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Journal Articles

Evaluating the Clinical Impact of Hemoglobinopathy and Hereditary Red Blood Cell Disorder Co-Inheritance in a Cohort of 315 Patients

Filippo Russo, Anthony Iscaro, Roberta Marra, Antonella Nostroso, Barbara Eleni Rosato, Manuela Dionisi, Federica Maria Esposito, Vanessa D'Onofrio, Mariangela Manno, Valentina Brancaleoni, Simona Leoni, Achille Iolascon, Irene Motta, Immacolata Andolfo, Roberta Russo

Blood (2024) 144 (Supplement 1): 1069.

https://doi.org/10.1182/blood-2024-206878

Published: 2024

Journal Articles

pkm2 Binds to the Regulatory Regions of Gata-1 and stat5 in β-Thalassemic Mouse Erythroblasts

Enrica Federti, Silvia Pietrobono, Veronica Riccardi, Jacopo Ceolan, Richard Pozzetto Huot, Filippo Mazzi, Tolunay Kavaz, Immacolata Andolfo, Roberta Russo, Davide Melisi, Achille Iolascon, Lucia De Franceschi

Blood (2024) 144 (Supplement 1): 410.

https://doi.org/10.1182/blood-2024-203061

Published: 2024

Journal Articles

Single-Cell Transcriptomic Analysis of Bone Marrow from Humanized Sickle Cell Mice Reveals a Subpopulation of Highly-Expressing S100A8/A9 Mesenchymal Stem Cells

Jacopo Ceolan, Petros Kolovos, Enrica Federti, Panagiotis Liakopoulos, Veronica Riccardi, Immacolata Andolfo, Alessandro Mattè, Roberta Russo, Achille Iolascon, Helene Gleitz, Sjaak Philipsen, Lucia De Franceschi

Blood (2024) 144 (Supplement 1): 3867.

https://doi.org/10.1182/blood-2024-209911

Published: 2024

Journal Articles

PIEZO1 Gain-of-Function Variants Lead to Alterations in Late-Stage Erythropoiesis By Enhancing Enucleation Rate

Barbara Eleni Rosato, Antonella Nostroso, Vanessa D'Onofrio, Roberta Marra, Federica Maria Esposito, Vincenza Cerbone, Lucia De Franceschi, Achille Iolascon, Roberta Russo, Immacolata Andolfo

Blood (2024) 144 (Supplement 1): 3837.

https://doi.org/10.1182/blood-2024-204705

Published: 2024

Journal Articles

Unraveling the Role of PIEZO1 in Stressed Erythropoiesis: Implications for Dyserythropoiesis and Potential Therapeutic Targets in Dehydrated Hereditary Stomatocytosis

Barbara Eleni Rosato, Vanessa D'Onofrio, Antonella Nostroso, Roberta Marra, Federica Maria Esposito, Maddalena Raia, Giuseppe D'Alterio, Mario Capasso, Lucia De Franceschi, Achille Iolascon, Roberta Russo, Immacolata Andolfo

Blood (2023) 142 (Supplement 1): 2446.

https://doi.org/10.1182/blood-2023-180833

Published: 2023

Journal Articles

Colchicine Protects Against Cardiomyopathy in Humanized Mouse Model for Sickle Cell Disease

Enrica Federti, Iana Iatcenko, Alessandra Ghigo, Alessandro Mattè, Veronica Riccardi, Immacolata Andolfo, Angela Siciliano, Filippo Mazzi, Manuela Stella, Luigi Robbiano, Valeria Pinto, Achille Iolascon, Gian Luca Forni, Lucia De Franceschi

Blood (2022) 140 (Supplement 1): 2513–2514.

https://doi.org/10.1182/blood-2022-163037

Published: 2022

Journal Articles

Evaluation of the Main Regulators of Systemic Iron Homeostasis in Pyruvate Kinase Deficiency

Anna Zaninoni, Roberta Russo, Roberta Marra, Elisa Fermo, Immacolata Andolfo, Anna Paola Marcello, Dario Consonni, Barbara Eleni Rosato, Stefania Martone, Bruno Fattizzo, Wilma Barcellini, Achille Iolascon, Paola Bianchi

Blood (2021) 138 (Supplement 1): 1993.

