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Journal Articles

Dual Anticoagulant Facilitied Peripheral Blood Stem Cell Harvest from Childhood Donors with Low Weight and Low MCV

Li Yue, Chaoke Bu, Zhirui Ma, Chunfu Li, MD, Wenjun Wang, Jun Zhou

Blood (2019) 134 (Supplement_1): 5639.

https://doi.org/10.1182/blood-2019-129585

Published: 2019

Journal Articles

2'-O-Methoxyethyl Splice-Switching Oligos to Reverse Splicing from IVS2-745 β-Thalassemia Patient Cells: A Foundation for Potential Therapies

Blood (2019) 134 (Supplement_1): 2244.

https://doi.org/10.1182/blood-2019-127017

Published: 2019

Journal Articles

The Importance of Prenatal Diagnosis By Chorionic Villous Sampling in Detecting and Preventing Beta Haemoglobinopathies in a Resource Poor Setting: A Report from Eastern Part of India

Ankita Sen, MD, Rajib De, MD DM, Tuphan Kanti Dolai, MBBS, MD DNB, DM, Prakas Kumar Mandal, MD DM, Shyamali Dutta, MD DM, Shuvra Neel Baul, MD DM, Prantar Chakrabarti, MBBS, MDDNB, DM

Blood (2018) 132 (Supplement 1): 2348.

https://doi.org/10.1182/blood-2018-99-113120

Published: 2018

Journal Articles

Phenotypes of Hb Okayama Mutation

Rudra Ray, PhD MSc, Ankita Biswas, Msc, Sunistha Bhattacharjee, Msc, Maitreyee Bhattacharyya, DM

Blood (2018) 132 (Supplement 1): 4898.

https://doi.org/10.1182/blood-2018-99-118079

Published: 2018

Journal Articles

Mean Corpuscular Volume (MCV) and Mean Corpuscular Hemoglobin (MCH) Determinations in Newborns with Beta Thalassemia

Kaitlin Bierman, Harold M. Maurer, MD, James Harper, MD

Blood (2018) 132 (Supplement 1): 4904.

https://doi.org/10.1182/blood-2018-99-110991

Published: 2018

Journal Articles

A Retrospective Assessment of Prevention and Treatment of Iron Deficiency Amongst Patients Requiring Peripartum Transfusion

Heather Vandermeulen, MD, Yulia Lin, MD FRCPC, Anne McLeod, MD, Jon Barrett, MD, Michelle Sholzberg, MDM, MSc, FRCPC, Jeannie Callum, MD

Blood (2018) 132 (Supplement 1): 1264.

https://doi.org/10.1182/blood-2018-99-115594

Published: 2018

Journal Articles

Analysis of the Hematopoietic System in Long-Term Survivors of Allogeneic Stem Cell Transplantation and Their Respective Donors

C. Matthias Wilk, MD, Steffen Boettcher, MD, Fabian Beier, MD, Tim H. Brümmendorf, MD, Markus G Manz, MD

Blood (2017) 130 (Supplement 1): 1996.

https://doi.org/10.1182/blood.V130.Suppl_1.1996.1996

Published: 2017

Journal Articles

Traceable Red Cell Distribution Width Modifications Are Observed Prior to MDS Diagnosis and Primarily Associated with Cardiovascular Organ Dysfunction

Claudia Rodriguez, MD,, Alcedo Pedro, Sarvari Venkata Yellapragada, MD, Martha P. Mims, MD PhD, Gustavo A. Rivero, MD

Blood (2016) 128 (22): 5537.

https://doi.org/10.1182/blood.V128.22.5537.5537

Published: 2016

Journal Articles

Pathophysiology and Treatment of Beta-Thalassemia: Investigations of Heme Oxygenase 1 and Its Inhibitors

Daniel Garcia dos Santos, PhD, Zuzana Zidova, MSc, Marc Mikhael, PhD, Amel Hamdi, PhD, Monika Horvathova, PhD, Prem Ponka, MD PhD FCMA

Blood (2015) 126 (23): 3373.

https://doi.org/10.1182/blood.V126.23.3373.3373

Published: 2015

Journal Articles

Red Cell Band 3 Content Evaluation By Eosin Maleimide (EMA) Fluorescence: Beyond Diagnosis of Dominant Hereditary Spherocytosis (HS)

Ahmar Urooj Zaidi, MD, Miguel Herrera-Martinez, BS, Gerard W. Goyette, Jr., BS, Steven Buck, MS, Manisha Gadgeel, MBBS, Arathi Mohan, Bulent Ozgonenel, MD, Michael U Callaghan, MD, Robert M. Johnson, PhD, Yaddanapudi Ravindranath, MBBS

Blood (2015) 126 (23): 3343.

https://doi.org/10.1182/blood.V126.23.3343.3343

Published: 2015

Journal Articles

Predictors of Thalassaemia Carriers in Trinidad and Tobago

Sehlule Sinqobile Vuma, MD, Hasina Mayers, Bsc, George Legall, PhD

Blood (2015) 126 (23): 4569.

https://doi.org/10.1182/blood.V126.23.4569.4569

Published: 2015

Journal Articles

Impact of Immigration and Migration on Thalassemia Surveillance in California, 2004-2008

Susan Paulukonis, MA, MPH, Robert Currier, PhD, Thomas D. Coates, MD, Elliott Vichinsky, MD, Lisa Feuchtbaum, MPH, DrPH

Blood (2014) 124 (21): 4855.

https://doi.org/10.1182/blood.V124.21.4855.4855

Published: 2014

Journal Articles

DAO-2, a New Software Tool for Multiple Differential Diagnoses with Probability. Application for the Screening of Rare Anemias in Sardinia

Ramon Simon-Lopez, MD, Susanna Barella, MD

Blood (2014) 124 (21): 4905.

