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Journal Articles

Splenomegaly patterns and clinical impact in African children with sickle cell anemia on hydroxyurea treatment

Leon Tshilolo, George Tomlinson, Luke Smart, Teresa Latham, Peter Olupot-Olupot, Brigida Santos, Banu Aygun, Susan Stuber, Adam Lane, Thomas Williams, Russell Ware

Blood (2025) 146 (Supplement 1): 2971.

https://doi.org/10.1182/blood-2025-2971

Published: 2025

Journal Articles

Pharmacokinetic (PK)-guided vs weight-based dosing of hydroxyurea for tanzanian children with sickle cell anemia

Luke Smart, Emmanuela Ambrose, Mwesige Charles, Kathryn McElhinney, Adam Lane, Susan Stuber, Teresa Latham, Russell Ware

Blood (2025) 146 (Supplement 1): 2959.

https://doi.org/10.1182/blood-2025-2959

Published: 2025

Journal Articles

Full assessment of clinical transfusion support (FACTS): A prospective Study to determine the burden of sickle cell anemia on pediatric blood transfusion use in a malaria-endemic region in Africa

Alexandra Power-Hays, Ruth Namazzi, Kathryn McElhinney, Abigail Kincaid, Charles Kato, Sadati Aliwuya, Robert Opoka, Andrea Conroy, Chandy John, Heather Ann Hume, Susan Stuber, Teresa Latham, Russell Ware

Blood (2025) 146 (Supplement 1): 300.

https://doi.org/10.1182/blood-2025-300

Published: 2025

Journal Articles

Biomarkers of ineffective erythropoiesis in patients with sickle cell anemia, at baseline and while treated with hydroxyurea, in comparison to patients with other iron-loading red cell disorders

Yasmin Elgammal, Lubna Hamdan, Mary Risinger, Diamantis Kostantinidis, Katie Seu, Kathryn McElhinney, Omar Niss, Elizabeta Nemeth, Charles Quinn, Russell Ware, Theodosia Kalfa

Blood (2025) 146 (Supplement 1): 4686.

https://doi.org/10.1182/blood-2025-4686

Published: 2025

Journal Articles

The ASH consa consortium on newborn screening in Africa for sickle cell disease: Interim updates of progress in screening, follow-up and supporting initiatives

Obiageli Nnodu, Bernard Awuonda, Lulu Chirande, Charles Kiyaga, Catherine Segbefia, Catherine Chunda-Liyoka, Patience Franklin, Andrew Zapfel, Marie Benoit, Alexis Thompson, Venee N. Tubman, Isaac Odame, Maureen Okam Achebe, Nancy Berliner, Theresa Coetzer, Russell Ware, Enrico Novelli, Nancy S. Green

Blood (2025) 146 (Supplement 1): 944.

https://doi.org/10.1182/blood-2025-944

Published: 2025

Journal Articles

Feasibility, reliability, and accuracy of point-of-care measurements of fetal hemoglobin

Charles Quinn, Abigail Kincaid, Kathryn McElhinney, Jennifer Korpik, Theodosia Kalfa, Russell Ware

Blood (2025) 146 (Supplement 1): 4739.

https://doi.org/10.1182/blood-2025-4739

Published: 2025

Journal Articles

Sickle cell disease is associated with early-onset clonal hematopoiesis involving DNA damage response pathway mutations

Blood (2025) 146 (Supplement 1): 8.

https://doi.org/10.1182/blood-2025-8

Published: 2025

Journal Articles

Oxidative stress and hemoglobin-c denaturation drive hemoglobin SC pathophysiology and can be ameliorated by antioxidants and hydroxyurea

Tahereh Setayesh, Anifat Tijani, Harsimran Kaur, Shristi Khanal, Zhenqi Zhu, Mengna Chi, Abigail Kincaid, Russell Ware, Punam Malik

Blood (2025) 146 (Supplement 1): 7.

https://doi.org/10.1182/blood-2025-7

Published: 2025

Journal Articles

Health status of Ugandan children born with sickle cell anemia and congenital HIV identified through newborn screening

Teresa Latham, Charles Kiyaga, Arielle Hernandez, Maria Nakafeero, Norah Kadde, Priscilla Khainza, Susan Stuber, Grace Ndeezi, Jane Aceng, Russell Ware

Blood (2025) 146 (Supplement 1): 2668.

https://doi.org/10.1182/blood-2025-2668

Published: 2025

Journal Articles

Imaging flow cytometry for detection of red blood cell inclusions: A quantitative approach to assess splenic filtration function in sickle cell disease

Cesar Rueda Rios, Miya Lu, Kristina Hanson, Ellie Savidge, Tammy Ward, Jennifer Korpik, Mary Reynaud, Russell Ware, Theodosia Kalfa, Charles Quinn

Blood (2025) 146 (Supplement 1): 1188.

https://doi.org/10.1182/blood-2025-1188

Published: 2025

Journal Articles

Measles vaccine-induced sero-protection among children with sickle cell anemia

Alexandra Power-Hays, Abigail Kincaid, Kathryn McElhinney, Teresa Latham, Charles Quinn, Robert Frenck, Russell Ware

Blood (2025) 146 (Supplement 1): 1168.

https://doi.org/10.1182/blood-2025-1168

Published: 2025

Journal Articles

Safety and efficacy of ten years of hydroxyurea treatment for young children with sickle cell anemia in Uganda

Russell Ware, Robert Opoka, Teresa Latham, Phillip Kasirye, Priscilla Kasembo, Heather Ann Hume, Isaac Birungi, Norah Kadde, Bill Wambaka, Maria Nakafeero, Adam Lane, Chandy John

Blood (2025) 146 (Supplement 1): 412.

https://doi.org/10.1182/blood-2025-412

Published: 2025

Journal Articles

Benefits of hydroxyurea in hemoglobin SC: Results of the open-label phase of the prospective identification of variables as outcomes for treatment (PIVOT) trial

Luke Smart, Yvonne Dei-Adomakoh, Adam Lane, Priscilla Ekpale, Lyudmyla Koni, Oksana Corquaye, Enoch Mensah, Susan Stuber, Teresa Latham, Catherine Segbefia, Russell Ware

Blood (2025) 146 (Supplement 1): 409.

https://doi.org/10.1182/blood-2025-409

Published: 2025

Journal Articles

Cardiac T2* Magnetic Resonance Imaging (MRI) in Iron Overload and Ventricular Diastolic Function.

