1. A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene. (3rd May 2017) Authors: Noris, Patrizia; Marconi, Caterina; De Rocco, Daniela; Melazzini, Federica; Pippucci, Tommaso; Loffredo, Giuseppe; Giangregorio, Tania; Pecci, Alessandro; Seri, Marco; Savoia, Anna Journal: British journal of haematology Issue: Volume 181:Number 5(2018) Page Start: 698 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Identification of point mutations and large intragenic deletions in Fanconi anemia using next‐generation sequencing technology. Issue 6 (2nd July 2015) Authors: Nicchia, Elena; Greco, Chiara; De Rocco, Daniela; Pecile, Vanna; D'Eustacchio, Angela; Cappelli, Enrico; Corti, Paola; Marra, Nicoletta; Ramenghi, Ugo; Pillon, Marta; Farruggia, Piero; Dufour, Carlo; Pallavicini, Alberto; Torelli, Lucio; Savoia, Anna Journal: Molecular genetics & genomic medicine Issue: Volume 3:Issue 6(2015:Nov.) Page Start: 500 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Impaired immune response to Candida albicans in cells from Fanconi anemia patients. Issue 1 (May 2015) Authors: Parodi, Alessia; Kalli, Francesca; Svahn, Johanna; Stroppiana, Giorgia; De Rocco, Daniela; Terranova, Paola; Dufour, Carlo; Fenoglio, Daniela; Cappelli, Enrico Journal: Cytokine Issue: Volume 73:Issue 1(2015) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mutations of RUNX1 in families with inherited thrombocytopenia. Issue 6 (24th March 2017) Authors: De Rocco, Daniela; Melazzini, Federica; Marconi, Caterina; Pecci, Alessandro; Bottega, Roberta; Gnan, Chiara; Palombo, Flavia; Giordano, Paola; Coccioli, Maria Susanna; Glembotsky, Ana C.; Heller, Paula G.; Seri, Marco; Savoia, Anna; Noris, Patrizia Journal: American journal of hematology Issue: Volume 92:Issue 6(2017:Jun.) Page Start: E86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. MYH9 gene mutations associated with bleeding. (3rd April 2017) Authors: Savoia, Anna; De Rocco, Daniela; Pecci, Alessandro Journal: Platelets Issue: Volume 28:Number 3(2017) Page Start: 312 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. MYH9‐Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype–Phenotype Correlations. Issue 2 (12th December 2013) Authors: Pecci, Alessandro; Klersy, Catherine; Gresele, Paolo; Lee, Kieran J.D.; De Rocco, Daniela; Bozzi, Valeria; Russo, Giovanna; Heller, Paula G.; Loffredo, Giuseppe; Ballmaier, Matthias; Fabris, Fabrizio; Beggiato, Eloise; Kahr, Walter H.A.; Pujol‐Moix, Nuria; Platokouki, Helen; Van Geet, Christel; N... Journal: Human mutation Issue: Volume 35:Issue 2(2014:Feb.) Page Start: 236 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Somatic, hematologic phenotype, long‐term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Association of Pediatric Hematology–Oncology). Issue 7 (24th April 2016) Authors: Svahn, Johanna; Bagnasco, Francesca; Cappelli, Enrico; Onofrillo, Daniela; Caruso, Silvia; Corsolini, Fabio; De Rocco, Daniela; Savoia, Anna; Longoni, Daniela; Pillon, Marta; Marra, Nicoletta; Ramenghi, Ugo; Farruggia, Piero; Locasciulli, Anna; Addari, Carmen; Cerri, Carla; Mastrodicasa, Elena; C... Journal: American journal of hematology Issue: Volume 91:Issue 7(2016:Jul.) Page Start: 666 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Spectrum of the Mutations in Bernard–Soulier Syndrome. Issue 9 (15th July 2014) Authors: Savoia, Anna; Kunishima, Shinji; De Rocco, Daniela; Zieger, Barbara; Rand, Margaret L.; Pujol‐Moix, Nuria; Caliskan, Umran; Tokgoz, Huseyin; Pecci, Alessandro; Noris, Patrizia; Srivastava, Alok; Ward, Christopher; Morel‐Kopp, Marie‐Christine; Alessi, Marie‐Christine; Bellucci, Sylvia; Beurrier, P... Journal: Human mutation Issue: Volume 35:Issue 9(2014:Sep.) Page Start: 1033 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim. Issue 1 (30th November 2017) Authors: Pecci, Alessandro; Ragab, Iman; Bozzi, Valeria; De Rocco, Daniela; Barozzi, Serena; Giangregorio, Tania; Ali, Heba; Melazzini, Federica; Sallam, Mohamed; Alfano, Caterina; Pastore, Annalisa; Balduini, Carlo L; Savoia, Anna Journal: EMBO molecular medicine Issue: Volume 10:Issue 1(2018) Page Start: 63 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