https://doi.org/10.1182/blood.V124.21.4905.4905

Published: 2014

Journal Articles

Uncovering the Role of Heme Oxygenase 1 in the Pathophysiology of β-Thalassemia

Daniel Garcia-Santos, PhD, Marc Mikhael, PhD, Monika Horvathova, PhD, Prem Ponka, MD PhD

Blood (2014) 124 (21): 1364.

https://doi.org/10.1182/blood.V124.21.1364.1364

Published: 2014

Journal Articles

Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β + -Thalassemia Phenotype

Ali Amid, MD, Barry Eng, BSc, Betty-Ann Hohenadel, BSc, Meredith Hanna, BSc, Lisa N. Nakamura, BSc, Lynda Walker, MLT, Melina Cheong, RN, BSc, Melanie Kirby-Allen, MBBS, John S. Waye, PhD

Blood (2014) 124 (21): 2692.

https://doi.org/10.1182/blood.V124.21.2692.2692

Published: 2014

Journal Articles

Analysis Of TMPRSS6 Polymorphisms In Patients With Iron Deficiency Anemia Partially Responsive To Oral Iron Treatment

Erika Poggiali, Fabio Andreozzi, Isabella Nava, Paola Delbini, Lorena Duca, Stella Forti, Giovanna Graziadei, Alessia Marcon, Maria Domenica Domenica Cappellini

Blood (2013) 122 (21): 3438.

https://doi.org/10.1182/blood.V122.21.3438.3438

Published: 2013

Journal Articles

Heme Oxygenase 1 Plays a Role In The Pathophysiology Of β-Thalassemia

Daniel Garcia Santos, Ph.D., Marc Mikhael, PhD, Stefano Rivella, PhD, Monika Horvathova, PhD, Prem Ponka, MD, PhD

Blood (2013) 122 (21): 3449.

https://doi.org/10.1182/blood.V122.21.3449.3449

Published: 2013

Journal Articles

Genetic Mosaicism and Hemoglobinopathies; Uniparental Isodisomy

Cornelis L Harteveld, PhD, Marion Phylipsen, PhD, Piero C Giordano, PhD

Blood (2013) 122 (21): 2258.

https://doi.org/10.1182/blood.V122.21.2258.2258

Published: 2013

Journal Articles

A Novel β Globin Gene Mutation, Reported As An α Chain Hemoglobin Variant By High Performance Liquid Chromatography (HPLC) & As Sickle Cell Trait On New Born Screening: A case Report

Kranthi Nandan Seelaboyina, MBBS, Jennifer Alison Busse, CNP, MPH, Sandeep Malik, MD, Thomas Moulton, MD

Blood (2013) 122 (21): 954.

https://doi.org/10.1182/blood.V122.21.954.954

Published: 2013

Journal Articles

Thalassemia – Increasingly Frequent Cause of Microcytic Anemias in Children in Poland

Katarzyna Albrecht, MD, PhD, Anna Adamowicz-Salach, MD, PhD, Beata Burzynska, MD, PhD, Katarzyna Pawelec, MD. PhD, Michal Matysiak, Prof.

Blood (2012) 120 (21): 5184.

https://doi.org/10.1182/blood.V120.21.5184.5184

Published: 2012

NARROW

Dual Anticoagulant Facilitied Peripheral Blood Stem Cell Harvest from Childhood Donors with Low Weight and Low MCV

2'-O-Methoxyethyl Splice-Switching Oligos to Reverse Splicing from IVS2-745 β-Thalassemia Patient Cells: A Foundation for Potential Therapies

The Importance of Prenatal Diagnosis By Chorionic Villous Sampling in Detecting and Preventing Beta Haemoglobinopathies in a Resource Poor Setting: A Report from Eastern Part of India

Phenotypes of Hb Okayama Mutation

Mean Corpuscular Volume (MCV) and Mean Corpuscular Hemoglobin (MCH) Determinations in Newborns with Beta Thalassemia

A Retrospective Assessment of Prevention and Treatment of Iron Deficiency Amongst Patients Requiring Peripartum Transfusion

Analysis of the Hematopoietic System in Long-Term Survivors of Allogeneic Stem Cell Transplantation and Their Respective Donors

Traceable Red Cell Distribution Width Modifications Are Observed Prior to MDS Diagnosis and Primarily Associated with Cardiovascular Organ Dysfunction

Pathophysiology and Treatment of Beta-Thalassemia: Investigations of Heme Oxygenase 1 and Its Inhibitors

Red Cell Band 3 Content Evaluation By Eosin Maleimide (EMA) Fluorescence: Beyond Diagnosis of Dominant Hereditary Spherocytosis (HS)

Predictors of Thalassaemia Carriers in Trinidad and Tobago

Impact of Immigration and Migration on Thalassemia Surveillance in California, 2004-2008

DAO-2, a New Software Tool for Multiple Differential Diagnoses with Probability. Application for the Screening of Rare Anemias in Sardinia

Uncovering the Role of Heme Oxygenase 1 in the Pathophysiology of β-Thalassemia

Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β + -Thalassemia Phenotype

Analysis Of TMPRSS6 Polymorphisms In Patients With Iron Deficiency Anemia Partially Responsive To Oral Iron Treatment

Heme Oxygenase 1 Plays a Role In The Pathophysiology Of β-Thalassemia

Genetic Mosaicism and Hemoglobinopathies; Uniparental Isodisomy

A Novel β Globin Gene Mutation, Reported As An α Chain Hemoglobin Variant By High Performance Liquid Chromatography (HPLC) & As Sickle Cell Trait On New Born Screening: A case Report

Thalassemia – Increasingly Frequent Cause of Microcytic Anemias in Children in Poland

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American Society of Hematology

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ASH Publications

American Society of Hematology

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