Jane Hankins, MD, MS, Claudia Hillenbrand, PhD, Vijay Joshi, MD, Ralf Loeffler, PhD, Ruitian Song, PhD, Russell Ware, MD, PhD, Eileen Hansbury, PA-C, Martha Rieman, FNP, Nicole Mortier, MHS, PA-C, Matt Smeltzer, MS, Chin-Shang Li, PhD, M. Beth McCarville, MD

Blood (2007) 110 (11): 2676.

https://doi.org/10.1182/blood.V110.11.2676.2676

Published: 2007

Journal Articles

Hematopoietic Progenitor Cell Transplantation from Parental Donors for Children with Sickle Cell Anemia and Stroke.

Paul Woodard, MD, Gregory Hale, MD, Wing Leung, MD, PhD, Raymond Barfield, MD, PhD, Kimberly Kasow, DO, Renee Madden, MD, Rupert Handgretinger, MD, PhD, John Cunningham, MD, Russell Ware, MD, PhD

Blood (2007) 110 (11): 3393.

https://doi.org/10.1182/blood.V110.11.3393.3393

Published: 2007

Journal Articles

Diagnosis and management of paroxysmal nocturnal hemoglobinuria

Charles Parker, Mitsuhiro Omine, Stephen Richards, Jun-ichi Nishimura, Monica Bessler, Russell Ware, Peter Hillmen, Lucio Luzzatto, Neal Young, Taroh Kinoshita, Wendell Rosse, Gerard Socié, for the International PNH Interest Group

Blood (2005) 106 (12): 3699–3709.

https://doi.org/10.1182/blood-2005-04-1717

Published: 2005

Includes: Supplemental data

Journal Articles

Preliminary Experience with Haploidentical Stem Cell Transplantation for Children with Sickle Cell Disease and Stroke.

Joseph Woodard, MD, Winfred Wang, MD, Raymond Barfield, MD, PhD, Gregory Hale, MD, Edwin Horwitz, MD, PhD, Wing Leung, MD, PhD, Usman Yusuf, MD, Russell Ware, MD, PhD, Rupert Handgretinger, MD, John M. Cunningham, MD

Blood (2005) 106 (11): 5434.

https://doi.org/10.1182/blood.V106.11.5434.5434

Published: 2005

Journal Articles

TCD in Infants: A Report from the BABY HUG Trial.

Robert J. Adams, Julio Barredo, Duane R. Bonds, Clark Brown, James Casella, Li Daner, A.Russell Gerber, Rathi Iyer, Judy Luden, Scott Miller, Caterina Minniti, Sohail Rana, Renee Rees, Zora Rogers, Stuart Toledano, Winfred Wang, Russell Ware, Sherri Zimmerman

Blood (2005) 106 (11): 952.

https://doi.org/10.1182/blood.V106.11.952.952

Published: 2005

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Splenomegaly patterns and clinical impact in African children with sickle cell anemia on hydroxyurea treatment

Pharmacokinetic (PK)-guided vs weight-based dosing of hydroxyurea for tanzanian children with sickle cell anemia

Full assessment of clinical transfusion support (FACTS): A prospective Study to determine the burden of sickle cell anemia on pediatric blood transfusion use in a malaria-endemic region in Africa

Biomarkers of ineffective erythropoiesis in patients with sickle cell anemia, at baseline and while treated with hydroxyurea, in comparison to patients with other iron-loading red cell disorders

The ASH consa consortium on newborn screening in Africa for sickle cell disease: Interim updates of progress in screening, follow-up and supporting initiatives

Feasibility, reliability, and accuracy of point-of-care measurements of fetal hemoglobin

Sickle cell disease is associated with early-onset clonal hematopoiesis involving DNA damage response pathway mutations

Oxidative stress and hemoglobin-c denaturation drive hemoglobin SC pathophysiology and can be ameliorated by antioxidants and hydroxyurea

Health status of Ugandan children born with sickle cell anemia and congenital HIV identified through newborn screening

Imaging flow cytometry for detection of red blood cell inclusions: A quantitative approach to assess splenic filtration function in sickle cell disease

Measles vaccine-induced sero-protection among children with sickle cell anemia

Safety and efficacy of ten years of hydroxyurea treatment for young children with sickle cell anemia in Uganda

Benefits of hydroxyurea in hemoglobin SC: Results of the open-label phase of the prospective identification of variables as outcomes for treatment (PIVOT) trial

Cardiac T2* Magnetic Resonance Imaging (MRI) in Iron Overload and Ventricular Diastolic Function.

Hematopoietic Progenitor Cell Transplantation from Parental Donors for Children with Sickle Cell Anemia and Stroke.

Diagnosis and management of paroxysmal nocturnal hemoglobinuria

Preliminary Experience with Haploidentical Stem Cell Transplantation for Children with Sickle Cell Disease and Stroke.

TCD in Infants: A Report from the BABY HUG Trial.

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