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Journal Articles

Effects of Voxelotor (GBT440) Therapy on Laboratory Testing of Sickle Cell Patients

Michelle E. Savedra, MT(ASCP), Jessica L. Szuberski, MLS ASCP, Tavanna R. Porter, MS, LCGC, Molly S. Hein, Phuong L. Nguyen, MD, Min Shi, MD PhD, Aruna Rangan, MD, James D. Hoyer, MD, Jennifer L. Oliveira, MD

Blood (2019) 134 (Supplement_1): 1011.

https://doi.org/10.1182/blood-2019-131125

Published: 2019

Journal Articles

Benserazide As a Novel Fetal Hemoglobin Inducer: An Observational Study in Non-Carriers of Hemoglobin Disorders

Marina Erê A. H. P. Santos, BS, Felipe Vendrame, MSc, Alvaro Henrique Junqueira Tavares, BS, Leticia Marani, MSc, Paula C. de Azevedo, MD, Luiza G Piovesana, MD, Fernando F. Costa, MD, PhD, Kleber Yotsumoto Fertrin, MD PhD

Blood (2018) 132 (Supplement 1): 2345.

https://doi.org/10.1182/blood-2018-99-118997

Published: 2018

Journal Articles

The Optimal Cut-Off Level for Hemoglobin A2 to Differentiate between Sickle Cell Disease Genotypes

Fayiz Al Shueili, MD, Murtadha K. Al-Khabori, BSc,MD FRCPC, MSc, Salam Al-Kindi, Yasser Wali, MD, Shoaib Al-Zadjali, PhD

Blood (2018) 132 (Supplement 1): 2391.

https://doi.org/10.1182/blood-2018-99-118697

Published: 2018

Journal Articles

Spectrum of Hematological Disorders in Young Navy Recruits

Dhauna Karam, MD, Bharat L. Agrawal, MD

Blood (2017) 130 (Supplement 1): 4638.

https://doi.org/10.1182/blood.V130.Suppl_1.4638.4638

Published: 2017

Journal Articles

ASH1L: A Novel Beta-Globin Gene Regulator in Humans?

Amandine Breton, PhD, Laura Sonzogni, PhD, Andria Theodorou, PhD, Suleyman Aktuna, PhD, Stephan Menzel, PhD, Frank Grosveld, PhD, Sjaak Philipsen, PhD, Swee Lay Thein, MD DSc

Blood (2015) 126 (23): 641.

https://doi.org/10.1182/blood.V126.23.641.641

Published: 2015

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

Evaluation Of Mass Spectrometry Based Approaches For The Diagnosis Of Hemoglobinopathies

Sarah Nicolle, Nicholas Jackson, Krisztina Radi, Jane Newbold, Baharak Vafadar-Isfahani, Julia Smith, James Scrivens

Blood (2013) 122 (21): 4679.

https://doi.org/10.1182/blood.V122.21.4679.4679

Published: 2013

Journal Articles

Alfa Thalassemia Intermedia (HbH disease): How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5180.

https://doi.org/10.1182/blood.V120.21.5180.5180

Published: 2012

Journal Articles

Alfa Thalassemia Heterozygous: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5183.

https://doi.org/10.1182/blood.V120.21.5183.5183

Published: 2012

Journal Articles

Beta Thalassemia Trait: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5186.

https://doi.org/10.1182/blood.V120.21.5186.5186

Published: 2012

Journal Articles

Hereditary Spherocytosis: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Susanna Barella, MD, Ramon Simon-Lopez, MD, Nicola Di Gaetano, BS, PhD, Renzo Galanello, MD

Blood (2012) 120 (21): 5163.

https://doi.org/10.1182/blood.V120.21.5163.5163

Published: 2012

Journal Articles

Variability In Hb A2 levels among Individuals with Beta-Thalassemia Trait: Is Iron Deficiency Associated with Abnormally Low Hb A2?

Madeleine Verhovsek, MD, FRCPC, Timothy O'Shea, MD, MPH, FRCPC, Geoff Gibney, MD, Jason C.C. So, MBBS, Edmond ShiuKwan Ma, MD, FRCP, FRCPath, Li Chong Chan, MD, Martin H. Steinberg, MD, David H.K. Chui, MD

Blood (2010) 116 (21): 4281.

https://doi.org/10.1182/blood.V116.21.4281.4281

Published: 2010

Journal Articles

Newborn Haemoglobinopathy Carrier Screening: Towards Comprehensive and Improved Patient Care of Sickle Cell Disease in Oman, a Cost Effective Analysis.

