1. 416 DESMOPLAKIN CARDIOMYOPATHY PRESENTING WITH CARDIAC ARREST IN A PATIENT WITH MYOCARDIAL NON-COMPACTION AND LEFT ACCESSORY PATHWAY. (15th December 2022) Authors: Ragnatela, Ilaria; Santoro, Francesco; Vitale, Enrica; Cetera, Rosa; Santacroce, Rosa; Margaglione, Maurizio; Brunetti, Natale Daniele Journal: European heart journal supplements Issue: Volume 24(2022)Supplement K Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema. Issue 11 (1st July 2020) Authors: Ariano, Anastasia; D'Apolito, Maria; Bova, Maria; Bellanti, Francesco; Loffredo, Stefania; D'Andrea, Giovanna; Intrieri, Mariano; Petraroli, Angelica; Maffione, Angela Bruna; Spadaro, Giuseppe; Santacroce, Rosa; Margaglione, Maurizio Journal: Allergy Issue: Volume 75:Issue 11(2020) Page Start: 2989 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient. Issue 166 (June 2018) Authors: Viganò, Silvana; D'Andrea, Giovanna; Valle, Patrizia Della; Santacroce, Rosa; Margaglione, Maurizio; D'Angelo, Armando Journal: Thrombosis research Issue: Issue 166(2018) Page Start: 60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ABCB1 SNP rs4148738 modulation of apixaban interindividual variability. Issue 145 (September 2016) Authors: Dimatteo, Claudia; D'Andrea, Giovanna; Vecchione, Gennaro; Paoletti, Oriana; Tiscia, Giovanni Luca; Santacroce, Rosa; Correale, Michele; Brunetti, Natale; Grandone, Elvira; Testa, Sophie; Margaglione, Maurizio Journal: Thrombosis research Issue: Issue 145(2016) Page Start: 24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. ABCB1 SNP rs4148738 modulation of apixaban interindividual variability. Issue 145 (September 2016) Authors: Dimatteo, Claudia; D'Andrea, Giovanna; Vecchione, Gennaro; Paoletti, Oriana; Tiscia, Giovanni Luca; Santacroce, Rosa; Correale, Michele; Brunetti, Natale; Grandone, Elvira; Testa, Sophie; Margaglione, Maurizio Journal: Thrombosis research Issue: Issue 145(2016) Page Start: 24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Age of onset of cerebral venous thrombosis: the BEAST study. (March 2023) Authors: Ranjan, Redoy; Ken-Dror, Gie; Martinelli, Ida; Grandone, Elvira; Hiltunen, Sini; Lindgren, Erik; Margaglione, Maurizio; Le Cam Duchez, Veronique; Bagan Triquenot, Aude; Zedde, Marialuisa; Mancuso, Michelangelo; Ruigrok, Ynte M; Worrall, Brad; Majersik, Jennifer J; Putaala, Jukka; Haapaniemi, Elen... Journal: European stroke journal Issue: Volume 8:Number 1(2023) Page Start: 344 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Angiopoietin‐1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema. Issue 5 (19th February 2019) Authors: d'Apolito, Maria; Santacroce, Rosa; Colia, Anna Laura; Cordisco, Giorgia; Maffione, Angela Bruna; Margaglione, Maurizio Journal: Clinical & experimental allergy Issue: Volume 49:Issue 5(2019) Page Start: 626 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis. Issue 5 (29th September 2021) Authors: Ken‐Dror, Gie; Cotlarciuc, Ioana; Martinelli, Ida; Grandone, Elvira; Hiltunen, Sini; Lindgren, Erik; Margaglione, Maurizio; Duchez, Veronique Le Cam; Triquenot, Aude Bagan; Zedde, Marialuisa; Mancuso, Michelangelo; Ruigrok, Ynte M.; Marjot, Thomas; Worrall, Brad; Majersik, Jennifer J.; Metso, Tii... Journal: Annals of neurology Issue: Volume 90:Issue 5(2021) Page Start: 777 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of ten novel mutations in factor VIII gene: A study of a cohort of 52 haemophilia A patients. Issue 5 (May 2015) Authors: Santacroce, Rosa; Leccese, Angelica; Trunzo, Roberta; Lassandro, Giuseppe; Giordano, Paola; Ettorre, Cosimo; Antoncecchi, Stefano; Cantori, Isabella; Dragani, Alfredo; Belvini, Donata; Salviato, Roberta; Margaglione, Maurizio Journal: Thrombosis research Issue: Volume 135:Issue 5(2015) Page Start: 1031 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of ten novel mutations in factor VIII gene: A study of a cohort of 52 haemophilia A patients. Issue 5 (May 2015) Authors: Santacroce, Rosa; Leccese, Angelica; Trunzo, Roberta; Lassandro, Giuseppe; Giordano, Paola; Ettorre, Cosimo; Antoncecchi, Stefano; Cantori, Isabella; Dragani, Alfredo; Belvini, Donata; Salviato, Roberta; Margaglione, Maurizio Journal: Thrombosis research Issue: Volume 135:Issue 5(2015) Page Start: 1031 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