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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

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

NARROW

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

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.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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