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1-20 of 39
Keywords: Sickle cell anemia
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Journal Articles
Pharmacokinetic-Guided Hydroxyurea to Reduce Transfusions in Ugandan Children with Sickle Cell Anemia: Study Design of the Alternative Dosing And Prevention of Transfusions Trial
Available to PurchaseAlexandra Power-Hays, Ruth Namazzi, Charles Kato, Kathryn E. McElhinney, Andrea L. Conroy, Heather Hume, Chandy John, Sara M. O'Hara, Susan E. Stuber, Adam Lane, Teresa S. Latham, Robert O. Opoka, Russell E. Ware
Journal:
Acta Haematologica
Acta Haematol (2025) 148 (2): 208–219.
Published Online: 05 June 2024
...Alexandra Power-Hays; Ruth Namazzi; Charles Kato; Kathryn E. McElhinney; Andrea L. Conroy; Heather Hume; Chandy John; Sara M. O'Hara; Susan E. Stuber; Adam Lane; Teresa S. Latham; Robert O. Opoka; Russell E. Ware Introduction: People with sickle cell anemia (SCA) may require frequent blood...
Journal Articles
Stroke Prevention with Hydroxyurea Enabled through Research and Education: A Phase 2 Primary Stroke Prevention Trial in Sub-Saharan Africa
Available to PurchaseLuke R. Smart, Emmanuela E. Ambrose, Georgina Balyorugulu, Primrose Songoro, Idd Shabani, Protas Komba, Mwesige Charles, Thad A. Howard, Kathryn E. McElhinney, Sara M. O’Hara, Jodie Odame, Maria Nakafeero, Janet Adams, Susan E. Stuber, Adam Lane, Teresa S. Latham, Abel N. Makubi, Russell E. Ware
Journal:
Acta Haematologica
Acta Haematol (2023) 146 (2): 95–105.
Published Online: 20 April 2023
... Introduction: Stroke is a severe complication of sickle cell anemia (SCA), with devastating sequelae. Transcranial Doppler (TCD) ultrasonography predicts stroke risk, but implementing TCD screening with suitable treatment for primary stroke prevention in low-resource environments remains challenging. SPHERE...
Journal Articles
Pediatric to Adult Transition in Sickle Cell Disease: Survey Results from Young Adult Patients
Available to PurchaseKate Travis, Anthony Wood, Peter Yeh, Sachin Allahabadi, Ling-Chen Chien, Sara Curtis, Allexa Hammond, Jaden Kohn, Christine Ogugbuaja, Matthew Rees, John Shumway, Vivien Sheehan
Journal:
Acta Haematologica
Acta Haematol (2020) 143 (2): 163–175.
Published Online: 15 July 2019
... ]. Sickle cell anemia Sickle cell disease Quality of life Transition Outcomes Pediatrics Adult Survey © 2019 S. Karger AG, Basel 2019 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced...
Journal Articles
ANTXR1 Intronic Variants Are Associated with Fetal Hemoglobin in the Arab-Indian Haplotype of Sickle Cell Disease
Available to PurchaseZhara A. Al-Ali, Rana K. Fallatah, Esra A. Aljaffer, Eman R. Albukhari, Neriman Sadek Al-Ali, Ziyad T. Al-Ghannam, Reem Sayeb Al-Atrash, Ahmed Alsuliman, Chittibabu Vatte
Journal:
Acta Haematologica
Acta Haematol (2018) 140 (1): 55–59.
Published Online: 16 August 2018
...Zhara A. Al-Ali; Rana K. Fallatah; Esra A. Aljaffer; Eman R. Albukhari; Neriman Sadek Al-Ali; Ziyad T. Al-Ghannam; Reem Sayeb Al-Atrash; Ahmed Alsuliman; Chittibabu Vatte Disease severity of sickle cell anemia is highly variable, and it is commonly accepted that fetal hemoglobin (HbF) levels play...
Journal Articles
Hydroxyurea Increases Plasma Concentrations of Microparticles and Reduces Coagulation Activation and Fibrinolysis in Patients with Sickle Cell Anemia
Available to PurchaseDenise Menezes Brunetta, Gil Cunha De Santis, Ana Cristina Silva-Pinto, Luciana Correa Oliveira de Oliveira, Dimas Tadeu Covas
Journal:
Acta Haematologica
Acta Haematol (2015) 133 (3): 287–294.
