List of works by Carla Olivieri

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

scientific article published on August 2013

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

article

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

scientific article published on 15 October 2012

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

scientific article

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

scientific article published on 11 January 2018

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

scientific article

Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms

scientific article published on 01 January 1998

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

scientific article

Correlation of severity of epistaxis with nasal telangiectasias in hereditary hemorrhagic telangiectasia (HHT) patients

scientific article published on January 2009

Correspondence

article published in 1999

Different forms of pulmonary hypertension in a family with clinical and genetic evidence for hereditary hemorrhagic teleangectasia type 2.

scientific article published on 25 May 2018

Doppler Ultrasonographic Grading of Hepatic Vascular Malformations in Hereditary Hemorrhagic Telangiectasia - Results of Extensive Screening

scientific article published on 01 September 2004

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

scientific article published on 01 March 2006

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

scientific article published on 27 October 2015

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

scientific article published on 30 May 2013

Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster.

scientific article

Familial partial monosomy 7 and myelodysplasia

scientific article published on 01 January 2001

Fluorescein-guided intraoperative endoscopy in patients with hereditary hemorrhagic telangiectasia: first impressions.

scientific article published on 11 November 2016

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

scientific article published on 3 January 2018

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

scientific article

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

scientific article published on 27 June 2013

Hereditary haemorrhagic telangiectasia in North African and sub-Saharan patients

scientific article published in April 2014

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

scientific article

High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia

scientific article published on 01 September 2004

Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia

scientific article

Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia.

scientific article published on 3 December 2014

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

scientific article published on 22 January 2008

Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders

scientific article published on 01 September 2000

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

scientific article published in January 2002

Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease.

scientific article

Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.

scientific article published in June 2001

Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.

scientific article

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

scientific article

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

scientific article published on 26 December 2018

Treatment of epistaxis in hereditary hemorrhagic telangiectasia patients by argon plasma coagulation with local anesthesia

scientific article published in July 2006

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

scientific article published on 01 May 2005

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