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Journal Articles

A Phase 2 Open-Label Study of Danicopan (ACH-0144471) in Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Have an Inadequate Response to Eculizumab Monotherapy

Austin Kulasekararaj, MBBS MDMRCP FRCPath, Antonio M. Risitano, MD PhD, Jaroslaw P. Maciejewski, MD PhD, Rosario Notaro, MD, Peter Browett, BMedSci, MBChB, FRACP, FRCPA, Jong-Wook Lee, MD, Mingjun Huang, PhD, Michael Geffner, MD, Robert A. Brodsky, MD

Blood (2019) 134 (Supplement_1): 3514.

https://doi.org/10.1182/blood-2019-124748

Published: 2019

Journal Articles

Mechanistic Evaluation of Efficacy Using Biomarkers of the Oral, Small Molecule Factor D Inhibitor, Danicopan (ACH-4471), in Untreated Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH)

Antonio M. Risitano, MD PhD, Jong Wook Lee, MD PhD, Rosario Notaro, MD, Robert A. Brodsky, MD, Austin Kulasekararaj, MBBS MDMRCP FRCPath, Jaroslaw P. Maciejewski, MD PhD, Mingjun Huang, PhD, Michael Geffner, MD, Peter Browett, BMedSci, MBChB, FRACP, FRCPA

Blood (2019) 134 (Supplement_1): 2226.

https://doi.org/10.1182/blood-2019-124837

Published: 2019

Journal Articles

Red Blood Cell Adhesion Is Increased in the Young Adult Population with Sickle Cell Disease

Erina Quinn, BA, Charlotte Yuan, BA, Sargam Kapoor, MD, Karen Ireland, RN, Janine Keenan, RN, Deepa Manwani, MD, Umut A. Gurkan, PhD, Jane Little, MD

Blood (2018) 132 (Supplement 1): 2387.

https://doi.org/10.1182/blood-2018-99-120175

Published: 2018

Journal Articles

KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Deborah Rund, MD, Dvora Filon, PhD, Natalie Bloch Isenberg, MD, Neta Goldschmidt, MD

Blood (2018) 132 (Supplement 1): 3640.

https://doi.org/10.1182/blood-2018-99-113903

Published: 2018

Journal Articles

Evaluation of Clinical and Morphological Practices in the Diagnosis of Transplant-Associated Microangiopathy: A Study on Behalf of the Complications and Quality of Life Working Party of the EBMT

Blood (2017) 130 (Supplement 1): 1958.

https://doi.org/10.1182/blood.V130.Suppl_1.1958.1958

Published: 2017

Journal Articles

Lethal and Sub-Lethal Irradiation of Sprague-Dawley Rats Causes Development of Dense Red Blood Cells

Janice Zawaski, PhD, Alireza Paikari, MD, Celeste K Kanne, BA, Omaima Sabek, PhD, M Waleed Gaber, PhD, Vivien Sheehan, MD PhD

Blood (2017) 130 (Supplement 1): 4738.

https://doi.org/10.1182/blood.V130.Suppl_1.4738.4738

Published: 2017

Journal Articles

Pre-Treatment Steady-State Rheology Predicts Response to Hydroxyurea in Patients with Sickle Cell Disease

Alessandro Baldan, PhD, Carly Ginter Summerall, MS, Loretta James, AA, Bogdan R. Dinu, MD, Jonathan M. Flanagan, PhD, Vivien A. Sheehan, MD PhD

Blood (2016) 128 (22): 3661.

https://doi.org/10.1182/blood.V128.22.3661.3661

Published: 2016

Journal Articles

Therapeutic Amelioration of Vaso-Occlusion and Blood Flow Impairment in Transgenic Sickle Mice By the Antioxidant Flavonoid Quercetin

Sangeetha Thangaswamy, PhD, Henny H Billett, MD, Craig A. Branch, PhD, Sandra M. Suzuka, M.S., Seetharama A Acharya, PhD

Blood (2014) 124 (21): 4054.

https://doi.org/10.1182/blood.V124.21.4054.4054

Published: 2014

Journal Articles

Procoagulant Phospholipid Activity, Whole Blood Thromboelastography and Thrombin Generation Assay to Detect Hypercoagulability in Thalassemic Children

Burcak Tatli Gunes, MD, Meral Turker, MD, Salih Gozmen, MD, Yesim Oymak, MD, Yilmaz Ay, MD, Dilek Ince, MD, Gulcihan Ozek, MD, Tuba Hilkay Karapinar, MD, Berna Atabay, MD, Canan Vergin, MD

Blood (2014) 124 (21): 4896.

https://doi.org/10.1182/blood.V124.21.4896.4896

Published: 2014

Journal Articles

Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Robert A. Sokolic, MD, Satheesh Chonat, MD, Mary Risinger, RN, Michael Eckhaus, DVM, Elizabeth Garabedian, RN, MSLS, Katherine R. Calvo, MD, PhD, Irina Maric, MD, Theodosia A. Kalfa, MD PhD, Fabio Candotti, MD

Blood (2014) 124 (21): 1338.

https://doi.org/10.1182/blood.V124.21.1338.1338

Published: 2014

Journal Articles

Hydroxyurea Improves Oxygen Transport Effectiveness in Sickle Cell Anemia Patients

Vivien A. Sheehan, MD PhD, Sheryl Nelson, MPH, Caroline Yappan, Bogdan R. Dinu, MD, Danielle Guffey, MS, Charles G. Minard, PhD, Russell E. Ware, MD, PhD

