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Journal Articles

Development of a Personalized 3D Carotid Model for Cerebral Vasculopathy Monitoring in Sickle Cell Disease

Nguyen-Peyre Kim-Anh, PhD, Laurène Lenoir, Valentin Amar, Frédéric Segonds, Nuriye Akçay, Seguin Marion, Philippe Connes, PhD, France Pirenne, MD PhD, Jean-Frédéric Gerbeau, Irène Vignon-Clémentel, Suzanne Verlhac, MD, Pablo Bartolucci, MD PhD

Blood (2019) 134 (Supplement_1): 3570.

https://doi.org/10.1182/blood-2019-124327

Published: 2019

Journal Articles

Iron Restriction Improves Markers of Disease Severity in the Townes Mouse Model of Sickle Cell Anemia

Nermi Parrow, PhD, Pierre-Christian Violet, PhD, Nisha George, PhD, Faris Ali, Shivam Bhanvadia, Mark Levine, MD, Robert E Fleming, MD

Blood (2019) 134 (Supplement_1): 2261.

https://doi.org/10.1182/blood-2019-130732

Published: 2019

Journal Articles

Genetic Engineering in Hematopoietic Stem Cells for Gene Therapy of Hemoglobinopathies

Giuliana Ferrari, PhD

Blood (2019) 134 (Supplement_1): SCI-23.

https://doi.org/10.1182/blood-2019-121119

Published: 2019

Journal Articles

Burden of Illness of Sickle Cell Disease in Countries of the Middle East: A Systematic Literature Review

Miranda Bailey, Megan Gibbs, Nidhi Dani, Ari Mendell, Melissa Thompson

Blood (2019) 134 (Supplement_1): 5867.

https://doi.org/10.1182/blood-2019-131699

Published: 2019

Journal Articles

A Single -195 C < G HBG1 Promoter Mediated By CRISPR/Cas9 Genome Editing Induces Fetal Hemoglobin Synthesis in Hudep-2

Priscila Keiko Matsumoto Martin, PhD, Dulcinéia Martins de Albuquerque, PhD, Carolina Lanaro, PhD, Ryo Kurita, PhD, Yukio Nakamura, MD PhD, Fernando F. Costa, MD, PhD

Blood (2018) 132 (Supplement 1): 3481.

https://doi.org/10.1182/blood-2018-99-118534

Published: 2018

Journal Articles

New Insights into F-Cells, F-Reticulocytes and the Role of Fetal Hemoglobin in Protecting Sickle Red Cells from Hemolysis upon Mechanical Stress

Sara El Hoss, Maria Alejandra Lizarralde Iragorri, Valentine Brousse, MD, Michaël Dussiot, PhD, Sophie Lefevre, PhD, Alexander Rodrigo Ferreira, Yann Lamarre, PhD, Ana Cristina Silva Pinto, MD PhD, Simone Kashima, PhD, Claudine Lapoumeroulie, PhD, Dimas Tadeu Covas, MD PhD, Caroline Le Van Kim, PhD, Yves Colin Aronovicz, PhD, Jacques Elion, MD PhD, Olivier Français, PhD, Bruno Le Pioufle, PhD, Wassim El Nemer, PhD

Blood (2017) 130 (Supplement 1): 3513.

https://doi.org/10.1182/blood.V130.Suppl_1.3513.3513

Published: 2017

Journal Articles

Recovery of Thymic Function after Allogeneic Hematopoietic Stem Cell Transplantation in with Sickle Cell Anemia Patients

Luciana Ribeiro Jarduli, BPharm, MMSc, Emmanuel Clave, PhD, Isabelle Fournier, Dimas Tadeu Covas, MD PhD, Ana Cristina Silva Pinto, MD PhD, Belinda Pinto Simões, MD PhD, Antoine Toubert, MD PhD, Kelen Cristina Ribeiro Malmegrim de Farias, PhD

Blood (2017) 130 (Supplement 1): 3261.

https://doi.org/10.1182/blood.V130.Suppl_1.3261.3261

Published: 2017

Journal Articles

Monoclonal Gammopathies: Electronic Subspecialty Consultation

Nicholas Burwick, MD, Jacob Stein, David A Garcia, MD, Virginia C. Broudy, MD, Robert E. Richard, MD PhD

Blood (2017) 130 (Supplement 1): 673.

