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Journal Articles

Management of pyruvate kinase deficiency in children and adults

Rachael F. Grace, Wilma Barcellini

Blood (2020) 136 (11): 1241–1249.

https://doi.org/10.1182/blood.2019000945

Published: 2020

Journal Articles

Relationship between Vaso-Occlusive Crises and Important Complications in Sickle Cell Disease Patients

Miranda Bailey, Ajibola Abioye, George Morgan, Tom Burke, MSc, Tim Disher, Stephen Brown, Ashley Bonner, Eleonore Herquelot, Ludovic Lamarsalle, Fanny Raguideau

Blood (2019) 134 (Supplement_1): 2167.

https://doi.org/10.1182/blood-2019-131721

Published: 2019

Journal Articles

Symptomatic Bilirubin Gallstones in Patients with PNH Treated with Eculizumab

David J. Araten, MD, H. Leon Pachter, Robert J Dring, Elliot Newman, Steven M Cohen

Blood (2019) 134 (Supplement_1): 4795.

https://doi.org/10.1182/blood-2019-124571

Published: 2019

Journal Articles

Economic Burden of End Organ Damage Among Patients with Sickle Cell Disease in the US

Xue Song, Andrew D. Campbell, MD, Ze Cong, PhD, Irene Agodoa, MD, Diane Martinez, DrPH, MPH, Carolyn R. Lew, PhD, Danae Black, Helen Varker, Chris Chan, Sophie M. Lanzkron, MD

Blood (2019) 134 (Supplement_1): 3388.

https://doi.org/10.1182/blood-2019-127173

Published: 2019

Journal Articles

Unusually High Prevalence of Silent Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease

Bindu K Sathi, MD, Yoshida Yilin, PhD, Michael Raymond Weaver, BA, Lila Wahidi Nolan, MD, Barbara Gruner, MD, Cara Hirner, RN, BSN, Vinod V. Balasa, MBBS, Talissa Altes, MD, Carlos Leiva Salinas, MD

Blood (2019) 134 (Supplement_1): 2276.

https://doi.org/10.1182/blood-2019-122975

Published: 2019

Journal Articles

Evaluation of Endocrine Complications in Beta-Thalassemia Intermedia Patients: A Cross Sectional Multi-Center Study

Blood (2018) 132 (Supplement 1): 2343.

https://doi.org/10.1182/blood-2018-99-110903

Published: 2018

Journal Articles

Clinical-Pathological Features of Non-Transfusion Dependent Thalassemia in Adults — a Single Center Study in Hong Kong

Ka Lok Luke Chan, MBBS, MPH, MRCP, Vivien W M Mak, Kate F S Leung, Joyce H Y Kwong, Nelson C N Chan, Kelvin C K Cheng, Natalie P H Chan, Daniel H F Fong, Stephen C C Choy, Carmen K M Ng, Johnny K F Ma, Michael L G Wong, Margaret Ng, Harold K K Lee

Blood (2018) 132 (Supplement 1): 4900.

https://doi.org/10.1182/blood-2018-99-113487

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

Hemolytic, Vaso-Occlusive and Renal Complications of SCD: Report from the Central Missouri Cohort

Lila Wahidi Nolan, MD, Yilin Yoshida, PhD, Emily Coberly, MD, Bindu Kanathezhath Sathi, MD

Blood (2018) 132 (Supplement 1): 1091.

https://doi.org/10.1182/blood-2018-99-113723

Published: 2018

Journal Articles

Function and dysfunction

Narla Mohandas

Blood (2018) 131 (20): 2179–2180.

https://doi.org/10.1182/blood-2018-04-840827

Published: 2018

Journal Articles

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Blood (2018) 131 (20): 2183–2192.

https://doi.org/10.1182/blood-2017-10-810796

Published: 2018

Includes: Supplemental data

Journal Articles

An Urgent Need for Improving Thalassemia Care in Adult Patients Due to a Wide Gap on Current Real-Life Practice and Recommended Clinical Practice Guidelines

Supachai Ekwattanakit, BSc, PhD MD, Chattree Hantaweepant, MD, Archrob Khuhapinant, MD PhD, Noppadol Siritanaratkul, MD, Vip Viprakasit, MD DPhil

Blood (2017) 130 (Supplement 1): 952.

https://doi.org/10.1182/blood.V130.Suppl_1.952.952

Published: 2017

Journal Articles

Detection of Gene Mutations in Patients with Clinically Suspected Heritary Spherocytosis By Next Generation Sequencing

Li Qin, PhD, Yujiao Jia, MD, Donglei Zhang, PhD, Kun Ru, MD PhD

Blood (2017) 130 (Supplement 1): 4740.

https://doi.org/10.1182/blood.V130.Suppl_1.4740.4740

Published: 2017

Journal Articles

Molecular Mechanism of Intrahepatic Cholestasis in Sickle Cell Disease

Tirthadipa Pradhan, PhD, Prithu Sundd, Egemen Tutuncuoglu, MSc

Blood (2017) 130 (Supplement 1): 4775.

