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Journal Articles

High Hemoglobin F in Sickle Cell Disease: Waning Protection with Age

Seda S. Tolu, MD, Morayma Reyes Gil, MD PhD, Ugochi Olivia Ogu, MD, Jui Choudhuri, MD, Roger Fecher, MD, Gracy Sebastian, NP, Caterina P. Minniti, MD

Blood (2019) 134 (Supplement_1): 3576.

https://doi.org/10.1182/blood-2019-122387

Published: 2019

Journal Articles

Genetic Analysis in the Tanzania Sickle Surveillance Study (TS3): Modifiers of Sickle Cell Disease and Identification of Hemoglobin Variants

Luke R. Smart, MD, Emmanuela E. Ambrose, MD, Mwesige Charles, BScHLS, Arielle G. Hernandez, MPH, Teresa S. Latham, MA, Adolfine Hokororo, MD MMed, MSc, Medard Beyanga, BLS, MSc, Erasmus Kamugisha, MD MSc, PhD, Erius Tebuka, MD MMed, Thad A. Howard, MS, Russell E. Ware, MD PhD

Blood (2019) 134 (Supplement_1): 988.

https://doi.org/10.1182/blood-2019-128554

Published: 2019

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

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

The Use of Marijuana and Hydroxyurea Among Sickle Cell Patients

Nene Kalu, LGSW, Patricia A. O'Neal, MD, Catherine Nwokolo, RN, Sharmin Diaz, FNP, Oluwakemi Owoyemi, MD MPH

Blood (2016) 128 (22): 5913.

https://doi.org/10.1182/blood.V128.22.5913.5913

Published: 2016

Journal Articles

Genetic Analyses in the Uganda Sickle Surveillance Study: Modifiers of Sickle Cell Anemia and Identification of Hemoglobin Variants

Beverly A Schaefer, MD, Charles Kiyaga, MS MPhil, Thad A. Howard, MS, Grace Ndeezi, MBChB PhD, Arielle G Hernandez, MPH, Isaac Ssewanyana, MS, Mary C. Paniagua, MA, Christopher Ndugwa, MBChB, Jane Aceng, MBChB MPH, Russell E. Ware, MD PhD

Blood (2016) 128 (22): 2479.

https://doi.org/10.1182/blood.V128.22.2479.2479

Published: 2016

Journal Articles

The Prevalence of Hereditary Hemoglobin Disorders and Its Implications for Newborn Screening in Germany

Regine Grosse, MD, Reinhard Schneppenheim, MD PhD, Zoltan Lukacs, PhD, Florian Oyen, Birgit Muntau, Paulina Lukacs, PhD, Bernd Noack, MD

Blood (2014) 124 (21): 4071.

https://doi.org/10.1182/blood.V124.21.4071.4071

Published: 2014

Journal Articles

Iron Deficiency Anemia in Infants and Toddlers – Role of Milk and Constipation

Madhavi Lakkaraja, MD, Lesley Small, MD, Maura Frank, MD, Aliza Solomon, DO, Nicole Kucine, MD, James B Bussel, MD

Blood (2012) 120 (21): 5171.

https://doi.org/10.1182/blood.V120.21.5171.5171

Published: 2012

Journal Articles

Nine Novel Mutations in the Erythroid Transcription Factor KLF1 Gene Associated with Increased Fetal Hemoglobin Levels in Adults,

Alice Gallienne, MSc, Helene Dreau, MSc, Anna Schuh, PhD, Chris S.R Hatton, MD, John Old, PhD, Shirley Henderson, PhD

Blood (2011) 118 (21): 3191.

https://doi.org/10.1182/blood.V118.21.3191.3191

Published: 2011

Journal Articles

Evaluation of Low Mean Corpuscular Volume in an Apheresis Donor Population.

Barbara J. Bryant, MD, Julie A. Hopkins, RN, Susan F. Leitman, MD

Blood (2006) 108 (11): 4136.

https://doi.org/10.1182/blood.V108.11.4136.4136

Published: 2006

Journal Articles

Presence of Alpha Thalassemia Trait Complicating the Diagnosis of Polycythemia Vera in a Pediatric Patient.

Shannon L. Carpenter, MD, Howard A. Britton, MD, Josef T. Prchal, MD, Martha P. Mims, MD, PhD

Blood (2005) 106 (11): 3847.

https://doi.org/10.1182/blood.V106.11.3847.3847

Published: 2005

NARROW

High Hemoglobin F in Sickle Cell Disease: Waning Protection with Age

Genetic Analysis in the Tanzania Sickle Surveillance Study (TS3): Modifiers of Sickle Cell Disease and Identification of Hemoglobin Variants

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

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

The Use of Marijuana and Hydroxyurea Among Sickle Cell Patients

Genetic Analyses in the Uganda Sickle Surveillance Study: Modifiers of Sickle Cell Anemia and Identification of Hemoglobin Variants

The Prevalence of Hereditary Hemoglobin Disorders and Its Implications for Newborn Screening in Germany

Iron Deficiency Anemia in Infants and Toddlers – Role of Milk and Constipation

Nine Novel Mutations in the Erythroid Transcription Factor KLF1 Gene Associated with Increased Fetal Hemoglobin Levels in Adults,

Evaluation of Low Mean Corpuscular Volume in an Apheresis Donor Population.

Presence of Alpha Thalassemia Trait Complicating the Diagnosis of Polycythemia Vera in a Pediatric Patient.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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