E., Buscarini, E., Danesino, C., Rosti, V. & Olivieri, C., 2014, In : International Journal of Hematology. 101, 1, p. 23-31 9 p.

Research output: Contribution to journalArticle

Hereditary Hemorrhagic Telangiectasia
Vascular Endothelial Growth Factor Receptor-2
Endothelial Cells
Hematopoietic Stem Cells
Mutation Rate
2013
7 Citations (Scopus)

Argon plasma coagulation is an effective treatment for hereditary hemorrhagic telangiectasia patients with severe nosebleeds

Pagella, F., Matti, E., Chu, F., Pusateri, A., Tinelli, C., Olivieri, C., Canzonieri, C., Boeri, L., Ornati, F. & Danesino, C., Feb 2013, In : Acta Oto-Laryngologica. 133, 2, p. 174-180 7 p.

Research output: Contribution to journalArticle

Argon Plasma Coagulation
Hereditary Hemorrhagic Telangiectasia
Epistaxis
Blood Transfusion
Therapeutics

Hereditary hemorrhagic telangiectasia: Breakpoint characterization of a novel large deletion in ACVRL1 suggests the causing mechanism

Boeri, L., Radi, O., Canzonieri, C., Buscarini, E., Scatigno, A., Minelli, A., Ornati, F., Pagella, F., Danesino, C. & Olivieri, C., Mar 2013, In : Molecular Syndromology. 4, 3, p. 119-124 6 p.

Research output: Contribution to journalArticle

Hereditary Hemorrhagic Telangiectasia
Ligation
Microsatellite Repeats
Polymerase Chain Reaction
Mutation
2011
12 Citations (Scopus)

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

Scotti, C., Olivieri, C., Boeri, L., Canzonieri, C., Ornati, F., Buscarini, E., Pagella, F. & Danesino, C., Oct 18 2011, In : PLoS One. 6, 10, e26431.

Research output: Contribution to journalArticle

Activin Receptors
activins
missense mutation
Gene encoding
Missense Mutation
2 Citations (Scopus)

Breast cancer and genetics

Boeri, L., Canzonieri, C., Cagioni, C., Ornati, F. & Danesino, C., Dec 2011, In : Journal of Ultrasound. 14, 4, p. 171-176 6 p.

Research output: Contribution to journalArticle

Breast Neoplasms
BRCA1 Gene
Genes
Penetrance
Genetic Counseling