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Author/Creator Olivieri, Carla

2. Different forms of pulmonary hypertension in a family with clinical and genetic evidence for hereditary hemorrhagic teleangectasia type 2. (1st June 2018)

Authors:
Greco, Alessandra; Plumitallo, Sara; Scelsi, Laura; Maggi, Giannantonio; Sobrero, Matteo; Turco, Annalisa; Raineri, Claudia; Arseni, Natalia; Cappelletti, Donata; Visconti, Luigi Oltrona; Pagella, Fabio; Spinozzi, Giuseppe; Ghio, Stefano; Olivieri, Carla; Danesino, Cesare
Journal:
Pulmonary circulation
Issue:
Volume 8:Number 4(2018)
Page Start:
1
Record Type:
Journal Article
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3. Different forms of pulmonary hypertension in a family with clinical and genetic evidence for hereditary hemorrhagic teleangectasia type 2. (June 2018)

Authors:
Greco, Alessandra; Plumitallo, Sara; Scelsi, Laura; Maggi, Giannantonio; Sobrero, Matteo; Turco, Annalisa; Raineri, Claudia; Arseni, Natalia; Cappelletti, Donata; Visconti, Luigi Oltrona; Pagella, Fabio; Spinozzi, Giuseppe; Ghio, Stefano; Olivieri, Carla; Danesino, Cesare
Journal:
Pulmonary circulation
Issue:
Volume 8:Number 4(2018)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. 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. Issue 11 (November 2015)

Authors:
Invernizzi, Rosangela; Quaglia, Federica; Klersy, Catherine; Pagella, Fabio; Ornati, Federica; Chu, Francesco; Matti, Elina; Spinozzi, Giuseppe; Plumitallo, Sara; Grignani, Pierangela; Olivieri, Carla; Bastia, Raffaella; Bellistri, Francesca; Danesino, Cesare; Benazzo, Marco; Balduini, Carlo L
Journal:
Lancet
Issue:
Volume 2:Issue 11(2015)
Page Start:
e465
Record Type:
Journal Article
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5. Fluorescein‐guided intraoperative endoscopy in patients with hereditary hemorrhagic telangiectasia: first impressions. Issue 3 (11th November 2016)

Authors:
Pagella, Fabio; Pusateri, Alessandro; Zaccari, Dario; Bongetta, Daniele; Zoia, Cesare; Spinozzi, Giuseppe; Olivieri, Carla; Matti, Elina
Journal:
International forum of allergy & rhinology
Issue:
Volume 7:Issue 3(2017:Mar.)
Page Start:
300
Record Type:
Journal Article
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6. Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago. Issue 8 (27th May 2022)

Authors:
Sbalchiero, Anna; Abu Hweij, Yasmin; Mazza, Tommaso; Buscarini, Elisabetta; Scotti, Claudia; Pagella, Fabio; Manfredi, Guido; Matti, Elina; Spinozzi, Giuseppe; Olivieri, Carla
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 8(2022)
Page Start:
n/a
Record Type:
Journal Article
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7. Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability. (26th December 2018)

Authors:
Valli, Roberto; Minelli, Antonella; Galbiati, Marta; D'Amico, Giovanna; Frattini, Annalisa; Montalbano, Giuseppe; Khan, Abdul W.; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela
Journal:
British journal of haematology
Issue:
Volume 184:Number 6(2019)
Page Start:
974
Record Type:
Journal Article
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