https://doi.org/10.1182/blood-2021-151635

Published: 2021

Journal Articles

Nrf2 Plays a Key Role in Iron-Overload Cardiomyopathy

Enrica Federti, Francesca Vinchi, Iana Iatcenko, Alessandra Ghigo, Alessandro Mattè, Serge Cedrick, Angela Siciliano, Deborah Chiabrando, Emanuela Tolosano, S. Zebulon Vance, Veronica Riccardi, Immacolata Andolfo, Achille Iolascon, Lucia de Franceschi

Blood (2021) 138 (Supplement 1): 3068.

https://doi.org/10.1182/blood-2021-146157

Published: 2021

Journal Articles

PIEZO1 Mutation May Determine Early Onset of Clinical Manifestation of Anemia of Myelodysplastic Syndromes

Enrico Attardi, Immacolata Andolfo, Lucia Tiberi, Roberta Russo, Daniela Formicola, Alice Brogi, Marco Gabriele Raddi, Angela Consagra, Cristina Amato, Alessandro Sanna, Rosangela Artuso, Achille Iolascon, Valeria Santini

Blood (2021) 138 (Supplement 1): 1528.

https://doi.org/10.1182/blood-2021-149409

Published: 2021

Journal Articles

Congenital dyserythropoietic anemias

Achille Iolascon, Immacolata Andolfo, Roberta Russo

Blood (2020) 136 (11): 1274–1283.

https://doi.org/10.1182/blood.2019000948

Published: 2020

Journal Articles

The Novel Role That Nrf2 Plays in Erythropoiesis during Aging

Serge Cedrick Toya Mbiandjeu, Alessandro Mattè, BSc,PhD, Enrica Federti, PhD, Massimiliano Perduca, Immacolata Andolfo, Achille Iolascon, MD PhD, Maria Teresa Valenti, PhD, Arianna Pisani, Luca Dalle Carbonare, MD, Pietro Pucci, Angela Amoresano, Mohandas Narla, DSc, Lucia De Franceschi, MD

Blood (2019) 134 (Supplement_1): 3502.

https://doi.org/10.1182/blood-2019-125920

Published: 2019

Journal Articles

Resolution of sickle cell disease–associated inflammation and tissue damage with 17 R -resolvin D1

Alessandro Matte, Antonio Recchiuti, Enrica Federti, Bérengère Koehl, Thomas Mintz, Wassim El Nemer, Pierre-Louis Tharaux, Valentine Brousse, Immacolata Andolfo, Alessia Lamolinara, Olga Weinberg, Angela Siciliano, Paul C. Norris, Ian R. Riley, Achille Iolascon, Charles N. Serhan, Carlo Brugnara, Lucia De Franceschi

Blood (2019) 133 (3): 252–265.

https://doi.org/10.1182/blood-2018-07-865378

Published: 2019

Includes: Multimedia, Supplemental data

Journal Articles

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II

Roberta Russo, Immacolata Andolfo, Francesco Manna, Gianluca De Rosa, Luigia De Falco, Antonella Gambale, Mariasole Bruno, Alessandro Mattè, Paolo Ricchi, Domenico Girelli, Lucia De Franceschi, Achille Iolascon

Blood (2016) 128 (14): 1899–1902.

https://doi.org/10.1182/blood-2016-06-724328

Published: 2016

Includes: Supplemental data

Journal Articles

Detection of Familial Pseudohyperkalemia Among Italian Blood Donors By Genetic Screening for the R276W Mutation in ABCB6

Immacolata Andolfo, Roberta Russo, Francesco Manna, Marica Lisa Salve, Alok K. Sharma, Seth L. Alper, Lucia De Franceschi, MD, Achille Iolascon, MD PhD

Blood (2015) 126 (23): 2132.

https://doi.org/10.1182/blood.V126.23.2132.2132

Published: 2015

Journal Articles

Erfe-Encoding FAM132B in Congenital Dyserythropoietic Anemia Type II

Roberta Russo, Immacolata Andolfo, Luigia De Falco, Francesco Manna, Antonella Gambale, Mariasole Bruno, Gianluca De Rosa, Domenico Girelli, MD PhD, Lucia De Franceschi, MD, Achille Iolascon, MD PhD

Blood (2015) 126 (23): 535.

https://doi.org/10.1182/blood.V126.23.535.535

Published: 2015

Journal Articles

Dietary ω-3 Fatty Acid Supplementation As a Potential New Therapy for Vasculopathy in Sickle Cell Disease: Proof of Concept in a Transgenic Mouse Model

