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Journal Articles

Iron Catalyzed Hydrogen Sulfide and Its Prevalence during Oxidative Events in Sickle Cell Disease

Jie Yang, PhD, Nazmin Bithi, B.Sc, Christopher Link, B.Sc, Yogenthiran Saunthararajah, MD, Christopher Hine, PhD

Blood (2019) 134 (Supplement_1): 3534.

https://doi.org/10.1182/blood-2019-122985

Published: 2019

Journal Articles

Clinical Characteristics of Brazilian Patients with Paroxysmal Nocturnal Hemoglobinuria and Changing Prognosis with Eculizumab

Patricia Eiko Yamakawa, MD, Ana Rita Da Fonseca, MD, Iara Baldim Rabelo Gomes, MD PhD, Vinicius Campos de Molla, MD, Andre Domingues Pereira, MD, Roberta Shcolnik Szor, MD, Martha Mariana Arruda, MD PhD, Maria Stella Figueiredo, MD PhD, Celso Arrais-Rodrigues, MD PhD

Blood (2019) 134 (Supplement_1): 2222.

https://doi.org/10.1182/blood-2019-132023

Published: 2019

Journal Articles

Enhanced Renal Clearance of Heme Triggers Acute Kidney Injury in Sickle Cell Disease

Samit Ghosh, PhD, Vivian Paintsil, MD, Rimi Hazra, PhD, Oluowaseun O. Orikogbo, Bethany Flage, Ezekiel Bonwin Ackah, Ellis Owusu-Dabo, PhD, Solomon Fiifi Ofori-Acquah, PhD

Blood (2017) 130 (Supplement 1): 441.

https://doi.org/10.1182/blood.V130.Suppl_1.441.441

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

Myeloid Dysfunction in Sickle Cell Disease

Alessandra Romano, MD PhD, Nunziatina Laura Parrinello, PhD, Concetta Conticello, MD, Rossellina Rosso, MD, Perrotta Caterina, Grazia Colletta, MD, Benedetta Ximenes, Piera La Cava, Carmela RITA Meli, Francesco Di Raimondo, MD

Blood (2014) 124 (21): 4908.

https://doi.org/10.1182/blood.V124.21.4908.4908

Published: 2014

Journal Articles

Value Of Magnetic Resonance Imaging In The Study and Follow-Up Of Paroxysmal Nocturnal Hemoglobinuria

Ana Villegas, Ataulfo Gonzalez, Fatima Matute, Jorge Martinez Nieto, Felix de la Fuente

Blood (2013) 122 (21): 4872.

https://doi.org/10.1182/blood.V122.21.4872.4872

Published: 2013

Journal Articles

Serum Fructosamine As an Alternative to Glycated Hemoglobin (HbA1c) for Glycemic Assessment in Diabetic Patients with Hemoglobin (Hb) Louisville

Mercedes Lorenzo-Medina, PhD, Silvia De-La-Iglesia, PhD, Lucia Quintana-Hidalgo, MD, Lidia Ruiz-Garcia, MD, Ruth Martin-Alfaro, MD, Juan Herrada, MD

Blood (2012) 120 (21): 4771.

https://doi.org/10.1182/blood.V120.21.4771.4771

Published: 2012

Journal Articles

Pro-Oxididant Induce Hemolysis in a Zebrafish Model of Glucose-6-Phosphate Dehydrogenase Deficiency.

Xiaobai Patrinostro, Ashley C Kramer, Troy Lund, MD, PhD

Blood (2012) 120 (21): 2078.

https://doi.org/10.1182/blood.V120.21.2078.2078

Published: 2012

Journal Articles

G6PD Deficient Variants Differ in Risk of Hospitalization Among Gaza Strip Palestinian Children

Noel S. Reading, PhD, Mahmoud M. Sirdah, PhD, Sherrie L. Perkins, MD, PhD, Andrew R. Wilson, MStat, Mohammad E. Shubair, PhD, Lina Aboud, MSc, Josef T. Prchal, MD

