1. P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE. (23rd June 2022) Authors: Rosato, B. E.; Alper, S. L.; Tomaiuolo, G.; Russo, R.; Iolascon, A.; Andolfo, I. Journal: HemaSphere Issue: Volume 6(2022)Supplement 3 Page Start: 1418 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. S283: ERN-EUROBLOODNET EUROPEAN REGISTRY OF PATIENTS AFFECTED BY RED BLOOD CELL DISORDERS AND COVID-19. (23rd June 2022) Authors: Velasco, P.; Longo, F.; Piolatto, A.; Bardón-Cancho, E. J.; Ponce-Salas, B.; Flevari, P.; Voskaridou, E.; Biemond, B. J.; Nur, E; Delaporta, P.; Besse-Hammer, T.; Ruiz-Llobet, A.; Raso, S.; Spasiano, A.; Guerzoni, M. E.; Beneitez-Pastor, D.; Dedeken, L.; Pepe, A.; Rosso, R.; Kunz, J. B. Journal: HemaSphere Issue: Volume 6(2022)Supplement 3 Page Start: 184 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. S278: EVALUATION OF THE MAIN REGULATORS OF SYSTEMIC IRON HOMEOSTASIS IN PYRUVATE KINASE DEFICIENCY. (23rd June 2022) Authors: Zaninoni, A.; Russo, R.; Marra, R.; Andolfo, I.; Fermo, E.; Marcello, A. P.; Consonni, D.; Eleni Rosato, B.; Martone, S.; Fattizzo, B.; Barcellini, W.; Iolascon, A.; Bianchi, P. Journal: HemaSphere Issue: Volume 6(2022)Supplement 3 Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. S273: EVIDENCE OF NONINFERIORITY OF MITAPIVAT VERSUS SPLENECTOMY IN MURINE HEREDITARY SPHEROCYTOSIS. (23rd June 2022) Authors: Matte', A.; Recchiuti, A.; Federti, E.; Kosinski, P. A.; Riccardi, V.; Iatcenko, I.; Dang, L.; Iolascon, A.; Russo, R.; Brugnara, C.; Janin, A.; Leboeuf, C.; Mohandas, N.; De Franceschi, L. Journal: HemaSphere Issue: Volume 6(2022)Supplement 3 Page Start: 174 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. P.12.6 GENETIC VARIANTS ASSOCIATED WITH ANAEMIA IN ADULT COELIAC PATIENTS: THE ROLE OF TMPRSS6 AND HFE. (24th February 2016) Authors: Imperatore, N.; Rispo, A.; De Falco, L.; Capone, P.; Bruno, M.; Gerbino, N.; Caporaso, N.; Iolascon, A.; Tortora, R. Journal: Digestive and liver disease Issue: Volume 48(2016)Supplement 2 Page Start: e186 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. P.10.4 THE ROLE OF TMPRSS6 VARIANT RS855791 IN IRON-REFRACTORY IRON DEFICIENCY ANAEMIA (IRIDA) IN CELIAC DISEASE. Issue 2 (15th March 2018) Authors: Imperatore, N.; Tortora, R.; De Falco, L.; Iolascon, A.; Gerbino, N.; Nudo, D.; Montesano, L.; Nastro, F.; Caporaso, N.; Rispo, A. Journal: Digestive and liver disease Issue: Volume 50:Issue 2(2018)Supplement Page Start: e229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Acquired spherocytic like anemia combined with ineffective erythropoiesis sustains anemia in patients with chronic hepatitis C infection receiving telaprevir or boceprevir-based triple therapy. (15th February 2015) Authors: Lupo, F.; Russo, R.; Iolascon, A.; Ieluzzi, D.; Toniutto, P.; Piovesan, S.; Raffetti, E.; Siciliano, A.; Matte', A.; Turrini, F.; Donato, F.; Alberti, A.; Zuliani, V.; Fattovich, G.; De Franceschi, L. Journal: Digestive and liver disease Issue: Volume 47(2015)Supplement 1 Page Start: e15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders. (18th March 2015) Authors: King, M.‐J.; Garçon, L.; Hoyer, J. D.; Iolascon, A.; Picard, V.; Stewart, G.; Bianchi, P.; Lee, S.‐H.; Zanella, A.; the International Council for Standardization in Haematology Journal: International journal of laboratory hematology Issue: Volume 37:Number 3(2015:Jun.) Page Start: 304 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia. (12th June 2017) Authors: Makis, A.; Georgiou, I.; Traeger‐Synodinos, J.; Chaliasos, N.; Grosso, M.; Gambale, A.; Iolascon, A. Journal: International journal of laboratory hematology Issue: Volume 39:Number 5(2017:Oct.) Page Start: e124 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