Page 1 | Search Results | Blood | American Society of Hematology

1-20 of 60

Sort by

Sort Order Select

Journal Articles

Improvement in Red Blood Cell Physiology in Children with Sickle Cell Anemia Receiving Voxelotor

Satheesh Chonat, MD, Earl Fields, Hannah Baratz, Amanda Watt, Mira Pochron, PhD, Sandy Dixon, Margaret Tonda, PharmD, Joshua Lehrer-Graiwer, MD MPhil, FACC, Clark Brown, MD PhD, David R. Archer, PhD

Blood (2019) 134 (Supplement_1): 2281.

https://doi.org/10.1182/blood-2019-129351

Published: 2019

Journal Articles

Evaluation of the Functional Effects of an African American Glucose-6-Phosphate Dehydrogenase (G6PD) Polymorphism (Val68Met) on RBC Hemolytic Propensity and Post-Transfusion Recovery in a Humanized Mouse Model

Ling Wang, MD PhD, Benjamin Zuchelkowski, Derek Sinchar, Minying Yang, Sebastien Gingras, Tamir Kanias, PhD, Janet S Lee, Daniel Kim-Shapiro, Grier Page, PhD BS, MS, Mark T Gladwin, MD

Blood (2019) 134 (Supplement_1): 102.

https://doi.org/10.1182/blood-2019-124926

Published: 2019

Journal Articles

Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic Anemia

Sule Unal, MD, Tekin Aksu, MD, Cagrı Coskun, MD, Fatma Gumruk, MD

Blood (2019) 134 (Supplement_1): 4794.

https://doi.org/10.1182/blood-2019-124272

Published: 2019

Journal Articles

Multi-Modal Mechanisms and Anti-Sickling of Novel Sulfated Non-Anticoagulant Low Molecular Weight Heparin in Sickle Cell Disease

Shaker A Mousa, PhD BPharm, MBA, MSc, Noureldien Hassan Elsayed Darwish, MDPhDBS, Vandhana Muralidharan-Chari, PhD, Mohamed Qari, MD, Chen Qiukan, J Eric Russell, MD, Osheiza Abdulmalik, DVM

Blood (2018) 132 (Supplement 1): 265.

https://doi.org/10.1182/blood-2018-99-115121

Published: 2018

Journal Articles

Evaluation of Phenotype-Genotype Correlation in Two Common PIEZO1 Mutations p.R2456H and p.L2495_E2495dup

Mary Risinger, PhD, Vandy Black, MDMSc, Loan Hsieh, MD, Renee C. Prins, MD, Jill Menell, MD, Mohamad Badawi, MD, Cynthia Rutherford, MD, Karen L. Bride, MD PhD, Omar Niss, MD, Charles T. Quinn, MD, Katie Giger Seu, PhD, Wenying Zhang, MDPhD, Theodosia A. Kalfa, MD PhD

Blood (2018) 132 (Supplement 1): 1040.

https://doi.org/10.1182/blood-2018-99-117299

Published: 2018

Journal Articles

Hepatocyte nuclear factor 1A deficiency causes hemolytic anemia in mice by altering erythrocyte sphingolipid homeostasis

Karin von Wnuck Lipinski, Sarah Weske, Petra Keul, Susann Peters, Hideo A. Baba, Gerd Heusch, Markus H. Gräler, Bodo Levkau

Blood (2017) 130 (25): 2786–2798.

https://doi.org/10.1182/blood-2017-03-774356

Published: 2017

Includes: Supplemental data

Journal Articles

Sepsis Induced Red Cell Dysfunction (SiRD): Physiology and Mechanisms

Xue Lin, MD PhD, Stephen Rogers, PhD, David Timm, MS, d'Alessandro Angelo, PhD, Prakash Jaya, Ernst Melanie, BS, Julie Prior, PhD, Shah Shivam, PhD, Jackie Wu, Julie Reisz, PhD, Allan Doctor, MD

Blood (2017) 130 (Supplement 1): 3469.

https://doi.org/10.1182/blood.V130.Suppl_1.3469.3469

Published: 2017

Journal Articles

Pathophysiologic Implications of Type-2 Phosphatidylserine-Positive Erythrocytes in Hemoglobin SS Disease (sickle cell anemia) and β-Thalassemia