https://doi.org/10.1182/blood.V130.Suppl_1.673.673

Published: 2017

Journal Articles

Microcytic Anemia and Celiac Disease Preceding Pulmonary Symptoms in Lane-Hamilton Syndrome

Robert Szulawski, DO, Catherine D Quinn, MD, Eric Safyan, MD

Blood (2017) 130 (Supplement 1): 4753.

https://doi.org/10.1182/blood.V130.Suppl_1.4753.4753

Published: 2017

Journal Articles

T Cell Repertoire Diversity of Sickle Cell Anemia Patients Treated with Allogeneic Hematopoietic Stem Cell Transplantation and Conventional Treatments

Luciana Ribeiro Jarduli, BPharm, MSc, PhD Student, Adriana Aparecida Marques, BS, Julia Teixeira Cottas de Azevedo, MSc, Keli Cristina de Lima, BS, Wilson Araújo da Silva Júnior, PhD, Dimas Tadeu Covas, MD, PhD, Belinda Pinto Simoes, MD, PhD, Ana Cristina Silva Pinto, MD, PhD, Kelen Cristina Ribeiro Malmegrim de Farias, BPharm, PhD

Blood (2016) 128 (22): 4586.

https://doi.org/10.1182/blood.V128.22.4586.4586

Published: 2016

Journal Articles

Red Cell Transport Abnormalities As Predictors of the Development of Renal Disease in Children with Sickle Cell Disease

Sanjay Tewari, MBBS, MRCPCH, John Gibson, Stephan Menzel, PhD, Anke Hannemann, Swee Lay Thein, MD, Bukola T Gbotosho, Halima W M Al Balushi, David C Rees, MA, FRCP

Blood (2016) 128 (22): 1317.

https://doi.org/10.1182/blood.V128.22.1317.1317

Published: 2016

Journal Articles

Examining the Clinical Features and Underlying Cardiovascular Risk Among Patients with Polycythemia Vera in the REVEAL Study

Brady L. Stein, MD, Ahmad Naim, MD, Michael R. Grunwald, MD, Alison R. Moliterno, MD, Stephen T. Oh, MD PhD, Dilan Paranagama, PhD, Joseph A. Cordaro, PharmD, MBA, Hao Sun, MS, Shreekant Parasuraman, BPharm, PhD, Ralph V. Boccia, Ruben Mesa, MD FACP

Blood (2016) 128 (22): 1934.

https://doi.org/10.1182/blood.V128.22.1934.1934

Published: 2016

Journal Articles

The Endothelin Receptor Etb Plays a Crucial Role for Recruitment of Neutrophils to the Vascular Wall in Sickle Cell Disease

Bérengere Koehl, MD, Pierre Nivoit, PhD, Wassim El Nemer, PhD, Catia Pereira, Valentine Brousse, MD, Lea Guyonnet, Anna Chipont, Olivia Lenoir, Malika Benkerrou, MD, Yves Colin Aronovicz, PhD, Pierre-Louis Tharaux, Caroline Le Van Kim, PhD

Blood (2016) 128 (22): 857.

https://doi.org/10.1182/blood.V128.22.857.857

Published: 2016

Journal Articles

Singer K, Fisher B. Studies on abnormal hemoglobins, VI: electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon. Blood . 1953;8(3): 270-275 .

Blood (2016) 127 (7): 791.

https://doi.org/10.1182/blood-2015-12-688135

Published: 2016

Journal Articles

Accuracy of a Rapid and Simple Point-of-Care Test for Sickle Cell Disease

Patrick T. McGann, MD MS, Beverly A. Schaefer, MD, Mary C. Paniagua, MA, Thad A. Howard, MS, Russell E. Ware, MD PhD

Blood (2015) 126 (23): 2182.

https://doi.org/10.1182/blood.V126.23.2182.2182

Published: 2015

Journal Articles

Investigation of Two Combination HbF Induction Regimens, RN-1 and Hydroxyurea Versus RN-1 and Decitabine, in a Humanized Sickle Cell Mouse Model

Ramasamy Jagadeeswaran, PhD, Yash Agarwal, Vinzon Ibanez, Maria Armila Ruiz, Kestis Vaitkus, Joseph DeSimone, PhD, Donald Lavelle, PhD, Angela Rivers, MD PhD

Blood (2015) 126 (23): 3386.

https://doi.org/10.1182/blood.V126.23.3386.3386

Published: 2015

Journal Articles

Desaturation Is Related to the Presence of Dense Red Blood Cells in Sickle Cell Patients and Is Reversed By Hydroxyurea

