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Journal Articles

Impact Of Liver Iron Overload On Myocardial T2* Response In Transfusion-Dependent Thalassemia Major Patients Treated With Deferasirox For Up To 3 Years

John Porter, MD, Ali T Taher, MD, Yesim Aydinok, MD, Maria D Cappellini, Antonis Kattamis, MD, Ali El-Ali, MD, Nicolas Martin, MS, Dudley Pennell, MD, FRCP

Blood (2013) 122 (21): 1016.

https://doi.org/10.1182/blood.V122.21.1016.1016

Published: 2013

Journal Articles

Serum Ferritin Levels and Morbidity in β-Thalassemia Intermedia: A 10-Year Cohort Study

Khaled M Musallam, MD, PhD, Maria D Cappellini, Shahina Daar, Mehran Karimi, Amal El-Beshlawy, Ali T Taher, MD

Blood (2012) 120 (21): 1021.

https://doi.org/10.1182/blood.V120.21.1021.1021

Published: 2012

Journal Articles

Spinal Artery Thrombosis: An Unrecognized Severe Complication in Thalassemia and Sickle Disorders

Maria Marzolini, Erika Poggiali, MD, Mohsin Badat, Elena Cassinerio, MD, Maria D Cappellini, John B. Porter, MD

Blood (2012) 120 (21): 1155.

https://doi.org/10.1182/blood.V120.21.1155.1155

Published: 2012

Journal Articles

Evaluation of the 5 Mg/g Liver Iron Concentration Threshold and Its Association with Vascular and Endocrine/Bone Morbidity in β-Thalassemia Intermedia

Khaled M Musallam, Maria D Cappellini, Ali T Taher, MD

Blood (2012) 120 (21): 1024.

https://doi.org/10.1182/blood.V120.21.1024.1024

Published: 2012

Journal Articles

Estimation of the Prevalence of Pulmonary Artery Hypertension in a Large Group of β-Thalassemia Patients Using Right Heart Catheterization

Giorgio Derchi, Renzo Galanello, MD, Patrizio Bina, Maria D Cappellini, Antonio Piga, MD, Maria-Eliana Lai, Antonella Quarta, Gavino Casu, Silverio Perrotta, Khaled M Musallam, Gian Luca Forni, MD

Blood (2012) 120 (21): 3262.

https://doi.org/10.1182/blood.V120.21.3262.3262

Published: 2012

Journal Articles

A Hepcidin Inhibitor Mobilizes Iron for Incorporation Into Red Blood Cells in an Adenine-Induced Chronic Kidney Disease Model in Rats.

Valentina Vaja, M.Sc., Chia Chi Sun, PhD, Maria D Cappellini, Herbert Yih-Fuu Lin, MD, PhD, Jodie L Babitt, MD

Blood (2012) 120 (21): 2082.

https://doi.org/10.1182/blood.V120.21.2082.2082

Published: 2012

Journal Articles

Determinants of Persisting Thrombocytopenia In Patients with Type 1 Gaucher Disease Treated with Alglucerase/Imiglucerase for 4–5 Years

Maria D. Cappellini, MD, Nadia Belmatoug, Alex Cole, Stephan vom Dahl, Patrick Deegan, Jack Goldblatt, Barry E. Rosenbloom, MD, Anna Tylki-Szymañska, Neal J. Weinreb, MD, Ari Zimran, MD, Carla Hollak, MD, PhD

Blood (2010) 116 (21): 4719.

https://doi.org/10.1182/blood.V116.21.4719.4719

Published: 2010

Journal Articles

Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study

Ali T. Taher, Khaled M. Musallam, Mehran Karimi, Amal El-Beshlawy, Khawla Belhoul, Shahina Daar, Mohamed-SalahEldin Saned, Abdul-Hamid El-Chafic, Maria R. Fasulo, Maria D. Cappellini

Blood (2010) 115 (10): 1886–1892.

https://doi.org/10.1182/blood-2009-09-243154

Published: 2010

Journal Articles

A Novel C to A Substitution in the CCAAT Box of beta Globin Gene.

Chiara Refaldi, PhD, Elena Di Pierro, Phd, Maria C. Mocellini, MD, Maria D. Cappellini, MD

Blood (2006) 108 (11): 3810.

https://doi.org/10.1182/blood.V108.11.3810.3810

Published: 2006

Journal Articles

Identification of a New Mutation in the 5′-UTR of Hepcidin Gene in beta-Thalassemia Major (TM) Patients.

Paola Delbini, PhD, Lorena Duca, PhD, Isabella Nava, PhD, Anna Meo, MD, Marina La Rosa, PhD, Maria D. Cappellini, MD

Blood (2006) 108 (11): 3811.

https://doi.org/10.1182/blood.V108.11.3811.3811

Published: 2006

Journal Articles

Expression of Hes-1 (Notch-1 Effector) during “ In Vitro ” Normal Erythroid Differentiation.