Blood (2012) 120 (21): 4268.

https://doi.org/10.1182/blood.V120.21.4268.4268

Published: 2012

Journal Articles

Long-Term Follow-up of Reduced Intensity Allogeneic Hematopoietic Stem Cell Transplantation for Severe Paroxysmal Nocturnal Hemoglobinuria

Jeremy Pantin, MD, Xin Tian, Nancy Geller, PhD, Catalina Ramos, CRN, Lisa Cook, CRN, Sophia Grasmeder, CRN, Philip Scheinberg, MD, Neal S. Young, MD, Sumithira Vasu, MD, Theresa Donohue, MHS, PA-C, Richard Childs, MD

Blood (2010) 116 (21): 3505.

https://doi.org/10.1182/blood.V116.21.3505.3505

Published: 2010

Journal Articles

Stem Cell Transplantation for Paroxysmal Nocturnal Hemoglobinuria: An on Going Joint Study of the AAWP EBMT Group and the French Society of Hematology

Régis Peffault de Latour, MD, PhD, Hubert Schrezenmeier, MD, Jean Yves Mary, PhD, Andrea Bacigalupo, MD, Carmino De Souza, MD, PhD, Roelof Willemze, MD, Andre Tichelli, MD, Jakob R. Passweg, MD, MS, Gerard Socié, MD, PhD

Blood (2008) 112 (11): 3442.

https://doi.org/10.1182/blood.V112.11.3442.3442

Published: 2008

Journal Articles

Clinical Features for Heterozygosity of the Common β Globin Gene Frameshift 41/42 Mutation: Identification and Properties of Hb Salouël (β[Phe41Leu;Val59X])

Jacques Rochette, Estelle Cadet, Francis Boitte, Najeh El Esper, Claire Presne, Patricia Bignet, Christine Cézard

Blood (2008) 112 (11): 4794.

https://doi.org/10.1182/blood.V112.11.4794.4794

Published: 2008

Journal Articles

Development and Validation of a Pediatric Severity Index for Sickle Cell Patients.

Xandra W. van den Tweel, MD, Johanna H. van der Lee, MD, Harriët Heijboer, MD PhD, Marjolein Peters, MD PhD, Karin Fijnvandraat, MD PhD

Blood (2007) 110 (11): 3391.

https://doi.org/10.1182/blood.V110.11.3391.3391

Published: 2007

Journal Articles

Impaired CD163 Mediated Hemoglobin-Scavenging and Hemolytic Crisis in Patients Treated with CD33 Targeted Chemotherapy (Gemtuzumab Ozogamicin, Mylotarg™).

Maciej B. Maniecki, MHSc, Henrik Hasle, MD, PHD, Lennart Friis-Hansen, MD, PHD, Birgitte Lausen, MD, PHD, Ove J. Nielsen, MD, PHD, Knud Bendix, MD, PHD, Soren K. Moestrup, MD, PHD, Holger J. Moller, MD, PHD

Blood (2007) 110 (11): 3684.

https://doi.org/10.1182/blood.V110.11.3684.3684

Published: 2007

Journal Articles

Microalbuminuria among Egyptian Children and Adult with Sickle Cell Hemoglobinopathy, Single Institution Study.

Wafaa E. Ibrahim, MD, Ashraf M. Abdelmonem, MD, Nermin H. Mahmoud, MD, Waleed Mostafa, MD

Blood (2006) 108 (11): 3361.

https://doi.org/10.1182/blood.V108.11.3361.3361

Published: 2006

Journal Articles

Management of Hereditary Spherocytosis in a Public Health Care Provider in a Developing Country.

Leonardo Feldman, MD, Guillermo Drelichman, MD, Nora Basack, MD, Ernesto Rodriguez, MD, Daniel Freigeiro, MD, Luis Aversa, MD

Blood (2005) 106 (11): 3752.

https://doi.org/10.1182/blood.V106.11.3752.3752

Published: 2005

Journal Articles

The Graft-vs-Host Hematopoietic Effect Generated after Nonmyeloablative Allogeneic Stem Cell Transplantation (NST) Cures Patients with Severe PNH.