Published Online: 02 December 2014
...]. There was no difference (p = 0.1003) in the concentration of MPs derived from platelets between these two groups. Hemostasis Hydroxyurea Microparticles Sickle cell anemia Sickle cell anemia (SCA) is associated with abnormal activation of the coagulation cascade, which is clearly evidenced by the increased...
Journal Articles
Thalassemia Major and Sickle Cell Disease in Adolescents and Young Adults
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (2014) 132 (3-4): 340–347.
Published Online: 10 September 2014
... with dedicated support staff [ 81 ]. Adolescence Care transition Sickle cell anemia Thalassemia major Young adults Adolescents and young adults (AYAs) with thalassemia major (TM) and sickle cell disease (SCD) pose unique challenges in their medical treatment. Improved availability of medical...
Journal Articles
Structural Modification of Plasma Albumin in Sickle Cell Anemia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (2014) 133 (1): 67–69.
Published Online: 15 August 2014
... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Protein chemistry Sickle cell anemia Sickle cell anemia (SCA...
Journal Articles
Two-Year Analysis of Efficacy and Safety of Deferasirox Treatment for Transfusional Iron Overload in Sickle Cell Anemia Patients
Available to PurchaseRodolfo Cancado, Maria Cristina A. Olivato, Paula Bruniera, Gilberto Szarf, Roberto de Moraes Bastos, Murilo Rezende Melo, Carlos Chiattone
Journal:
Acta Haematologica
Acta Haematol (2012) 128 (2): 113–118.
Published Online: 30 June 2012
...Rodolfo Cancado; Maria Cristina A. Olivato; Paula Bruniera; Gilberto Szarf; Roberto de Moraes Bastos; Murilo Rezende Melo; Carlos Chiattone The efficacy and safety of a 2-year treatment with deferasirox was evaluated in 31 patients with sickle cell anemia and transfusional iron overload. At 24...
Journal Articles
Practical Diagnosis of Red Cell Disorders in Southern Spain
Available to PurchaseM.A. Molina-Arrebola, C. Avivar-Oyonarte, J. Salas-Coronas, R. Pérez-Moyano, M.J. Giménez-López, J.A. García-Bautista, A.M. Jiménez-Gila, C. Porrino-Herrera
Journal:
Acta Haematologica
Acta Haematol (2011) 127 (1): 50–55.
Published Online: 25 October 2011
... to be devised. 21 02 2011 3 08 2011 25 10 2011 Fourteen patients with homozygous Hb SS were diagnosed, all because of symptoms related to sickle cell anemia, such as hemolytic crisis, acute chest syndrome, dactylitis, aseptic bone necrosis, and pain crisis. Five patients presented...
Journal Articles
β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ⁰-Thalassemia and Their Association with Clinical and Hematological Features
Available to PurchaseAndré Rolim Belisário, Marina Lobato Martins, Ana Mercy Siebra Brito, Cibele Velloso Rodrigues, Célia Maria Silva, Marcos Borato Viana
Journal:
Acta Haematologica
Acta Haematol (2010) 124 (3): 162–170.
Published Online: 12 October 2010
.... Furthermore, β S -haplotypes CAR and Ben were not associated with any analyzed feature of children with sickle cell anemia. 10 05 2010 16 08 2010 12 10 2010 © 2010 S. Karger AG, Basel 2010 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part...
Journal Articles
Metabolic Activity of Polymorphonuclear Leukocytes in Sickle Cell Anemia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1972) 47 (5): 283–291.
Published Online: 05 March 2009
...N.V. Dimitrov; F.R. Douwes; Barbara Bartolotta; S. Nochumson; Mary Ann Toth Polymorphonuclear (PMN) leukocytes from patients with sickle cell anemia and a history of repeated infection failed to show a stimulation of respiratory CO 2 , O 2 consumption, oxidation of formate and reduction...
Journal Articles
Hemoglobin S-Gα Georgia Disease: A Case Report
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1974) 51 (5): 315–320.
Published Online: 04 March 2009
... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hb Gα Georgia Hb S-Gα Georgia Hemoglobin interactions Hemoglobinopathies Sickle cell anemia Acta Haemat. 51: 315...
Journal Articles
Splenic Function and Infection in Sickle Cell Anemia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1973) 50 (3): 154–161.
