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Journal Articles

Coinheritance of Alpha -3.7 Deletion and Hb Questembert [ 131 alpha-2 Tct > CCT](Ser131>Pro)] in an African American Patient Results in an Alpha Thalassemia Phenotype

Asiya Shakir, MD, Betty Pace, MD, Niren Patel, MBBS, Ferdane Kutlar, MD, Abdullah Kutlar, MD, Afshin Ameri, MD

Blood (2015) 126 (23): 4597.

https://doi.org/10.1182/blood.V126.23.4597.4597

Published: 2015

Journal Articles

Hemoglobinopathies Of Difficult Diagnosis. Case Reports From a Main Referral Pediatric Hospital In Venezuela

Adriana C. Bello, MD

Blood (2013) 122 (21): 4698.

https://doi.org/10.1182/blood.V122.21.4698.4698

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

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

Hemoglobin Agenogi in Argentina: Case Report

Ana Paula Martin, Sr., Patricia Martha Gargallo, Irma Margarita Bragos, Bioquimica, Alejandro Abbate, Mara Jorgelina Ojeda, Verónica Susana Montero

Blood (2012) 120 (21): 4776.

https://doi.org/10.1182/blood.V120.21.4776.4776

Published: 2012

Journal Articles

Phenotypic Evaluation of a Family Cohort with Hemolytic Anemia

Brett L. Houston, BSc, Donald S. Houston, MD, Ph.D, Sara J. Israels, MD, Gail Coghlan, Bernie N. Chodirker, MD, Teresa Zelinski, Ph.D, Ryan Zarychanski, MD, MSc

Blood (2010) 116 (21): 3214.

https://doi.org/10.1182/blood.V116.21.3214.3214

Published: 2010

Journal Articles

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

Kavita Natarajan, Niren Patel, MBBS, Lina Zhuang, MD, Harris Carmichael, Elizabeth Manaloor, MD, Abdullah Kutlar, MD, Ferdane Kutlar, MD

Blood (2010) 116 (21): 4814.

https://doi.org/10.1182/blood.V116.21.4814.4814

Published: 2010

Journal Articles

Plasma Protein Oxidation and Triglyceride Levels in Sickle Cell Anemia.

Yesim Oztas, MD, Selma Unal, MD, Nuriman Ozgunes, PhD

Blood (2009) 114 (22): 2578.

https://doi.org/10.1182/blood.V114.22.2578.2578

Published: 2009

Journal Articles

Endothelial Activation by Sickle Mouse Red Cells and Their Endothelial Adhesion In Vivo is Abolished by Catalase Treatment of Sickle Cells, but Not Quiescent Endothelium, Implying a Role of Heme-Mediated Peroxide Generation in Sickle Cell Adhesion.

Dhananjay K. Kaul, PhD, Sandra M. Suzuka, MS, Mary Fabry, PhD

Blood (2009) 114 (22): 902.

https://doi.org/10.1182/blood.V114.22.902.902

Published: 2009

Journal Articles

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Anna P. Marcello, PhD, Cristina Vercellati, PhD, Elisa Fermo, PhD, Paola Bianchi, PhD, Wilma Barcellini, MD, Alberto Zanella, MD

Blood (2007) 110 (11): 1738.

https://doi.org/10.1182/blood.V110.11.1738.1738

Published: 2007

Journal Articles

Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy.

Aurora Feliu-Torres, MD, S. Eandi-Eberle, Biochemistry, K. Calvo, Biochemistry, I. Bragós, Biochemistry, M. Ojeda, Biochemistry, M. Voss, Biochemistry, A. Pratti, Biochemistry, A. Milani, Biochemistry, H. Targovnik, MD, G. Sciuccati, MD, M. Bonduel, MD, L. Diaz, MD, R. Staciuk, MD, N. Noguera, Biochemistry

Blood (2007) 110 (11): 3806.

https://doi.org/10.1182/blood.V110.11.3806.3806

Published: 2007

Journal Articles

Antioxidant Status of Red Blood Cells Is a Modifying Factor of Clinical Manifestation of Unstable Hemoglobin Variant Hana [α2β2 63 (E7) His-Asn)].

Renata Solna, PhD, Petr Dolezel, PhD, Petr Mlejnek, PhD, Vladimir Divoky, PhD

Blood (2006) 108 (11): 3789.

https://doi.org/10.1182/blood.V108.11.3789.3789

Published: 2006

Journal Articles

Application of the Luminex Platform for Multiplexed Genotyping of Non-Deletional Alpha Thalassemia Mutations.