Salam Alkindi, MD, Anil Pathare, MD, Ali Al Madhani, MD, Shoaib Al Zadjali, M.Sc, S. Muralitharan, Ph.D, Hamood Al Haddabi, M.Sc, Qamariya Al Abri, M.Sc, David Gravell, M.Sc, Shahina Daar, MD, J. David Dennison, MD, R. Krishnamoorthy, Ph.D

Blood (2007) 110 (11): 5155.

https://doi.org/10.1182/blood.V110.11.5155.5155

Published: 2007

Journal Articles

Four Novel Deletions in Globin Genes Revealed by Multiplex Ligation Dependent Probe Amplification Assay (MLPA) Technology.

Dvora Filon, MSc, Marion Phylipsen, BSc, Piero C. Giordano, PhD, Deborah G. Rund, MD, Cornelis L. Harteveld, PhD

Blood (2006) 108 (11): 1593.

https://doi.org/10.1182/blood.V108.11.1593.1593

Published: 2006

Journal Articles

Proteomic Detection of Beta Thalassaemia Trait Using Electrospray Mass Spectrometry-Mass Spectrometry.

Yvonne Daniel, MSc, Charles Turner, BSc, R. Neil Dalton, PhD

Blood (2005) 106 (11): 3823.

https://doi.org/10.1182/blood.V106.11.3823.3823

Published: 2005

Journal Articles

Myelofibrosis in a Patient with Sarcoidosis.

Elham Abbasi, MD, Enli Liu, MD, Martha P. Mims, MD, Phd, Mark M. Udden, MD

Blood (2005) 106 (11): 4965.

https://doi.org/10.1182/blood.V106.11.4965.4965

Published: 2005

Journal Articles

Reappraisal of Symptoms and Signs of Uncomplicated Beta Thalassemia Trait.

A. P. Premawardena, T. Malewana, M. Arambepola, N. F. Olivieri, D. J. Weatherall

Blood (2004) 104 (11): 3788.

https://doi.org/10.1182/blood.V104.11.3788.3788

Published: 2004

Journal Articles

Enhanced phagocytosis of ring-parasitized mutant erythrocytes: a common mechanism that may explain protection against falciparum malaria in sickle trait and beta-thalassemia trait

Kodjo Ayi, Franco Turrini, Antonio Piga, Paolo Arese

Blood (2004) 104 (10): 3364–3371.

https://doi.org/10.1182/blood-2003-11-3820

Published: 2004

NARROW

Effects of Voxelotor (GBT440) Therapy on Laboratory Testing of Sickle Cell Patients

Benserazide As a Novel Fetal Hemoglobin Inducer: An Observational Study in Non-Carriers of Hemoglobin Disorders

The Optimal Cut-Off Level for Hemoglobin A2 to Differentiate between Sickle Cell Disease Genotypes

Spectrum of Hematological Disorders in Young Navy Recruits

ASH1L: A Novel Beta-Globin Gene Regulator in Humans?

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

Evaluation Of Mass Spectrometry Based Approaches For The Diagnosis Of Hemoglobinopathies

Alfa Thalassemia Intermedia (HbH disease): How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Alfa Thalassemia Heterozygous: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Beta Thalassemia Trait: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Hereditary Spherocytosis: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging

Variability In Hb A2 levels among Individuals with Beta-Thalassemia Trait: Is Iron Deficiency Associated with Abnormally Low Hb A2?

Newborn Haemoglobinopathy Carrier Screening: Towards Comprehensive and Improved Patient Care of Sickle Cell Disease in Oman, a Cost Effective Analysis.

Four Novel Deletions in Globin Genes Revealed by Multiplex Ligation Dependent Probe Amplification Assay (MLPA) Technology.

Proteomic Detection of Beta Thalassaemia Trait Using Electrospray Mass Spectrometry-Mass Spectrometry.

Myelofibrosis in a Patient with Sarcoidosis.

Reappraisal of Symptoms and Signs of Uncomplicated Beta Thalassemia Trait.

Enhanced phagocytosis of ring-parasitized mutant erythrocytes: a common mechanism that may explain protection against falciparum malaria in sickle trait and beta-thalassemia trait

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American Society of Hematology

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American Society of Hematology

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