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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 4
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Original Article

Determinants of Red Cell Survival and Erythropoietic Activity in Patients with Sickle Cell Anemia in the Steady State

S. K. Ballas Department of Medicine Jefferson Medical College, Cardeza Foundation for Hematologic Research, Philadelphia, PA, 19107, USACorrespondence[email protected]
&
M. J. Marcolina Department of Medicine Jefferson Medical College, Cardeza Foundation for Hematologic Research, Philadelphia, PA, 19107, USA
Pages 277-286 | Received 27 Mar 2000, Accepted 30 May 2000, Published online: 07 Jul 2009

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Mentewab Ayalew, Derrick Hylton, Jeticia Sistrunk, James Melton, Kiandra Johnson & Eberhard Voit. (2022) Integration of Biology, Mathematics and Computing in the Classroom Through the Creation and Repeated Use of Transdisciplinary Modules. PRIMUS 32:3, pages 367-385.
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Taner Arpaci. (2018) Arrested pneumatization of the sphenoid sinus mimicking skull base tumours: MRI prevalence in children with haematologic diseases. International Journal of Neuroscience 128:11, pages 1040-1043.
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Articles from other publishers (15)

Justin K. Kirkham, Jeremie H. Estepp, Mitch J. Weiss & Sara R. Rashkin. (2023) Genetic Variation and Sickle Cell Disease Severity. JAMA Network Open 6:10, pages e2337484.
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Nesma Ahmed Safwat, Mai Mohamed ELkhamisy, Soha Ezz AlArab Abdel-Wahab, Mohamed Tarif Hamza, Noha Hussein Boshnak & Mahmoud Adel Kenny. (2020) Polymorphisms of the receptor for advanced glycation end products as vasculopathy predictor in sickle cell disease. Pediatric Research 89:1, pages 185-190.
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Francisco A. Ferreira, Bruno D. Benites, Fernando F. Costa, Simone Gilli & Sara T. Olalla-Saad. (2019) Recombinant erythropoietin as alternative to red cell transfusion in sickle cell disease. Vox Sanguinis 114:2, pages 178-181.
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Nesma Ahmed Safwat & Mahmoud Adel Kenny. (2018) Soluble receptor for advanced glycation end products as a vasculopathy biomarker in sickle cell disease. Pediatric Research 84:6, pages 869-874.
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Shahida A. Khan, Ghazi Damanhouri, Ashraf Ali, Sarah A. Khan, Aziz Khan, Ahmed Bakillah, Samy Marouf, Ghazi Al Harbi, Saeed H. Halawani & Ahmad Makki. (2016) Precipitating factors and targeted therapies in combating the perils of sickle cell disease--- A special nutritional consideration. Nutrition & Metabolism 13:1.
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A.V. Prabhu & B.F. BranstetterIVIV. (2016) The CT Prevalence of Arrested Pneumatization of the Sphenoid Sinus in Patients with Sickle Cell Disease. American Journal of Neuroradiology 37:10, pages 1916-1919.
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Amira A. Adly, Eman A. Ismail, Nevine G. Andrawes, Mai M. Mahmoud & Rasha Eladawy. (2016) Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease. Cytokine 79, pages 52-58.
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Clarisse Lopes de Castro Lobo, Emilia Matos do Nascimento, Renato Abelha, Ana Maria Mach Queiroz, Philippe Connes, Gilberto Perez Cardoso & Samir K. Ballas. (2015) Risk Factors of Pulmonary Hypertension in Brazilian Patients with Sickle Cell Anemia. PLOS ONE 10:9, pages e0137539.
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Samir K. Ballas. (2015) Clinical Utility of Lactate Dehydrogenase in Determining the Severity of Hemolysis in Sickle Cell Anemia. American Journal of Clinical Pathology 144:1, pages 173-174.
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Azza Abdel Gawad Tantawy, Amira Abdel Moneam Adly, Eman Abdel Rahman Ismail, Yasser Wagih Darwish & Marwa Ali Zedan. (2014) Growth differentiation factor-15 in young sickle cell disease patients: Relation to hemolysis, iron overload and vascular complications. Blood Cells, Molecules, and Diseases 53:4, pages 189-193.
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Claire C. Sharpe & Swee L. Thein. (2011) Sickle cell nephropathy – a practical approach. British Journal of Haematology 155:3, pages 287-297.
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Gail Dallalio & Robert T. MeansJr.Jr.. (2008) Placental growth factor attenuates suppression of erythroid colony formation by interferon. Translational Research 152:5, pages 233-238.
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Mamta Sharma, Manju R Mamtani, Manik Amin, Tushar P Thakre, Smita Sharma, Amit Amin & Hemant Kulkarni. (2006) Insights into age- and sickle-cell-disease- interaction using principal components analysis. BMC Hematology 6:1.
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Samir K. Ballas & Mary Jane Marcolina. (2006) Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia. Transfusion 46:1, pages 105-110.
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Vikki G. NolanDiego F. WyszynskiLindsay A. FarrerMartin H. Steinberg. (2005) Hemolysis-associated priapism in sickle cell disease. Blood 106:9, pages 3264-3267.
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