C. Olivieri

E. Buscarini, C. Olivieri, C. Danesino, 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Efficacy and safety of thalidomide for the treatment of severe recurrent epistaxis in hereditary haemorrhagic telangiectasia: results of a non-randomised, single-centre, phase 2 study.

C. Klersy, M. Benazzo, C. Olivieri, 2015, The Lancet. Haematology.

Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability

Abdul Waheed Khan, G. Montalbano, C. Olivieri, 2019, British journal of haematology.

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

C. Olivieri, C. Danesino, C. Alvisi, 2013, Genetics in Medicine.

Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience

C. Tinelli, C. Olivieri, S. Ugolini, 2021, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.

Hereditary Hemorrhagic Telangiectasia in Pediatric Age: Focus on Genetics and Diagnosis

C. Olivieri, C. Danesino, C. Cantarini, 2023, Pediatric reports.

Correlation of Severity of Epistaxis with Nasal Telangiectasias in Hereditary Hemorrhagic Telangiectasia (HHT) Patients

C. Tinelli, C. Olivieri, C. Danesino, 2009, American journal of rhinology & allergy.

ACVRL1 (activin A receptor type II-like 1)

C. Olivieri, L. Vecchia, C. Scotti, 2014 .

Characterization of a mutation in the zona pellucida module of Endoglin that causes Hereditary Hemorrhagic Telangiectasia.

P. Bayrak-Toydemir, L. Jovine, C. Olivieri, 2019, Gene.

Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP–HHT syndrome

Robert I. White, W. Reardon, B. Bernhardt, 2010, American journal of medical genetics. Part A.

Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia

E. Buscarini, V. Rosti, C. Olivieri, 2014, International Journal of Hematology.

Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism

E. Buscarini, C. Olivieri, C. Danesino, 2013, Molecular Syndromology.

Contrast echocardiography for pulmonary arteriovenous malformations screening: does any bubble matter?

C. Pedrinazzi, G. Inama, E. Buscarini, 2009, European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology.

Functional analysis of a novel ENG variant in a patient with hereditary hemorrhagic telangiectasia (HHT) identifies a new Sp1 binding-site.

Laura Scelsi, L. Scelsi, G. Babini, 2018, Gene.

Echocardiographic screening discloses increased values of pulmonary artery systolic pressure in 9 of 68 unselected patients affected with hereditary hemorrhagic telangiectasia

E. Buscarini, C. Olivieri, C. Danesino, 2006, Genetics in Medicine.

Interobserver agreement in diagnosing liver involvement in hereditary hemorrhagic telangiectasia by Doppler ultrasound.

R. Stefanov, M. Gebel, E. Buscarini, 2008, Ultrasound in medicine & biology.

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

E. Génin, E. Buscarini, F. Coulet, 2008, European Journal of Human Genetics.

Enhanced stem cells characteristic of fibroblastic mesenchymal cells from HHT patients

G. Magenes, G. Silvani, N. Crosetto, 2010 .

Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome.

V. Lisi, C. Olivieri, C. Danesino, 2002, Genetic counseling.

Nasal Endoscopy in the Clinical Diagnosis of Hereditary Hemorrhagic Telangiectasia.

A. de Silvestri, G. Marseglia, M. Benazzo, 2021, The Journal of pediatrics.

Immunohistochemical analysis of a merkeloma observed in a patient affected by hereditary haemorrhagic telangiectasia

E. Buscarini, V. Villanacci, E. Rossi, 2010, BMJ Case Reports.

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

F. Locatelli, M. Fabbri, G. Montalbano, 2018, Molecular Cytogenetics.

Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?

C. Olivieri, C. Danesino, M. Bozzola, 2004, Journal of endocrinological investigation.

Silicone septal splint for recurrent epistaxis in HHT patients: experience of a national referral centre

M. Benazzo, C. Olivieri, F. Sovardi, 2023, Acta Otorhinolaryngologica Italica.

Vascular abnormalities in the fingers of patients affected with hereditary hemorrhagic telangiectasia (HHT) as assessed by color doppler sonography

E. Buscarini, F. Draghi, C. Olivieri, 2005, American journal of medical genetics. Part A.

Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP–HHT syndrome

W. Reardon, B. Bernhardt, R. Pyeritz, 2010, American journal of medical genetics. Part A.

HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis

B. Wirnitzer, C. Olivieri, A. Lux, 2013, Orphanet Journal of Rare Diseases.

Activin Receptor-like kinase 1: a novel anti-angiogenesis target from TGF-β family.

C. Olivieri, L. Vecchia, C. Scotti, 2013, Mini reviews in medicinal chemistry.

Silicone septal splint for recurrent epistaxis in HHT patients: experience of a national referral centre

M. Benazzo, C. Olivieri, F. Sovardi, 2023, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.