Maria D. Cappellini, MD, Ilaria V. Libani, BTD, Elisabetta Calzavara, BD, Luisa Ronzoni, BTD, Raffaella Chiaramonte, BD, Paola Comi, MD

Blood (2005) 106 (11): 4287.

https://doi.org/10.1182/blood.V106.11.4287.4287

Published: 2005

Journal Articles

Pharmacological Inhibition of K-Cl Cotransport Alters In Vitro Maturation of Normal and β-Thalassemic Human Erythroid Progenitors.

Lucia De Franceschi, MD, Luisa Ronzoni, Achille Iolascon, MD, Francesca Cimmino, Seth L. Alper, MD, PhD, Valeria Servedio, Franco Turrini, MD, Maria D. Cappellini, MD

Blood (2005) 106 (11): 3819.

https://doi.org/10.1182/blood.V106.11.3819.3819

Published: 2005

Journal Articles

Large Deletion of Chromosome 11 Causes Acute Intermittent Porphyria in an Italian Family.

Elena Di Pierro, PhD, Valeria Besana, BD, Valeria Moriondo, BD, Dario Tavazzi, PhD, Giovanna Casalgrande, PhD, Emilio Rocchi, MD, Maria D. Cappellini, MD

Blood (2005) 106 (11): 3543.

https://doi.org/10.1182/blood.V106.11.3543.3543

Published: 2005

Journal Articles

Two Functional Mutations in cis of the Ferrochelatase Gene (FECH) Cause Erythropoietic Protoporphyria (EPP).

Elena Di Pierro, PhD, Valentina Brancaleoni, BD, Valeria Moriondo, BtD, Maria D. Cappellini, MD

Blood (2005) 106 (11): 3544.

https://doi.org/10.1182/blood.V106.11.3544.3544

Published: 2005

Journal Articles

Proteomics of Membrane from Human Sickle and Normal Fractioned Red Cells Identifies Different Expression of Stress-Response Proteins.

Franco Turrini, MD, Franco Carta, Andrea Biondani, Paola Roncada, PhD, Maria D. Cappellini, MD, Roberto Corrocher, MD, Lucia De Franceschi, MD

Blood (2004) 104 (11): 3568.

https://doi.org/10.1182/blood.V104.11.3568.3568

Published: 2004

Journal Articles

Long-term treatment with oral sildenafil in a thalassemic patient with pulmonary hypertension

Roberto Littera, Giorgio La Nasa, Giorgio Derchi, Maria D. Cappellini, Christy Y. P. Chang, Licinio Contu

Blood (2002) 100 (4): 1516–1517.

https://doi.org/10.1182/blood-2002-04-1171

Published: 2002

NARROW

Impact Of Liver Iron Overload On Myocardial T2* Response In Transfusion-Dependent Thalassemia Major Patients Treated With Deferasirox For Up To 3 Years

Serum Ferritin Levels and Morbidity in β-Thalassemia Intermedia: A 10-Year Cohort Study

Spinal Artery Thrombosis: An Unrecognized Severe Complication in Thalassemia and Sickle Disorders

Evaluation of the 5 Mg/g Liver Iron Concentration Threshold and Its Association with Vascular and Endocrine/Bone Morbidity in β-Thalassemia Intermedia

Estimation of the Prevalence of Pulmonary Artery Hypertension in a Large Group of β-Thalassemia Patients Using Right Heart Catheterization

A Hepcidin Inhibitor Mobilizes Iron for Incorporation Into Red Blood Cells in an Adenine-Induced Chronic Kidney Disease Model in Rats.

Determinants of Persisting Thrombocytopenia In Patients with Type 1 Gaucher Disease Treated with Alglucerase/Imiglucerase for 4–5 Years

Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study

A Novel C to A Substitution in the CCAAT Box of beta Globin Gene.

Identification of a New Mutation in the 5′-UTR of Hepcidin Gene in beta-Thalassemia Major (TM) Patients.

Expression of Hes-1 (Notch-1 Effector) during “ In Vitro ” Normal Erythroid Differentiation.

Pharmacological Inhibition of K-Cl Cotransport Alters In Vitro Maturation of Normal and β-Thalassemic Human Erythroid Progenitors.

Large Deletion of Chromosome 11 Causes Acute Intermittent Porphyria in an Italian Family.

Two Functional Mutations in cis of the Ferrochelatase Gene (FECH) Cause Erythropoietic Protoporphyria (EPP).

Proteomics of Membrane from Human Sickle and Normal Fractioned Red Cells Identifies Different Expression of Stress-Response Proteins.

Long-term treatment with oral sildenafil in a thalassemic patient with pulmonary hypertension

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American Society of Hematology

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American Society of Hematology

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