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Hemoglobin
international journal for hemoglobin research
Volume 9, 1985 - Issue 6
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Original Article

Hematological Observations on Arabian SS Patients with a Homozygosity or Heterozygosity for a βS Chromosome with Haplotype #31

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Pages 545-557 | Received 15 Aug 1985, Accepted 10 Sep 1985, Published online: 07 Jul 2009

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Maureen M Okam & Benjamin L Ebert. (2012) Novel approaches to the treatment of sickle cell disease: the potential of histone deacetylase inhibitors. Expert Review of Hematology 5:3, pages 303-311.
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Amy E. Vinson, Aisha Walker, Dedrey Elam, Michele Glendenning, Ferdane Kutlar, Betsy Clair, Jeanette Harbin & Abdullah Kutlar. (2004) A Novel Approach to Rapid Determination of βS‐Globin Haplotypes: Sequencing of the Aγ‐IVS‐II Region. Hemoglobin 28:4, pages 317-323.
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Yih-Ming Yang & Betty Pace. (2001) Pharmacologic Induction of Fetal Hemoglobin Synthesis: Cellular and Molecular Mechanisms. Pediatric Pathology & Molecular Medicine 20:1, pages 87-106.
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M. H. Steinberg. (1996) Modulation of the Phenotypic Diversity of Sickle Cell Anemia. Hemoglobin 20:1, pages 1-19.
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S. Abbes, S. Fattoun, N. Vidaud, M. Goossens & J. Rosa. (1991) Sickle Cell Anemia in the Tunisian Population: Haplotyping and HB F Expression. Hemoglobin 15:1-2, pages 1-9.
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Luan Eng Lie-Injo, Mu Lan Lim, Zafar Randhawa, T. Vijayasilan & Khalid Hassan. (1987) Elevated Gγ Gene Expression with Specific βs Gene Haplotype, Normal γ Gene Maps and Presence of the Xmn I site -158 5′ to the Gγ Gene in Indian Sickle Cell Anemia. Hemoglobin 11:3, pages 231-239.
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Y. Hattori, F. Kutlar, A. Kutlar, V. C. McKie & T. H. J. Huisman. (1986) Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia. Hemoglobin 10:6, pages 623-642.
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Articles from other publishers (21)

