Results 211 to 220 of about 94,881 (302)

Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments

, 2019
Luis E.F. Almeida, Sayuri Kamimura, Celia M. de Souza Batista, Nicholas Spornick, Margaret Nettleton, Elizabeth Walek, Meghann L. Smith, Julia C. Finkel, Deepika S. Darbari, Paul Wakim, Zenaide Quezado   +10 more
openalex   +2 more sources

Hypomorphic ATP11c is a novel regulator of decreased efficacy of transfused red blood cells in humans and mice

HemaSphere, Volume 10, Issue 1, January 2026.
Abstract Chronic red blood cell (RBC) transfusion sustains patients with diverse hematologic disorders, but repeated transfusion leads to iron overload and alloimmunization. Reducing transfusion burden requires identifying donor units that circulate more effectively after storage, yet determinants of this variability remain incompletely defined.
James C. Zimring, Ariel M. Hay, Monika Dzieciatkowska, Daniel Stephenson, Zachary B. Haiman, Steven Kleinman, Philip J. Norris, Michael P. Busch, Nareg Roubinian, Elisa Fermo, Paola Bianchi, Gregory R. Keele, Grier P. Page, Angelo D'Alessandro   +13 more
wiley   +1 more source

The ASH Research Collaborative Sickle Cell Disease Research Network: past, present, and future. [PDF]

Blood Adv
El Rassi F, Andemariam B, Kutlar A, Pace BS, Fink A, Torres K, Dowd C, Abrams CS.   +7 more
europepmc   +1 more source

Erythropoiesis in health and disease: Distinguishing defective and ineffective erythropoiesis

HemaSphere, Volume 10, Issue 1, January 2026.
Abstract Erythropoiesis is a finely regulated process ensuring continuous red blood cell production to maintain oxygen delivery. Disruptions in this process give rise to defective erythropoiesis, characterized by impaired lineage commitment and progenitor development, and ineffective erythropoiesis (IE), marked by expansion of erythroid progenitors ...
Sara El Hoss, Maria A. Lizarralde‐Iragorri, Thiago Trovati Maciel, Olivier Hermine   +3 more
wiley   +1 more source

Unravelling the Immunological Enigma of Sickle Cell Disease: Current Understanding and Future Directions. [PDF]

Immunology
Jamwal S, Calhoun C, Mohanty S, Montgomery RR, Krishnamurti L, Shaw AC, Yildirim I.   +6 more
europepmc   +1 more source

Red blood cell storage duration is not associated with clinical outcomes for acute chest syndrome in children with sickle cell disease

, 2015
Melanie E. Fields, Monica L. Hulbert, Ling Chen, Ari N. Berlin, Ron Jackups, Philip C. Spinella   +5 more
openalex   +2 more sources

Knowledge, Attitudes, Practices, and Misconceptions Regarding Vitamins in Blood Metabolism and Anemia Among University Students: A One Center Cross‐Sectional Study in Ghana

Health Science Reports, Volume 9, Issue 1, January 2026.
ABSTRACT Background In Sub‐Saharan Africa, anemia is a significant public health issue, affecting individuals of all ages. While prevention efforts focus on infants, children, and pregnant women, adolescents are overlooked often, leading to ongoing challenges.
David Mawutor Donkor, Gideon Owusu, Victoria Essuon‐Sepah, Obed Asamoah, Isabella Anokye, Alfred Kwadwo Sah, Safianu Apalebilah, Patrick Adu, Joseph Boachie   +8 more
wiley   +1 more source

Functional capacity in sickle cell disease: A pilot study with 1-minute sit-to-stand test. [PDF]

Hematol Transfus Cell Ther
Thomaz MB, Suassuna LF, Fabri JC, Araújo IO, Almeida JC, Rodrigues DOW.   +5 more
europepmc   +1 more source

Assessment of Safety and Efficacy of PBSC Mobilization with G-CSF and CD34+ Enrichment and Pbmnc (CD3+) Addback in Familial Haploidentical (FHI) Adult Donors with Sickle Cell Disease Trait (SCDT) Prior to Allogeneic HSCT of High-Risk SCD Patients

, 2019
Bronwyn Long, Allyson Flower, Sandra Fabricatore, Erin Morris, Harshini Mahanti, Qiuhu Shi, Carolyn A. Keever-Taylor, Rona Singer Weinberg, Brenda J. Grossman, Julie‐An Talano, Shalini Shenoy, Theodore B. Moore, Janet Ayello, Mildred Semidei‐Pomales, Carmella van de Ven, Mitchell S. Cairo   +15 more
openalex   +1 more source

Frequency and Associated Factors of Clotted and Hemolyzed Samples in South Gonder Hospitals, Ethiopia: A Multicenter Cross‐Sectional Study, 2023

Journal of Clinical Laboratory Analysis, Volume 40, Issue 2, January 2026.
This study, conducted in South Gonder hospitals in Ethiopia, investigated the prevalence and causes of clotted and hemolyzed blood samples submitted for hematological testing. The findings revealed a high rate of sample quality issues, with significant associations identified between pre‐analytical factors like collection technique and sample integrity.
Birhanemaskal Malkamu, Getaneh Atikilt Yemata, Andargachew Almaw, Ayenew Assefa, Birhanu Getie, Teklehaimanot Kiros, Mulat Erkihun, Shewaneh Damtie, Tegenaw Tiruneh, Berhanu Abebaw Mekonnen, Meron Asmamaw Alemayehu, Abraham Teym, Abathun Temesgen, Gashaw Melkie Bayeh, Almaw Genet Yeshiwas, Rahel Mulatie Anteneh, Melkamu Aderajew Zemene, Tesfaneh Shimels, Chalachew Yenew, Wolde Melese Ayele, Ahmed Fentaw Ahmed, Assefa Andargie Kassa, Tilahun Degu Tsega, Chalachew Abiyu Ayalew, Sintayehu Simie Tsega, Zeamanuel Anteneh Yigzaw, Amare Genetu Ejigu, Wondimnew Desalegn Addis, Getasew Yirdaw, Kalaab Esubalew Sharew, Daniel Adane, Samuel Berihun Dagnew, Gebyaw Arega, Habitamu Mekonen   +33 more
wiley   +1 more source