Blood (2014) 124 (21): 2716.

https://doi.org/10.1182/blood.V124.21.2716.2716

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

Stage Selective Requirement For The N-Terminus Of GATA1 During Erythropoiesis

Monika J Stankiewicz, PhD, Timothy M Chlon, John D Crispino, PhD

Blood (2013) 122 (21): 3670.

https://doi.org/10.1182/blood.V122.21.3670.3670

Published: 2013

Journal Articles

Genetic and Epigenetic Regulation of the Gamma Globin Locus Is Associated with Fetal Hemoglobin Levels and Frequency of Pain in Sickle Cell Disease

Blair Anderson, Ebenezer Enchia, Karen Soldano, B.S., Melanie Garrett, MS, Jude Jonassaint, RN, Laura M. De Castro, MD, Marilyn J. Telen, MD, Allison E Ashley-Koch, PhD

Blood (2012) 120 (21): 3230.

https://doi.org/10.1182/blood.V120.21.3230.3230

Published: 2012

Journal Articles

Abnormal Red Cell Deformability and Aggregation in Sickle Cell Trait

Jon Detterich, MD, Adam M Bush, BS, Roberta Miyeko Kato, MD, Rose Wenby, BS, Thomas D. Coates, MD, Herbert Meiselman, ScD, John C Wood, MD, Ph.D

Blood (2012) 120 (21): 1001.

https://doi.org/10.1182/blood.V120.21.1001.1001

Published: 2012

Journal Articles

Macrothrombocytopenia and Hemolysis Associated with Phytosterolemia

Gaifeng Wang, Zhaoyue Wang, Lijuan Cao, Minghua Jiang, Xia Bai, Changgeng Ruan, MD, PhD

Blood (2010) 116 (21): 2515.

https://doi.org/10.1182/blood.V116.21.2515.2515

Published: 2010

Journal Articles

A Novel Approach for In Vivo Measurement of Red Cell Redox Status

Xiuling Xu, PhD, Katharina von Loehneysen, PhD, Deborah Noack, Andrew Vu, Jeff S. Friedman, MD, PhD

Blood (2010) 116 (21): 2036.

https://doi.org/10.1182/blood.V116.21.2036.2036

Published: 2010

Journal Articles

Jak2 Plays a Critical and Non-Redundant Role In Hematopoiesis throughout Pre- and Post-Natal Life

Sung Park, Ph.D., Kavitha Gnanasambandan, Peter P. Sayeski, Ph.D.

Blood (2010) 116 (21): 2238.

https://doi.org/10.1182/blood.V116.21.2238.2238

Published: 2010

Journal Articles

Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.

Serge Pissard, Corinne Vasseur, Fabienne Toutain, Muriel Silva, Emmanuelle Faubert-Laugé, Elisa Domingues, Michael Marden, Henri Wajcman, Véronique Baudin-Creuza

Blood (2009) 114 (22): 462.

https://doi.org/10.1182/blood.V114.22.462.462

Published: 2009

Journal Articles

GATA-2 and GATA-6 Involvement in Hydroxycarbamide Action On Endothelial Cells in Sickle Cell Disease.

Pauline Lansiaux, Sandrine Laurance, Michelle Hauchecorne, Emmanuelle Verger, Jacques Elion, Claudine Lapouméroulie

Blood (2009) 114 (22): 818.

https://doi.org/10.1182/blood.V114.22.818.818

Published: 2009

NARROW

A Phase 2 Open-Label Study of Danicopan (ACH-0144471) in Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Have an Inadequate Response to Eculizumab Monotherapy

Mechanistic Evaluation of Efficacy Using Biomarkers of the Oral, Small Molecule Factor D Inhibitor, Danicopan (ACH-4471), in Untreated Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH)

Red Blood Cell Adhesion Is Increased in the Young Adult Population with Sickle Cell Disease

KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Evaluation of Clinical and Morphological Practices in the Diagnosis of Transplant-Associated Microangiopathy: A Study on Behalf of the Complications and Quality of Life Working Party of the EBMT

Lethal and Sub-Lethal Irradiation of Sprague-Dawley Rats Causes Development of Dense Red Blood Cells

Pre-Treatment Steady-State Rheology Predicts Response to Hydroxyurea in Patients with Sickle Cell Disease

Therapeutic Amelioration of Vaso-Occlusion and Blood Flow Impairment in Transgenic Sickle Mice By the Antioxidant Flavonoid Quercetin

Procoagulant Phospholipid Activity, Whole Blood Thromboelastography and Thrombin Generation Assay to Detect Hypercoagulability in Thalassemic Children

Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Hydroxyurea Improves Oxygen Transport Effectiveness in Sickle Cell Anemia Patients

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

Stage Selective Requirement For The N-Terminus Of GATA1 During Erythropoiesis

Genetic and Epigenetic Regulation of the Gamma Globin Locus Is Associated with Fetal Hemoglobin Levels and Frequency of Pain in Sickle Cell Disease

Abnormal Red Cell Deformability and Aggregation in Sickle Cell Trait

Macrothrombocytopenia and Hemolysis Associated with Phytosterolemia

A Novel Approach for In Vivo Measurement of Red Cell Redox Status

Jak2 Plays a Critical and Non-Redundant Role In Hematopoiesis throughout Pre- and Post-Natal Life

Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.

GATA-2 and GATA-6 Involvement in Hydroxycarbamide Action On Endothelial Cells in Sickle Cell Disease.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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