Yamaja Setty, PhD, Suhita Gayen-Betal, PhD, Marie Stuart, MD

Blood (2017) 130 (Supplement 1): 3521.

https://doi.org/10.1182/blood.V130.Suppl_1.3521.3521

Published: 2017

Journal Articles

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

Grier Page, PhD BS, MS, Tamir Kanias, PhD, Marion C. Lanteri, PhD, Yuelong Guo, PhD, Alan E. Mast, MDPhD, Richard G. Cable, MD, Bryan R Spencer, MPH, Joseph Kiss, MD, Stacey Endres, MPH, Donald Brambilla, PhD, Seyed Mehdi Nouraie, PhD MD, Victor R. Gordeuk, MD, Steven Kleinman, MD, Mark T Gladwin, MD, Michael Paul Busch, MD PhD

Blood (2017) 130 (Supplement 1): 1117.

https://doi.org/10.1182/blood.V130.Suppl_1.1117.1117

Published: 2017

Journal Articles

The Flow Cytometric Osmotic Fragility Test Is an Effective Screening Method for Dehydrated Hereditary Stomatocytosis

Taiju Utsugisawa, MD PhD, Takuya Iwasaki, MLS, Takako Aoki, MLS, Yoshio Okamoto, MLS, Takahiro Kawakami, MD PhD, Hiromi Ogura, MD PhD, Hitoshi Kanno, MDPhD

Blood (2017) 130 (Supplement 1): 929.

https://doi.org/10.1182/blood.V130.Suppl_1.929.929

Published: 2017

Journal Articles

Clinical Application of Massively Parallel Sequencing in the Diagnosis of Hereditary Hemolytic and Dyserythropoietic Anemias

Harry Lesmana, MD, Georgios E Christakopoulos, MD, Katie Giger Seu, PhD, Mary Risinger, PhD, Hatice Duzkale, MD MPH, PhD, Neha Dagaonkar, Kejian Zhang, MD, Theodosia A Kalfa, MD PhD

Blood (2016) 128 (22): 4746.

https://doi.org/10.1182/blood.V128.22.4746.4746

Published: 2016

Journal Articles

Contribution of Imaging Flow Cytometry to Storage Lesion Assessment: Identification of a Sub-Population of Morphologically Altered Erythrocytes

Pascal Amireault, Camille A Roussel, Michaël Dussiot, Mickael Marin, Alexandre Morel, Papa Alioune Ndour, Julien Duez, Caroline Le Van Kim, Olivier Hermine, Yves Colin-Aronovicz, Pierre A Buffet

Blood (2015) 126 (23): 2343.

https://doi.org/10.1182/blood.V126.23.2343.2343

Published: 2015

Journal Articles

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

Paola Bianchi, PhD, Elisa Fermo, PhD, Jennifer C Eng, Jacob C Ulirsch, Cristina Vercellati, BSc, Paola Braidotti, MD, Gordon Hildick-Smith, Timothy J Satchwell, PhD, Stephanie Pellegrin, PhD, Alberto Zanella, MD, Wilma Barcellini, MD, Barry H. Paw, MD, PhD, Ashley Mark Toye, PhD, Vijay G Sankaran, MD PhD

Blood (2015) 126 (23): 272.

https://doi.org/10.1182/blood.V126.23.272.272

Published: 2015

Journal Articles

Gardos Channel Mutation Is Associated with Hereditary Dehydrate Stomatocytosis: a Complex Channelopathy

Elisa Fermo, PhD, Anna Yu. Bogdanova, Dr PhD, Polina Petkova-Kirova, PhD, Anna Zaninoni, BSc, PhD, Anna Paola Marcello, PhD, Asya Makhro, PhD, Pascal Hänggi, PhD, Laura Hertz, PhD, Jens Danielczok, Nadia Mirra, MD, Alberto Zanella, MD, Wilma Barcellini, MD, Kaestner Lars, PhD, Paola Bianchi, PhD

Blood (2015) 126 (23): 3333.