Gaetana Di Liberto, Laurent Kiger, Michael Marden, Laurent Boyer, Marc Conti, Anoosha Habibi, Marie Georgine Rakotoson, Sanam Khorgami, Benoit Vingert, Bernard Maitre, Frédéric Galacteros, France Noizat-Pirenne, Pablo Bartolucci

Blood (2014) 124 (21): 2713.

https://doi.org/10.1182/blood.V124.21.2713.2713

Published: 2014

Journal Articles

Comparing Strategies to Reactivate Fetal Globin Expression for the Treatment of Beta-Globinopathies

Laura Breda, PhD, Jeremy W. Rupon, MD PhD, Irene Motta, MD, Wulan Deng, Gerd A. Blobel, MD PhD, Stefano Rivella, PhD

Blood (2014) 124 (21): 333.

https://doi.org/10.1182/blood.V124.21.333.333

Published: 2014

Journal Articles

Peripheral Blood As a Source Of Cells For Regenerative Medicine Applications In Sickle Cell Disease

Atsushi Fujita, MD, PhD, Courtney D. Fitzhugh, MD, Matthew M. Hsieh, MD, John F. Tisdale, MD, Naoya Uchida, MD, PhD

Blood (2013) 122 (21): 2209.

https://doi.org/10.1182/blood.V122.21.2209.2209

Published: 2013

Journal Articles

Hemoglobin Variants That Produce Abnormal Elevations In Hb A 1c In The Clinical Laboratory: Electrophoretic Patterns, HPLC Analysis and Globin Gene Sequencing

Neil S. Harris, M.D., David H.K. Chui, MD

Blood (2013) 122 (21): 4695.

https://doi.org/10.1182/blood.V122.21.4695.4695

Published: 2013

NARROW

Development of a Personalized 3D Carotid Model for Cerebral Vasculopathy Monitoring in Sickle Cell Disease

Iron Restriction Improves Markers of Disease Severity in the Townes Mouse Model of Sickle Cell Anemia

Genetic Engineering in Hematopoietic Stem Cells for Gene Therapy of Hemoglobinopathies

Burden of Illness of Sickle Cell Disease in Countries of the Middle East: A Systematic Literature Review

A Single -195 C < G HBG1 Promoter Mediated By CRISPR/Cas9 Genome Editing Induces Fetal Hemoglobin Synthesis in Hudep-2

New Insights into F-Cells, F-Reticulocytes and the Role of Fetal Hemoglobin in Protecting Sickle Red Cells from Hemolysis upon Mechanical Stress

Recovery of Thymic Function after Allogeneic Hematopoietic Stem Cell Transplantation in with Sickle Cell Anemia Patients

Monoclonal Gammopathies: Electronic Subspecialty Consultation

Microcytic Anemia and Celiac Disease Preceding Pulmonary Symptoms in Lane-Hamilton Syndrome

T Cell Repertoire Diversity of Sickle Cell Anemia Patients Treated with Allogeneic Hematopoietic Stem Cell Transplantation and Conventional Treatments

Red Cell Transport Abnormalities As Predictors of the Development of Renal Disease in Children with Sickle Cell Disease

Examining the Clinical Features and Underlying Cardiovascular Risk Among Patients with Polycythemia Vera in the REVEAL Study

The Endothelin Receptor Etb Plays a Crucial Role for Recruitment of Neutrophils to the Vascular Wall in Sickle Cell Disease

Singer K, Fisher B. Studies on abnormal hemoglobins, VI: electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon. Blood . 1953;8(3): 270-275 .

Accuracy of a Rapid and Simple Point-of-Care Test for Sickle Cell Disease

Investigation of Two Combination HbF Induction Regimens, RN-1 and Hydroxyurea Versus RN-1 and Decitabine, in a Humanized Sickle Cell Mouse Model

Desaturation Is Related to the Presence of Dense Red Blood Cells in Sickle Cell Patients and Is Reversed By Hydroxyurea

Comparing Strategies to Reactivate Fetal Globin Expression for the Treatment of Beta-Globinopathies

Peripheral Blood As a Source Of Cells For Regenerative Medicine Applications In Sickle Cell Disease

Hemoglobin Variants That Produce Abnormal Elevations In Hb A 1c In The Clinical Laboratory: Electrophoretic Patterns, HPLC Analysis and Globin Gene Sequencing

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American Society of Hematology

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ASH Publications

American Society of Hematology

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