Graham R. Serjeant & Elliott Vichinsky. (2018) Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors. Blood Cells, Molecules, and Diseases 70, pages 66-77.
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Li Liu, Alexander Pertsemlidis, Liang-Hao Ding, Michael D Story, Martin H Steinberg, Paola Sebastiani, Carolyn Hoppe, Samir K Ballas & Betty S Pace. (2016) Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. Experimental Biology and Medicine 241:7, pages 706-718.
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Steven R Goodman, Betty S Pace, Kirk C Hansen, Angelo D’alessandro, Yang Xia, Ovidiu Daescu & Stephen J Glatt. (2016) Minireview: Multiomic candidate biomarkers for clinical manifestations of sickle cell severity: Early steps to precision medicine. Experimental Biology and Medicine 241:7, pages 772-781.
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Betty S. Pace & Sima Zein. (2006) Understanding mechanisms of γ‐globin gene regulation to develop strategies for pharmacological fetal hemoglobin induction. Developmental Dynamics 235:7, pages 1727-1737.
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Abdulsalam Al-Sulaiman, Olajide Bademosi, Hassan Ismail & Gadi Magboll. (2016) Stroke in Saudi Children. Journal of Child Neurology 14:5, pages 295-298.
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A.D. Adekile, M. Tuli, M.Z. Haider, K. Al-Zaabi, S. Mohannadi & A. Owunwanne. (1996) Influence of α-thalassemia trait on spleen function in sickle cell anemia patients with high HbF. American Journal of Hematology 53:1, pages 1-5.
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M. H. Steinberg, H. Hsu, R. L. Nagel, P. F. Milner, J. G. Adams, L. Benjamin, S. Fryd, P. Gillette, J. Gilman, O. Josifovska, S. Hellman‐Erlingsson, S. Safaya, L. Huey & R. F. Rieder. (2006) Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia. American Journal of Hematology 48:3, pages 175-181.
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Kabita Bhaumik. (2006) Fetal hemoglobin synthesis in sickle cell anemia: Some molecular considerations. American Journal of Hematology 46:2, pages 101-106.
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A. D. Adekile & T. H. J. Huisman. (1993) Hb F in sickle cell anemia. Experientia 49:1, pages 16-27.
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Cihan �ner, AleksandarJ. Dimovski, NancyF. Olivieri, Gino Schiliro, JohnF. Codrington, Sladdehine Fattoum, AdekunleD. Adekile, Reyhan �ner, GunesT. Y�regir, C. Altay, A. Gurgey, RashikB. Gupta, VinodB. Jogessar, MichaelN. Kitundu, Dimitris Loukopoulos, GabrielP. Tamagnini, M.LeticiaS. Ribeiro, Ferdane Kutlar, Li-Hao Gu, KennethD. Lanclos & TitusH.J. Huisman. (1992) ?s Haplotypes in various world populations. Human Genetics 89:1, pages 99-104.
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Darleen R. Powars. (1991) ß s -Gene-Cluster Haplotypes in Sickle Cell Anemia: Clinical and Hematologic Features. Hematology/Oncology Clinics of North America 5:3, pages 475-493.
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R. F. Rieder, S. Safaya, P. Gillette, S. Fryd, H. Hsu, J. G. AdamsIIIIII & M. H. Steinberg. (2006) Effect of β‐Globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia. American Journal of Hematology 36:3, pages 184-189.
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Graham R. Serjeant. (1990) The Challenge of Sickle Cell Disease in Saudi Arabia. Annals of Saudi Medicine 10:4, pages 443-448.
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A. G. Falusi & A. E. Kulozik. (2009) Relationship of foetal haemoglobin levels and β s haplotypes in homozygous sickle cell disease . European Journal of Haematology 45:1, pages 1-4.
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G. R. SERJEANT. (1989) Geography and the Clinical Picture of Sickle Cell Disease.. Annals of the New York Academy of Sciences 565:1 Sickle Cell D, pages 109-119.
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Ferdane Kutlar, Jose M. Gonzalez-Redondo, Abdullah Kutlar, Aytemiz Gurgey, �igdem Altay, Georgi D. Efremov, Klara Kleman & Titus H. J. Huisman. (1989) The levels of ?, ?, and ? chains in patients with Hb H disease. Human Genetics 82:2, pages 179-186.
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Frank B. Livingstone. (2005) Who gave whom hemoglobin S: The use of restriction site haplotype variation for the interpretation of the evolution of the β S ‐globin gene . American Journal of Human Biology 1:3, pages 289-302.
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S.K. Joishy, K. Hassan, M. Lopes & L.E. Lie-Injo. (1988) Clinical, genetic and fertility studies of Indians with βS-globin gene and the influence of Hb S on Plasmodium falciparum malaria infection. Transactions of the Royal Society of Tropical Medicine and Hygiene 82:4, pages 515-519.
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G. D. Efremov, I. Gjorgovski, N. Stojanovski, J. C. Diaz-Chico, T. Harano, F. Kutlar & T. H. J. Huisman. (1987) One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population. Human Genetics 77:2, pages 132-136.
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P. J. Ojwang, T. Ogada, P. Beris, Y. Hattori, K. D. Lanclos, A. Kutlar, F. Kutlar & T. H. J. Huisman. (2008) Haplotypes and α globin gene analyses in sickle cell anaemia patients from Kenya. British Journal of Haematology 65:2, pages 211-215.
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Barbara A. Miller, Nancy Olivieri, Mohammed Salameh, Mohammed Ahmed, Giovanna Antognetti, Titus H.J. Huisman, David G. Nathan & Stuart H. Orkin. (1987) Molecular Analysis of the High-Hemoglobin-F Phenotype in Saudi Arabian Sickle Cell Anemia. New England Journal of Medicine 316:5, pages 244-250.
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