Published Online: 04 March 2009
...Maria L. Falter; Margaret G. Robinson; O. Ok Soon Kim; S. Suat Cheng Go; S.P. Taubkin Splenic functions have been studied in children with sickle cell anemia by determination of 99 Tcm uptake and release of factor VIII after adrenaline infusion. A significant correlation between early cessation...
Journal Articles
Benign Sickle Cell Anemia in Israeli-Arabs with High Red Cell 2,3 Diphosphoglycerate
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1978) 59 (4): 237–245.
Published Online: 03 March 2009
... to in the content or advertisements. Sickle cell anemia Hemoglobin S 2,3 Diphosphoglycerate Acta haemat. 59: 237-245 (1978) Benign Sickle Cell Anemia in Israeli-Arabs with High Red Cell 2,3 Diphosphoglycerate E ugene F. R oth, jr., E liezer H. R achmilewitz, Alicia Schifter and R onald L. N agel Division...
Journal Articles
111 In Chloride Bone Marrow Scintigraphy and Ferrokinetic Studies in a Case of Sickle Cell Anemia with Transient Erythroid Aplasia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1979) 61 (6): 330–333.
Published Online: 03 March 2009
...Richard E. Helmer III; Bettye A. Sayle; Jack B. Alperin; Frank H. Gardner A patient with sickle cell anemia was hospitalized because of an acute erythropoietic aplastic crisis. 111 In chloride bone marrow scintigraphy performed during the aplastic crisis showed markedly impaired uptake...
Journal Articles
Circulating Immune Complexes in Sickle Cell Hepatic Crises
Available to PurchaseP. Hernández, J. Carnot, C. Cruz, E. Dorticós, E. Espinosa, A. Gonzáles, M.N. Santos, R. Villaescusa
Journal:
Acta Haematologica
Acta Haematol (1981) 65 (1): 15–20.
Published Online: 27 February 2009
...P. Hernández; J. Carnot; C. Cruz; E. Dorticós; E. Espinosa; A. Gonzáles; M.N. Santos; R. Villaescusa Circulating immune complexes in sera from sickle cell anemia (SCA) patients were investigated using inhibition of complement-dependent lymphocyte rosette formation (EAC rosette inhibition...
Journal Articles
Zinc and Copper Status in Patients with Sickle Cell Anemia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1987) 77 (2): 87–89.
Published Online: 25 February 2009
...A.I. Alayash; A. Dafallah; A.A. Al-Quorain; A.H.S. Omer; M.T. Wilson Plasma zinc and copper concentrations were determined by atomic absorption spectroscopy in 57 patients with sickle cell anemia and in 45 control subjects from the Eastern Province of Saudi Arabia. Plasma zinc and copper levels...
Journal Articles
Priapism in Association with Sickle Cell Anemia in Saudi Arabia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1985) 73 (3): 181–182.
Published Online: 25 February 2009
...Baker Al-Awamy; Saud A. Taha; Mahtab A. Naeem A questionnaire study of 42 Saudi patients with sickle cell anemia revealed that none of them had ever suffered from priapism. A comparison of hematological parameters between Jamaican priapism patients and Saudi non-priapism patients suggested...
Journal Articles
Erythrocyte Density Distribution in Sickle Cell Anemia
Available to Purchase
Journal:
Acta Haematologica
Acta Haematol (1984) 71 (6): 361–370.
Published Online: 25 February 2009
... advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Red cell density Sickle cell anemia...
Journal Articles
Glycosylated Hemoglobin Levels in a Benign Form of Sickle Cell Anemia in Saudi Arabia
Available to PurchaseA.I. Alayash, A. Dafallah, H. Al-Husayni, A.K. Al-Ali, A. Al-Quorain, A.H.S. Omer, M.T. Wilson, J. Bonaventura, R. Cashon
Journal:
Acta Haematologica
Acta Haematol (1986) 75 (3): 160–164.
Published Online: 25 February 2009
...A.I. Alayash; A. Dafallah; H. Al-Husayni; A.K. Al-Ali; A. Al-Quorain; A.H.S. Omer; M.T. Wilson; J. Bonaventura; R. Cashon Glycosylated hemoglobin was determined by the thiobarbituric acid method in sickle cell anemia patients from the Eastern Province of Saudi Arabia. The level of glycosylated...
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