Brian T Kalish, MD, Alessandro Matte, PhD, Immacolata Andolfo, Achille Iolascon, Olga Weinberg, Angela Siciliano, Mrs, Enrica Federti, Mark Puder, MD PhD, Carlo Brugnara, MD, Lucia De Franceschi, MD

Blood (2014) 124 (21): 220.

https://doi.org/10.1182/blood.V124.21.220.220

Published: 2014

Journal Articles

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1

Blood (2013) 121 (19): 3925–3935.

https://doi.org/10.1182/blood-2013-02-482489

Published: 2013

Includes: Supplemental data

Journal Articles

Missense Mutations in the ABCB6 Transporter Cause Dominant Familial Pseudohyperkalemia

Immacolata Andolfo, Seth Alper, MD, PhD, Jean Delaunay, Carla Auriemma, Roberta Russo, Maria Rosaria Esposito, Alok K. Sharma, Boris E Shmukler, David H Vandorpe, Carlo Brugnara, M.D., Lucia De Franceschi, MD, Achille Iolascon, MD, PhD

Blood (2012) 120 (21): 3184.

https://doi.org/10.1182/blood.V120.21.3184.3184

Published: 2012

Journal Articles

In Vitro Characterization of R14W Mutation in SEC23B , the CDAII Causative Gene

Maria Rosaria Esposito, Roberta Russo, Annaelena Troiano, Immacolata Andolfo, Roberta Asci, Achille Iolascon, MD, PhD

Blood (2011) 118 (21): 2098.

https://doi.org/10.1182/blood.V118.21.2098.2098

Published: 2011

Journal Articles

COPII Complex Characterization During Erythroid Differentiation and Its Involvement in CDAII Disease.

Roberta Russo, Maria Rosaria Esposito, Daniela Spano, Luigia De Falco, Roberta Asci, Carmelo Piscopo, Immacolata Andolfo, Achille Iolascon, MD, PhD

Blood (2009) 114 (22): 3009.

https://doi.org/10.1182/blood.V114.22.3009.3009

Published: 2009

NARROW

Evaluating the Clinical Impact of Hemoglobinopathy and Hereditary Red Blood Cell Disorder Co-Inheritance in a Cohort of 315 Patients

pkm2 Binds to the Regulatory Regions of Gata-1 and stat5 in β-Thalassemic Mouse Erythroblasts

Single-Cell Transcriptomic Analysis of Bone Marrow from Humanized Sickle Cell Mice Reveals a Subpopulation of Highly-Expressing S100A8/A9 Mesenchymal Stem Cells

PIEZO1 Gain-of-Function Variants Lead to Alterations in Late-Stage Erythropoiesis By Enhancing Enucleation Rate

Unraveling the Role of PIEZO1 in Stressed Erythropoiesis: Implications for Dyserythropoiesis and Potential Therapeutic Targets in Dehydrated Hereditary Stomatocytosis

Colchicine Protects Against Cardiomyopathy in Humanized Mouse Model for Sickle Cell Disease

Evaluation of the Main Regulators of Systemic Iron Homeostasis in Pyruvate Kinase Deficiency

Nrf2 Plays a Key Role in Iron-Overload Cardiomyopathy

PIEZO1 Mutation May Determine Early Onset of Clinical Manifestation of Anemia of Myelodysplastic Syndromes

Congenital dyserythropoietic anemias

The Novel Role That Nrf2 Plays in Erythropoiesis during Aging

Resolution of sickle cell disease–associated inflammation and tissue damage with 17 R -resolvin D1

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II

Detection of Familial Pseudohyperkalemia Among Italian Blood Donors By Genetic Screening for the R276W Mutation in ABCB6

Erfe-Encoding FAM132B in Congenital Dyserythropoietic Anemia Type II

Dietary ω-3 Fatty Acid Supplementation As a Potential New Therapy for Vasculopathy in Sickle Cell Disease: Proof of Concept in a Transgenic Mouse Model

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1

Missense Mutations in the ABCB6 Transporter Cause Dominant Familial Pseudohyperkalemia

In Vitro Characterization of R14W Mutation in SEC23B , the CDAII Causative Gene

COPII Complex Characterization During Erythroid Differentiation and Its Involvement in CDAII Disease.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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