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Journal Articles

Pediatric Evans Syndrome Displays Broad Immune Dysregulation Characterized By Extra-Follicular B-Cell Responses and Unique Autoantibody Repertoire

Deepak Kumar, Chengyu Prince, Tyler Hulett, Pedro Ramos, Oscar Candelario, Laura Youngblood, Michael Briones, Carolyn Bennett, Shanmuganathan Chandrakasan

Blood (2022) 140 (Supplement 1): 1646–1647.

https://doi.org/10.1182/blood-2022-169527

Published: 2022

Journal Articles

Potential Therapeutic Applications of Jak2 Inhibitors and Hif2a-ASO for the Treatment of β-Thalassemia Intermedia and Major

Carla Casu, Paraskevi Rea Oikonomidou, MD, Vania Lo Presti, Mariam Aghajan, PhD, Shuling Guo, PhD, Abdulmalik Osheiza, Luca Melchiori, Pedro Ramos, Stefano Rivella, PhD

Blood (2016) 128 (22): 1012.

https://doi.org/10.1182/blood.V128.22.1012.1012

Published: 2016

Journal Articles

Macrophages Regulate Stress Erythropoiesis Through Direct Cellular Interactions Associated With Integrin β1-Focal Adhesion Kinase Signaling

Bart J Crielaard, MD, PhD, Carla Casu, PhD, Pedro Ramos, PhD, Sara Gardenghi, PhD, Laura Breda, PhD, Ritama Gupta, Stefano Rivella, PhD

Blood (2013) 122 (21): 307.

https://doi.org/10.1182/blood.V122.21.307.307

Published: 2013

Journal Articles

Removal of Macrophages From the Erythroid Niche Impairs Stress Erythropoiesis but Improves Pathophysiology of Polycythemia Vera and Beta-Thalassemia

Pedro Ramos, PhD, Carla Casu, PhD, Sara Gardenghi, PhD, Laura Breda, Ph.D, Bart J Crielaard, PhD, Ritama Gupta, Undergraduate student, Ella Guy, Maria F Mariongiu, PhD, Ross L. Levine, Omar Abdel-Wahab, PhD, Benjamin L. Ebert, Nico van Rooijen, PhD, Saghi Ghaffari, MD, PhD, Robert W Grady, PhD, Patricia Giardina, MD, Stefano Rivella, PhD

Blood (2012) 120 (21): 81.

https://doi.org/10.1182/blood.V120.21.81.81

Published: 2012

Journal Articles

Decreased hepcidin expression in murine β-thalassemia is associated with suppression of Bmp/Smad signaling

Nermi L. Parrow, Sara Gardenghi, Pedro Ramos, Carla Casu, Robert W. Grady, Erik R. Anderson, Yatrik M. Shah, Huihui Li, Yelena Z. Ginzburg, Robert E. Fleming, Stefano Rivella

Blood (2012) 119 (13): 3187–3189.

https://doi.org/10.1182/blood-2012-01-405563

Published: 2012

Journal Articles

Potential Therapeutic Applications of Jak2 Inhibitors in Beta-Thalassemia and Sickle Cell Disease,

Carla Casu, PhD, Pedro Ramos, PhD, Luca Melchiori, PhD, Ella Guy, Eliezer A. Rachmilewitz, Patricia Giardina, MD, Robert W Grady, PhD, Maria de Sousa, MD, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 3187.

https://doi.org/10.1182/blood.V118.21.3187.3187

Published: 2011

Journal Articles

The Regulation of Hepcidin in β-Thalassemia

Nermi Parrow, PhD, Sara Gardenghi, PhD, Pedro Ramos, PhD, Yatrik Shah, PhD, Robert Fleming, MD, Carla Casu, PhD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 901.

https://doi.org/10.1182/blood.V118.21.901.901

Published: 2011

Journal Articles

Macrophages Impair Erythroid Development in β-Thalassemia Intermedia

Carla Casu, PhD, Pedro Ramos, PhD, Ella Guy, Nico van Rooijen, PhD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 1035.

https://doi.org/10.1182/blood.V118.21.1035.1035

Published: 2011

Journal Articles

Investigating the Role of Cytokines and Hepcidin in Anemia of Inflammation

Sara Gardenghi, PhD, Thomas M. Renaud, MD, Alessandra Meloni, PhD, Pedro Ramos, PhD, Carla Casu, PhD, Keegan S Cooke, Barbra J Sasu, PhD, Patricia Giardina, MD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 1046.

https://doi.org/10.1182/blood.V118.21.1046.1046

Published: 2011

Journal Articles

Enhanced erythropoiesis in Hfe -KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis

Pedro Ramos, Ella Guy, Nan Chen, Catia C. Proenca, Sara Gardenghi, Carla Casu, Antonia Follenzi, Nico Van Rooijen, Robert W. Grady, Maria de Sousa, Stefano Rivella

Blood (2011) 117 (4): 1379–1389.

https://doi.org/10.1182/blood-2010-09-307462

Published: 2011

Includes: Supplemental data

Journal Articles

ß-Thalassemic Mice Require Functional Hfe to Modulate Hepcidin Expression In Response to Iron Overload

Pedro Ramos, Sara Gardenghi, PhD, Robert W Grady, PhD, Maria de Sousa, MD, PhD, Stefano Rivella, PhD

Blood (2010) 116 (21): 2063.

https://doi.org/10.1182/blood.V116.21.2063.2063

Published: 2010

Journal Articles

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

Sara Gardenghi, PhD, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Xiuli An, MD, PhD, Mohandas Narla, DSc, Yelena Ginzburg, MD, Eliezer A. Rachmilewitz, MD, Patricia Giardina, MD, Robert W Grady, Stefano Rivella, PhD

Blood (2010) 116 (21): 1009.

https://doi.org/10.1182/blood.V116.21.1009.1009

Published: 2010

Journal Articles

Hfe Modulates the Response to Erythopoietic Stress In Wt Mice by Two Distinct Mechanisms

Pedro Ramos, PhD, Ella Guy, Robert W Grady, PhD, Maria de Sousa, MD, PhD, Stefano Rivella, PhD

Blood (2010) 116 (21): 4251.

https://doi.org/10.1182/blood.V116.21.4251.4251

Published: 2010

Journal Articles

Absence of the Hemochromatosis Gene Hfe Confers Protection Under Conditions of Stress Erythropoiesis.