Yoshiyuki Takahashi, MD, PhD, S. Chakrabarti, MD, R. Srinivasan, MD, PhD, T. Igarashi, MD, PhD, A. Lundqvist, PhD, I. Espinoza, MD, D. Suffredini, J.P. McCoy, Jr., PhD, A.J. Barrett, MD, N.S. Young, MD, Richard Childs, MD

Blood (2004) 104 (11): 811.

https://doi.org/10.1182/blood.V104.11.811.811

Published: 2004

Journal Articles

Potential Value of N-Desulfated Heparin without Anticoagulant Activity in Treatment of Complement-Mediated Lysis of Paroxysmal Nocturnal Hemoglobinuria Erythrocytes.

Haruhiko Ninomiya, MD, Toshiro Nagasawa, MD

Blood (2004) 104 (11): 2826.

https://doi.org/10.1182/blood.V104.11.2826.2826

Published: 2004

Journal Articles

Diagnosis of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in the Negro Male Despite Hemolytic Crisis

FRITZ HERZ, PH.D., EUGENE KAPLAN, M.D., ELSIE S. SCHEYE, MT (ASCP)

Blood (1970) 35 (1): 90–93.

https://doi.org/10.1182/blood.V35.1.90.90

Published: 1970

NARROW

Iron Catalyzed Hydrogen Sulfide and Its Prevalence during Oxidative Events in Sickle Cell Disease

Clinical Characteristics of Brazilian Patients with Paroxysmal Nocturnal Hemoglobinuria and Changing Prognosis with Eculizumab

Enhanced Renal Clearance of Heme Triggers Acute Kidney Injury in Sickle Cell Disease

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

Myeloid Dysfunction in Sickle Cell Disease

Value Of Magnetic Resonance Imaging In The Study and Follow-Up Of Paroxysmal Nocturnal Hemoglobinuria

Serum Fructosamine As an Alternative to Glycated Hemoglobin (HbA1c) for Glycemic Assessment in Diabetic Patients with Hemoglobin (Hb) Louisville

Pro-Oxididant Induce Hemolysis in a Zebrafish Model of Glucose-6-Phosphate Dehydrogenase Deficiency.

G6PD Deficient Variants Differ in Risk of Hospitalization Among Gaza Strip Palestinian Children

Long-Term Follow-up of Reduced Intensity Allogeneic Hematopoietic Stem Cell Transplantation for Severe Paroxysmal Nocturnal Hemoglobinuria

Stem Cell Transplantation for Paroxysmal Nocturnal Hemoglobinuria: An on Going Joint Study of the AAWP EBMT Group and the French Society of Hematology

Clinical Features for Heterozygosity of the Common β Globin Gene Frameshift 41/42 Mutation: Identification and Properties of Hb Salouël (β[Phe41Leu;Val59X])

Development and Validation of a Pediatric Severity Index for Sickle Cell Patients.

Impaired CD163 Mediated Hemoglobin-Scavenging and Hemolytic Crisis in Patients Treated with CD33 Targeted Chemotherapy (Gemtuzumab Ozogamicin, Mylotarg™).

Microalbuminuria among Egyptian Children and Adult with Sickle Cell Hemoglobinopathy, Single Institution Study.

Management of Hereditary Spherocytosis in a Public Health Care Provider in a Developing Country.

The Graft-vs-Host Hematopoietic Effect Generated after Nonmyeloablative Allogeneic Stem Cell Transplantation (NST) Cures Patients with Severe PNH.

Potential Value of N-Desulfated Heparin without Anticoagulant Activity in Treatment of Complement-Mediated Lysis of Paroxysmal Nocturnal Hemoglobinuria Erythrocytes.

Diagnosis of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in the Negro Male Despite Hemolytic Crisis

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American Society of Hematology

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ASH Publications

American Society of Hematology

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