1. Arterio-Venous Malformations of the Nose: Combined Approach for a Successful Strategy. Issue 6 (September 2016) Authors: Almesberger, Daria; Manna, Francesco; Guarneri, Gianni Franco; Marchesi, Andrea; Parodi, Pier Camillo Journal: Journal of craniofacial surgery Issue: Volume 27:Issue 6(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Arterio-Venous Malformations of the Nose: Combined Approach for a Successful Strategy. Issue 6 (September 2016) Authors: Almesberger, Daria; Manna, Francesco; Guarneri, Gianni Franco; Marchesi, Andrea; Parodi, Pier Camillo Journal: Journal of craniofacial surgery Issue: Volume 27:Issue 6(2016) Page Start: 1524 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Gain‐of‐function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway. Issue 2 (9th December 2019) Authors: Andolfo, Immacolata; Rosato, Barbara Eleni; Manna, Francesco; De Rosa, Gianluca; Marra, Roberta; Gambale, Antonella; Girelli, Domenico; Russo, Roberta; Iolascon, Achille Journal: American journal of hematology Issue: Volume 95:Issue 2(2020:Feb.) Page Start: 188 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genotype‐phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients. Issue 12 (2nd October 2018) Authors: Andolfo, Immacolata; Russo, Roberta; Rosato, Barbara Eleni; Manna, Francesco; Gambale, Antonella; Brugnara, Carlo; Iolascon, Achille Journal: American journal of hematology Issue: Volume 93:Issue 12(2018:Dec.) Page Start: 1509 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Kinome multigenic panel identified novel druggable EPHB4‐V871I somatic variant in high‐risk neuroblastoma. Issue 11 (26th April 2020) Authors: Andolfo, Immacolata; Lasorsa, Vito A.; Manna, Francesco; Rosato, Barbara E.; Formicola, Daniela; Iolascon, Achille; Capasso, Mario Journal: Journal of cellular and molecular medicine Issue: Volume 24:Issue 11(2020) Page Start: 6459 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias. Issue 5 (24th February 2018) Authors: Russo, Roberta; Andolfo, Immacolata; Manna, Francesco; Gambale, Antonella; Marra, Roberta; Rosato, Barbara Eleni; Caforio, Paola; Pinto, Valeria; Pignataro, Piero; Radhakrishnan, Kottayam; Unal, Sule; Tomaiuolo, Giovanna; Forni, Gian Luca; Iolascon, Achille Journal: American journal of hematology Issue: Volume 93:Issue 5(2018:May) Page Start: 672 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis). Issue 10 (October 2015) Authors: Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; Shmukler, Boris E.; Gambale, Antonella; Vitiello, Giuseppina; De Rosa, Gianluca; Brugnara, Carlo; Alper, Seth L.; Snyder, L. Michael; Iolascon, Achille Journal: American journal of hematology Issue: Volume 90:Issue 10(2015:Oct.) Page Start: 921 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Targeted next generation sequencing identifies a novel β‐spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis. Issue 10 (29th July 2017) Authors: Al‐Riyami, Arwa Z.; Iolascon, Achille; Al‐Zadjali, Shoaib; Andolfo, Immacolata; Al‐Mammari, Sahima; Manna, Francesco; Al Rawas, AbdulHakim; King, May‐Jean; Russo, Roberta Journal: American journal of hematology Issue: Volume 92:Issue 10(2017:Oct.) Page Start: E607 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The BMP‐SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE‐A260S variant. Issue 11 (30th August 2019) Authors: Andolfo, Immacolata; Rosato, Barbara Eleni; Marra, Roberta; De Rosa, Gianluca; Manna, Francesco; Gambale, Antonella; Iolascon, Achille; Russo, Roberta Journal: American journal of hematology Issue: Volume 94:Issue 11(2019:Nov.) Page Start: 1227 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Uridine treatment normalizes the congenital dyserythropoietic anemia type II‐like hematological phenotype in a patient with homozygous mutation in the CAD gene. Issue 11 (19th August 2020) Authors: Russo, Roberta; Marra, Roberta; Andolfo, Immacolata; Manna, Francesco; De Rosa, Gianluca; Rosato, Barbara Eleni; Radhakrishnan, Kottayam; Fahey, Michael; Iolascon, Achille Journal: American journal of hematology Issue: Volume 95:Issue 11(2020:Nov.) Page Start: 1423 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