Pedro Ramos, Ella Guy, Nan Chen, Sara Gardenghi, Robert W. Grady, PhD, Maria De Sousa, MD, Stefano Rivella, PhD

Blood (2009) 114 (22): 4044.

https://doi.org/10.1182/blood.V114.22.4044.4044

Published: 2009

Journal Articles

Macrophage Depletion Leads to Modification of Thalassemic Phenotype.

Pedro Ramos, Ella Guy, Nan Chen, Robert W. Grady, PhD, Barry S. Coller, MD, Maria De Sousa, MD, Stefano Rivella, PhD

Blood (2009) 114 (22): 2023.

https://doi.org/10.1182/blood.V114.22.2023.2023

Published: 2009

Journal Articles

Hepcidin: A Clue for a New Role for Lymphocytes.

Jorge P Pinto, PhD, Vera Dias, Heinz Zoller, MD, Pedro N Rodrigues, PhD, Helena Carmo, Pedro Ramos, Félix Carvalho, PhD, Graça Porto, MD, PhD, Maria de Sousa, MD, PhD

Blood (2009) 114 (22): 1999.

https://doi.org/10.1182/blood.V114.22.1999.1999

Published: 2009

Journal Articles

Absence of the Hemochromatosis Gene HFE Confers Protection Under Conditions of Stress Erythropoiesis.

Pedro Ramos, Ella Guy, Laura Breda, PhD, Sara Gardenghi, PhD, Robert W Grady, Ph.D, Maria De Sousa, MD, Stefano Rivella, PhD

Blood (2008) 112 (11): 3848.

https://doi.org/10.1182/blood.V112.11.3848.3848

Published: 2008

Journal Articles

Increased Hepcidin Expression in Mice Affected by β-Thalassemia Reduces Iron Overload with No Effect on Anemia

Sara Gardenghi, PhD, Maria Franca Marongiu, Kristen Muirhead, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Antonia Follenzi, Eliezer Rachmilewitz, M.D, Patricia Giardina, MD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2008) 112 (11): 128.

https://doi.org/10.1182/blood.V112.11.128.128

Published: 2008

Journal Articles

Potential Use of Jak2 Inhibitors to Limit Ineffective Erythropoiesis and Reverse Splenomegaly in β-Thalassemia.

Luca Melchiori, Ella Guy, Ilaria Libani, Ph.D, Raffaella Schirò, MD, Ph.D, Pedro Ramos, Laura Breda, Ph.D, Amy Chadburn, MD, Yi-Fang Liu, Maria De Sousa, MD, Eliezer Rachmilewitz, M.D, Patricia J Giardina, MD, Robert W Grady, Ph.D, Stefano Rivella, Ph.D

Blood (2008) 112 (11): 1877.

https://doi.org/10.1182/blood.V112.11.1877.1877

Published: 2008

Journal Articles

Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia

Blood (2008) 112 (3): 875–885.

https://doi.org/10.1182/blood-2007-12-126938

Published: 2008

Includes: Supplemental data

NARROW

Pediatric Evans Syndrome Displays Broad Immune Dysregulation Characterized By Extra-Follicular B-Cell Responses and Unique Autoantibody Repertoire

Potential Therapeutic Applications of Jak2 Inhibitors and Hif2a-ASO for the Treatment of β-Thalassemia Intermedia and Major

Macrophages Regulate Stress Erythropoiesis Through Direct Cellular Interactions Associated With Integrin β1-Focal Adhesion Kinase Signaling

Removal of Macrophages From the Erythroid Niche Impairs Stress Erythropoiesis but Improves Pathophysiology of Polycythemia Vera and Beta-Thalassemia

Decreased hepcidin expression in murine β-thalassemia is associated with suppression of Bmp/Smad signaling

Potential Therapeutic Applications of Jak2 Inhibitors in Beta-Thalassemia and Sickle Cell Disease,

The Regulation of Hepcidin in β-Thalassemia

Macrophages Impair Erythroid Development in β-Thalassemia Intermedia

Investigating the Role of Cytokines and Hepcidin in Anemia of Inflammation

Enhanced erythropoiesis in Hfe -KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis

ß-Thalassemic Mice Require Functional Hfe to Modulate Hepcidin Expression In Response to Iron Overload

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

Hfe Modulates the Response to Erythopoietic Stress In Wt Mice by Two Distinct Mechanisms

Absence of the Hemochromatosis Gene Hfe Confers Protection Under Conditions of Stress Erythropoiesis.

Macrophage Depletion Leads to Modification of Thalassemic Phenotype.

Hepcidin: A Clue for a New Role for Lymphocytes.

Absence of the Hemochromatosis Gene HFE Confers Protection Under Conditions of Stress Erythropoiesis.

Increased Hepcidin Expression in Mice Affected by β-Thalassemia Reduces Iron Overload with No Effect on Anemia

Potential Use of Jak2 Inhibitors to Limit Ineffective Erythropoiesis and Reverse Splenomegaly in β-Thalassemia.

Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia

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American Society of Hematology

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ASH Publications

American Society of Hematology

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