https://doi.org/10.1182/blood.V130.Suppl_1.4775.4775

Published: 2017

Journal Articles

Effects of UGT1A1 Polymorphism, Glucose-6-Phosphate Dehydrogenase Deficiency and Deletional (-3.7кb) α-Thalassemia Among Young Nigerians with Sickle Cell Anemia

Oladele Olatunya, MD, Dulcinéia Martins de Albuquerque, Daniela Pinheiro Leonardo, BS, MSc, Kleber Yotsumoto Fertrin, MD PhD, Adekunle Adekile, MBBS, PhD FMCPaed, FWACP, FRCPCH, FRCP, Fernando Ferreira Costa, MD PhD

Blood (2017) 130 (Supplement 1): 2242.

https://doi.org/10.1182/blood.V130.Suppl_1.2242.2242

Published: 2017

Journal Articles

Improved Clinical Outcomes in Adults with Sickle Cell Disease and Diabetes Treated with Metformin

Sherif M. Badawy, MD, Amanda B. Payne, MPH, Sundar S. Shrestha, PhD, Scott D. Grosse, PhD

Blood (2017) 130 (Supplement 1): 3534.

https://doi.org/10.1182/blood.V130.Suppl_1.3534.3534

Published: 2017

Journal Articles

Inherited and Acquired Modifiers of Iron Status May Dramatically Affect the Phenotypic Expression of Dehydrated Hereditary Stomatocytosis

Corentin Orvain, Lydie Da Costa, MD PhD, Richard van Wijk, PhD, Serge Pissard, MD PhD, Veronique Picard, MD PhD, Lamisse Mansour-Hendili, PharmD, Muriel Giansily-Blaizot, MD PhD, Guillaume Cartron, MD PhD, Jean-Francois Schved, MD PhD, Patricia Aguilar-Martinez, MD PhD

Blood (2016) 128 (22): 1281.

https://doi.org/10.1182/blood.V128.22.1281.1281

Published: 2016

Journal Articles

A Global Delphi Consensus Initiative for Early Diagnosis of Gaucher Disease: Key Presenting Signs and Patient Co-Variables in Type 1 Disease

David J Kuter, MD DPhil, Sam Salek, PhD, Atul Mehta, MD

Blood (2016) 128 (22): 3676.

https://doi.org/10.1182/blood.V128.22.3676.3676

Published: 2016

Journal Articles

The Phenotypic Spectrum of Pyruvate Kinase Deficiency (PKD) from the PKD Natural History Study (NHS): Description of Four Severity Groups By Anemia Status

Blood (2015) 126 (23): 2136.

https://doi.org/10.1182/blood.V126.23.2136.2136

Published: 2015

Journal Articles

Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis

Thomas Pincez, Corinne Guitton, Frederic Gauthier, Guenolee Lambert, Veronique Picard, PhDMD, Madeleine feneant Thibault, Narla Mohandas, DSc, Gil Tchernia, MD, Loic Garcon

Blood (2015) 126 (23): 276.

https://doi.org/10.1182/blood.V126.23.276.276

Published: 2015

NARROW

Management of pyruvate kinase deficiency in children and adults

Relationship between Vaso-Occlusive Crises and Important Complications in Sickle Cell Disease Patients

Symptomatic Bilirubin Gallstones in Patients with PNH Treated with Eculizumab

Economic Burden of End Organ Damage Among Patients with Sickle Cell Disease in the US

Unusually High Prevalence of Silent Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease

Evaluation of Endocrine Complications in Beta-Thalassemia Intermedia Patients: A Cross Sectional Multi-Center Study

Clinical-Pathological Features of Non-Transfusion Dependent Thalassemia in Adults — a Single Center Study in Hong Kong

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

Hemolytic, Vaso-Occlusive and Renal Complications of SCD: Report from the Central Missouri Cohort

Function and dysfunction

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

An Urgent Need for Improving Thalassemia Care in Adult Patients Due to a Wide Gap on Current Real-Life Practice and Recommended Clinical Practice Guidelines

Detection of Gene Mutations in Patients with Clinically Suspected Heritary Spherocytosis By Next Generation Sequencing

Molecular Mechanism of Intrahepatic Cholestasis in Sickle Cell Disease

Effects of UGT1A1 Polymorphism, Glucose-6-Phosphate Dehydrogenase Deficiency and Deletional (-3.7кb) α-Thalassemia Among Young Nigerians with Sickle Cell Anemia

Improved Clinical Outcomes in Adults with Sickle Cell Disease and Diabetes Treated with Metformin

Inherited and Acquired Modifiers of Iron Status May Dramatically Affect the Phenotypic Expression of Dehydrated Hereditary Stomatocytosis

A Global Delphi Consensus Initiative for Early Diagnosis of Gaucher Disease: Key Presenting Signs and Patient Co-Variables in Type 1 Disease

The Phenotypic Spectrum of Pyruvate Kinase Deficiency (PKD) from the PKD Natural History Study (NHS): Description of Four Severity Groups By Anemia Status

Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis

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American Society of Hematology

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ASH Publications

American Society of Hematology

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