Sharon Aslanian, MS, Azimi Mahin, CLS, Carolyn Hoppe, MD

Blood (2005) 106 (11): 3841.

https://doi.org/10.1182/blood.V106.11.3841.3841

Published: 2005

Journal Articles

Ten Year-Old Male with Hemoglobin Lufkin/Beta-Zero Thalassemia Compound Heterozygote Who Exhibited Beta-Thalassemia Major Characteristics.

Ahna M. Blutreich, MD, Peihong Shu, MD, Jeremy S. Bragdon, MD, Paul J. Kurtin, MD, James D. Hoyer, MD, Gungor Karayalcin, MD

Blood (2005) 106 (11): 3815.

https://doi.org/10.1182/blood.V106.11.3815.3815

Published: 2005

Journal Articles

Hemoglobin Ville-Marie: A New β-Globin Variant (del480C) Causing Oxydative Hemolysis.

Celine Devaux, MD, Pierre Chagnon, PhD, Claude Belisle, M.Sc., Denis Soulieres, MD, M.Sc., Lambert Busque, MD

Blood (2005) 106 (11): 3783.

https://doi.org/10.1182/blood.V106.11.3783.3783

Published: 2005

Journal Articles

DNA Sequence of Hemoglobin Chico.

Aaron M. Fond, Stephen Neville, MD, John Gotchall, MD, Enli Liu, MD, Ching-Nan Ou, PhD, Cheryl L. Rognerud, Martha P. Mims, MD, PhD

Blood (2005) 106 (11): 3784.

https://doi.org/10.1182/blood.V106.11.3784.3784

Published: 2005

Journal Articles

Alpha Hemoglobin Stabilizing Protein (AHSP) Is a Susceptibility Gene to Drug /Infection-Induced Hemolytic Anemia.

Hitoshi Kanno, MD, PhD, Naoyuki Kamatani, MD, PhD, Takako Hamada, Kaori Furihata, PhD, Yukio Hattori, MD, PhD, Shiro Miwa, MD, PhD, Hisaichi Fujii, MD, PhD

Blood (2005) 106 (11): 1678.

https://doi.org/10.1182/blood.V106.11.1678.1678

Published: 2005

Journal Articles

HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia.

Maria F. Sonati, PhD, Beatriz I. Weinstein, PhD, Beatriz Erramouspe, Dulcineia M. Albuquerque, MSc, Elza M. Kimura, MSc, Denise M. Oliveira, Fernando F. Costa

Blood (2004) 104 (11): 3776.

https://doi.org/10.1182/blood.V104.11.3776.3776

Published: 2004

NARROW

Coinheritance of Alpha -3.7 Deletion and Hb Questembert [ 131 alpha-2 Tct > CCT](Ser131>Pro)] in an African American Patient Results in an Alpha Thalassemia Phenotype

Hemoglobinopathies Of Difficult Diagnosis. Case Reports From a Main Referral Pediatric Hospital In Venezuela

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

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

Hemoglobin Agenogi in Argentina: Case Report

Phenotypic Evaluation of a Family Cohort with Hemolytic Anemia

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

Plasma Protein Oxidation and Triglyceride Levels in Sickle Cell Anemia.

Endothelial Activation by Sickle Mouse Red Cells and Their Endothelial Adhesion In Vivo is Abolished by Catalase Treatment of Sickle Cells, but Not Quiescent Endothelium, Implying a Role of Heme-Mediated Peroxide Generation in Sickle Cell Adhesion.

Coexistence of Congenital Red Cell Pyruvate Kinase Deficiency and Hereditary Stomatocytosis.

Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy.

Antioxidant Status of Red Blood Cells Is a Modifying Factor of Clinical Manifestation of Unstable Hemoglobin Variant Hana [α2β2 63 (E7) His-Asn)].

Application of the Luminex Platform for Multiplexed Genotyping of Non-Deletional Alpha Thalassemia Mutations.

Ten Year-Old Male with Hemoglobin Lufkin/Beta-Zero Thalassemia Compound Heterozygote Who Exhibited Beta-Thalassemia Major Characteristics.

Hemoglobin Ville-Marie: A New β-Globin Variant (del480C) Causing Oxydative Hemolysis.

DNA Sequence of Hemoglobin Chico.

Alpha Hemoglobin Stabilizing Protein (AHSP) Is a Susceptibility Gene to Drug /Infection-Induced Hemolytic Anemia.

HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia.

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American Society of Hematology

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American Society of Hematology

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