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Case Reports in Genetics
Volume 2012 (2012), Article ID 136582, 3 pages
Sickle Retinopathy in a Person with Hemoglobin S/New York Disease
1Department of Surgery, Radiology, Anaesthetics, and Intensive Care, Faculty of Medical Sciences, University of the West Indies, Mona, Kingston 7, Jamaica
2Universite des Antilles et de la Guyane, Centre Hospitalier Universitaire (CHU), Pointe-a-Pitre, UMR S 458 Inserm, 97159 Guadeloupe, France
3Inserm U763, Pointe-à-Pitre, 97159 Guadeloupe, France
4Université des Antilles et de la Guyane, 97159 Guadeloupe, France
5Sickle Cell Unit, Tropical Medicine Research Institute, University of the West Indies, Mona, Kingston 7, Jamaica
Received 30 November 2012; Accepted 19 December 2012
Academic Editors: S. Chappell and M. Velinov
Copyright © 2012 Donovan Calder et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- Z. Yi-Tao and H. Shu-Zheng, “Hemoglobin New York (α2β2 113(G15) VAL → GLU) in China,” Hemoglobin, vol. 6, no. 1, pp. 61–67, 1982.
- R. Q. Blackwell, C. S. Liu, and C. L. Wang, “Hemoglobin New York in Chinese subjects in Taiwan,” American Journal of Physical Anthropology, vol. 34, no. 3, pp. 329–334, 1971.
- S. Pootrakul, S. Wasi, S. NaNakorn, and G. H. Dixon, “Double heterozygosity for hemoglobin E and hemoglobin New York in a Thai family,” Journal of the Medical Association of Thailand, vol. 54, no. 10, pp. 688–697, 1971.
- T. Harano, K. Harano, S. Ueda, S. Shibata, K. Imai, Y. Ohba, et al., “Hemoglobin New York [β113 (G 15) Val → Glu] found in a Japanese female with cholelithiasis. Its structure, function, instability and biosynthesis,” Hemoglobin, vol. 6, no. 6, pp. 619–624, 1982.
- G. F. Saenz, J. Elizondo, and G. Arroyo, “Two cases of hemoglobin New York in Costa Rica,” Hemoglobin, vol. 4, no. 1, pp. 101–105, 1980.
- V. Chan, T. K. Chan, S. C. Tso, and D. Todd, “Combination of three α-globin gene loci deletions and hemoglobin New York results in a severe hemoglobin H syndrome,” American Journal of Hematology, vol. 24, no. 3, pp. 301–306, 1987.
- A. McFarlane, T. E. Warkentin, and W. Cartin, “A novel sickling hemoglobinopathy,” The New England Journal of Medicine, vol. 365, no. 16, pp. 1548–1549, 2011.
- A. Joutovsky, J. Hadzi-Nesic, and M. A. Nardi, “HPLC retention time as a diagnostic tool for hemoglobin variants and hemoglobinopathies: a study of 60 000 samples in a clinical diagnostic laboratory,” Clinical Chemistry, vol. 50, no. 10, pp. 1736–1747, 2004.
- J. Sugihara, T. Imamura, T. Imoto, and T. Yanase, “Identification of an abnormal hemoglobin with reduced oxygen affinity by high-performance liquid chromatography,” Biochimica et Biophysica Acta, vol. 669, no. 1, pp. 105–108, 1981.
- J. Nia, W. C. Lam, D. M. Kleinman, M. Kirby, E. S. Liu, and K. T. Eng, “Retinopathy in sickle cell trait: does it exist?” Canadian Journal of Ophthalmology, vol. 38, no. 1, pp. 46–51, 2003.