Carla Olivieri - Concepedia

Author

Carla Olivieri

Also Known As

C OLIVIERI, C Olivieri, C. Olivieri, Carla OLIVIERI, Carla Olivieri, Claire Blachier, G. Ganci, Jessen, Jaime, L Ronzoni, Olivieri, C.

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

University of Pavia Istituti di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo Fondazione Azienda Ospedaliera Ospedale Maggiore University of Insubria

About

Carla Olivieri is an author at University of Pavia specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	872
2	Public Health	2	2	93
3	Gastroenterology	2	2	83
4	Health Sciences	1	1	33
5	Epidemiology	1	1	39

Carla Olivieri

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network Gaëtan Lesca, Carla Olivieri, Nelly Burnichon, Genetics in Medicine Genotype-phenotype CorrelationsHereditary Hemorrhagic TelangiectasiaGenetic DisorderGeneticsGenetic Epidemiology	2007	224
Overlapping spectra of <i>SMAD4</i> mutations in juvenile polyposis (JP) and JP–HHT syndrome Carol J. Gallione, Arthur S. Aylsworth, Jill Beis, American Journal of Medical Genetics Part A	2010	147
High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia Elisabetta Buscarini, Cesare Danesino, H Plauchu, Ultrasound in Medicine & Biology HepatologyHereditary Hemorrhagic TelangiectasiaHigh PrevalencePathologyMedicine	2004	134
Natural History and Outcome of Hepatic Vascular Malformations in a Large Cohort of Patients with Hereditary Hemorrhagic Teleangiectasia Elisabetta Buscarini, Gioacchino Leandro, Dario Conte, Digestive Diseases and Sciences	2011	127
Doppler Ultrasonographic Grading of Hepatic Vascular Malformations in Hereditary Hemorrhagic Telangiectasia - Results of Extensive Screening Elisabetta Buscarini, Cesare Danesino, Carla Olivieri, Ultraschall in der Medizin - European Journal of Ultrasound	2004	118
Contrast echocardiography for pulmonary arteriovenous malformations screening: does any bubble matter? Pietro Gazzaniga, Elisabetta Buscarini, Gioacchino Leandro, European Journal of Echocardiography	2008	97
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 Rosangela Invernizzi, Federica Quaglia, Catherine Klersy, The Lancet Haematology Severe Recurrent EpistaxisHematologySurgeryBleeding DisorderMedicine	2015	92
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies Carla Olivieri, Fabio Pagella, L Semino, Journal of Human Genetics Allelic VariantHht Italian FamiliesMendelian DisorderGenetic DisorderGenetics	2007	65
Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes Cecilia Canzonieri, L. Centenara, Federica Ornati, Genetics in Medicine Hereditary Hemorrhagic TelangiectasiaGastroenterologyPathologyEndoscopic EvaluationMedicine	2013	65
Identification of 13 new mutations in the <i>ACVRL1</i> gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia Carla Olivieri Journal of Medical Genetics	2002	62

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