https://doi.org/10.1182/blood.V126.23.3333.3333

Published: 2015

Journal Articles

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Satheesh Chonat, MD, Mary Risinger, Neha Dagaonkar, Tamara Maghathe, Jennifer Rothman, MD, Jessica Connor, Karen Kalinyak, MD, Amber H Begtrup, PhD, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 941.

https://doi.org/10.1182/blood.V126.23.941.941

Published: 2015

Journal Articles

Diagnostic Power of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) Evaluated in 118 Patients Affected By Hereditary Hemolytic Anemias

Paola Bianchi, PhD, Anna Zaninoni, BSc, PhD, Elisa Fermo, PhD, Cristina Vercellati, BSc, Marcello Anna Paola, BSc, Alberto Zanella, MD, Agostino Cortelezzi, MD, Wilma Barcellini, MD

Blood (2015) 126 (23): 942.

https://doi.org/10.1182/blood.V126.23.942.942

Published: 2015

Journal Articles

Type-2 Phosphatidylserine (PS)-Positive Erythrocytes and Their Association with Markers of Hemolysis and Hemostatic Activation in Children with Sickle Cell Disease (SCD)

Yamaja B. Setty, PhD, Suhita Gayennebetal, Nigel S. Key, MB, ChB, Marie Stuart, MD

Blood (2015) 126 (23): 943.

https://doi.org/10.1182/blood.V126.23.943.943

Published: 2015

Journal Articles

New Insights in the Potential Effect of Transfusing Red Blood Cells that Have Been Stored for Different Periods

Simone A Glynn, MD, Darrell J Triulzi, MD, John Roback, MD PhD, Harvey G. Klein, MD

Blood (2015) 126 (23): SCI-37.

https://doi.org/10.1182/blood.V126.23.SCI-37.SCI-37

Published: 2015

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

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Hereditary Hemolytic Anemias

Roberto H Nussenzveig, PhD, Nikhil Sangle, MD, Robert D. Christensen, MD, Mohamed E Salama, MD, Josef Prchal, MD, Hassan Yaish, MD, Archana M Agarwal, MD

Blood (2013) 122 (21): 3421.

https://doi.org/10.1182/blood.V122.21.3421.3421

Published: 2013

NARROW

Improvement in Red Blood Cell Physiology in Children with Sickle Cell Anemia Receiving Voxelotor

Evaluation of the Functional Effects of an African American Glucose-6-Phosphate Dehydrogenase (G6PD) Polymorphism (Val68Met) on RBC Hemolytic Propensity and Post-Transfusion Recovery in a Humanized Mouse Model

Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic Anemia

Multi-Modal Mechanisms and Anti-Sickling of Novel Sulfated Non-Anticoagulant Low Molecular Weight Heparin in Sickle Cell Disease

Evaluation of Phenotype-Genotype Correlation in Two Common PIEZO1 Mutations p.R2456H and p.L2495_E2495dup

Hepatocyte nuclear factor 1A deficiency causes hemolytic anemia in mice by altering erythrocyte sphingolipid homeostasis

Sepsis Induced Red Cell Dysfunction (SiRD): Physiology and Mechanisms

Pathophysiologic Implications of Type-2 Phosphatidylserine-Positive Erythrocytes in Hemoglobin SS Disease (sickle cell anemia) and β-Thalassemia

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

The Flow Cytometric Osmotic Fragility Test Is an Effective Screening Method for Dehydrated Hereditary Stomatocytosis

Clinical Application of Massively Parallel Sequencing in the Diagnosis of Hereditary Hemolytic and Dyserythropoietic Anemias

Contribution of Imaging Flow Cytometry to Storage Lesion Assessment: Identification of a Sub-Population of Morphologically Altered Erythrocytes

Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia

Gardos Channel Mutation Is Associated with Hereditary Dehydrate Stomatocytosis: a Complex Channelopathy

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Diagnostic Power of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) Evaluated in 118 Patients Affected By Hereditary Hemolytic Anemias

Type-2 Phosphatidylserine (PS)-Positive Erythrocytes and Their Association with Markers of Hemolysis and Hemostatic Activation in Children with Sickle Cell Disease (SCD)

New Insights in the Potential Effect of Transfusing Red Blood Cells that Have Been Stored for Different Periods

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

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Hereditary Hemolytic Anemias

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only