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Keywords: Sickle cell anemia
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Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2020) 143 (2): 163–175.
Published Online: 15 July 2019
... cell anemia Sickle cell disease Quality of life Transition Outcomes Pediatrics Adult Survey Sickle cell disease (SCD) is an inherited blood disorder affecting approximately 100,000 people of African, Mediterranean, and Asian descent in the USA [ 1 ]. Previously a disease of childhood...
Journal Articles
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2014) 132 (3-4): 340–347.
Published Online: 10 September 2014
... to in the content or advertisements. 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
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2011) 127 (1): 50–55.
Published Online: 25 October 2011
..., instructions or products referred to in the content or advertisements. Hemoglobin Sickle cell anemia Thalassemia When an African male complaining of thoracic pain presented at our hospital 13 years ago, we could easily have overlooked our first encounter with sickle cell anemia if we had...
Journal Articles
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
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
Subject Area:
Hematology , Oncology
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
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
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
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1987) 78 (1): 54–56.
Published Online: 25 February 2009
... in patients with sickle cell anemia when compared with those SS subjects with G-6-PD deficiency. Since glycosylated Hb is considered as an index of the red blood cell’s life span, it is suggested that the enzyme defect in these patients is possibly ameliorating the severity of sickle cell anemia Actahaemat...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1984) 71 (6): 361–370.
Published Online: 25 February 2009
... disorders and displays the profile of erythrocyte density heterogeneity for the individual sickle cell patient. Red cell density Sickle cell anemia Original Papers Actahaemat. 71: 361-370(1984) Erythrocyte Density Distribution in Sickle Cell Anemia Henri B. Weems, Lawrence S. Lessin Division...
Journal Articles
Subject Area:
Hematology , Oncology
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
Subject Area:
Hematology , Oncology
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...