Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in Greece
1962; Wiley; Volume: 8; Issue: 1 Linguagem: Inglês
10.1111/j.1365-2141.1962.tb06489.x
ISSN1365-2141
AutoresB. Malamos, P Fessas, G. Stamatoyannopoulos,
Tópico(s)Archaeology and Historical Studies
ResumoBritish Journal of HaematologyVolume 8, Issue 1 p. 5-14 Types of Thalassaemia-Trait Carriers as Revealed by a Study of their Incidence in Greece B. Malamos, B. Malamos Department of Clinical Therapeutics, University of Athens *Search for more papers by this authorPh. Fessas, Ph. Fessas Department of Clinical Therapeutics, University of Athens *Search for more papers by this authorG. Stamatoyannopoulos, G. Stamatoyannopoulos Department of Clinical Therapeutics, University of Athens *Search for more papers by this author B. Malamos, B. Malamos Department of Clinical Therapeutics, University of Athens *Search for more papers by this authorPh. Fessas, Ph. Fessas Department of Clinical Therapeutics, University of Athens *Search for more papers by this authorG. Stamatoyannopoulos, G. Stamatoyannopoulos Department of Clinical Therapeutics, University of Athens *Search for more papers by this author First published: January 1962 https://doi.org/10.1111/j.1365-2141.1962.tb06489.xCitations: 85 Postal address: Vars. Sophias and K. Lourou St., Athens 6, Greece AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Ager, J. A. M. and Lehmann, H. (1958). ‘Observations on some “fast” haemoglobins: K, J, N, and “Bart's. Brit. med. J., i, 929. 10.1136/bmj.1.5076.929 CASWeb of Science®Google Scholar Bianco, I., Montalenti, G., Silvestroni, E. and Siniscalco, M. (1952). ‘Further data on genetics of microcythaemia or thalassaemia minor and Cooley's disease or thalassaemia major. Ann. Eugen. (Carnb.), 16, 299. 10.1111/j.1469-1809.1951.tb02483.x CASPubMedWeb of Science®Google Scholar Brecher, G., Schneiderman, M. and Williams, G. Z. (1956). ‘Evaluation of electronic red cell counter. Amer. J. clin. Path., 26, 1439. 10.1093/ajcp/26.12.1439 CASPubMedWeb of Science®Google Scholar Callender, S. T., Mallett, B. J. and Lehmann, H. (1961). ‘Thalassaemia in Britain. Brit. J. Haemat., 7, 1. 10.1111/j.1365-2141.1961.tb00314.x CASPubMedWeb of Science®Google Scholar Caminopetros, J. (1937). ‘The erythroblastic anaemia of the populations of the eastern Mediterranean. Public. Acad. Athens, vol. 6, No. 3, Athens . Google Scholar Carcassi, U., Ceppellini, R. and Pitzus, F. (1957). ‘Fre-quenza della talassemia in quatro popolazioni sarde e suoi rapporti con la distribuzione dei gruppi sanguigni e della malaria. Boll. 1st. sieroter. milan., 36, 206. CASPubMedGoogle Scholar Carcassi, U., Ceppellini, R. and Siniscalco, M. (1957). ‘II tracciato elettroforetico dell'emoglobina per una migliore discriminazione delle talassemie. Haemntologica, 42, 1635. CASPubMedGoogle Scholar Chernoff, A. I. (1959). ‘The distribution of the Thalas-semia gene: a historical review. Blood, 14, 899. CASPubMedWeb of Science®Google Scholar Dacie, J. V. (1956). Practical Haematology. 2nd edn., Churchill, London , p. 94. Google Scholar Edington, G. M. and Lehmann, H. (1955). ‘Expression of the sickle-cell gene in Africa. Brit. med. J., ii, 1328. 10.1136/bmj.2.4951.1328 Google Scholar Fessas, Ph. (1959a). ‘Observations on a second haemoglobin abnormality in haemoglobin-H disease. Proc. 7th Congr. Europ. Soc. Haemat., London. Presentation No. 301 (in press). Google Scholar Fessas, Ph. (1959b). ‘Haemoglobin “Bart's. Brit. med. J., ii, 886. 10.1136/bmj.2.5156.886 Google Scholar Fessas, Ph. and Mastrokalos, N. (1959). ‘Demonstration of small components in red cell haernolysates by starchgel electrophoresis. Nature (Lond.), 183, 1261. 10.1038/1831261a0 CASPubMedWeb of Science®Google Scholar Fessas, Ph. and Papaspyrou, A. (1957). ‘New “fast” hemoglobin associated with thalassemia. Science, 126, 1119. 10.1126/science.126.3283.1119 CASPubMedWeb of Science®Google Scholar Fessas, Ph., Stamatoyannopoulos, G. and Karaklis, A. (January 1962). ‘Variant of haemoglobin in trait and disease resembling thalassaemia. Proc. med. Soc. Athens, 37, 361. Google Scholar Gerald, P. S. and Diamond, L. K. (1958). ‘A new hereditary hemoglobinopathy, (the Lepore trait) and its interaction with thalassemia trait. Blood, 13, 835. CASPubMedGoogle Scholar Goldberg, C. A. J. (1958). ‘A new method for starch-gel electrophoresis of human hemoglobin, with special reference to the determination of hemoglobin A2. Clin. Chem., 4, 484. CASPubMedWeb of Science®Google Scholar Gouttas, A., Fessas, Ph., Tsevrenis, H. and Xefteri, E. (1955). ‘Description d'une nouvelle variété d'anémie hémolytique congénitale. Sang, 26, 911. CASPubMedGoogle Scholar Herman, E. C., Jr. and Conley, C. L. (January 1962). ‘Hereditary persistence of fetal hemoglobin. Amer. J. Med., 29, 9. 10.1016/0002-9343(60)90003-6 PubMedWeb of Science®Google Scholar Huisman, T. H. J. (1939). ‘ The identification of human haemoglobins.’ J. H. P. Jonxis and J. F. Delafresnaye (ed.) Abnormal Hoemoglobins, p. 33. Blackwell Scientific Publications, Oxford . Google Scholar Hunt, J. A. and Lehmann, H. (1969). ‘Haemoglobin “Bart's”: a foetal haemoglobin without α-chains. Nature (Lond.), 184, 872. 10.1038/184872a0 CASPubMedGoogle Scholar Ingram, V. M. and Stretton, A. O. W. (1959). ‘Genetic basis of the thalassaemia diseases. Nature (Lond.), 184, 1903. 10.1038/1841903a0 CASPubMedWeb of Science®Google Scholar Jacob, G. F. and Raper, A. B. (1958) ‘Hereditary persistence of foetal haemoglobin production, and its interaction with the sickle-cell trait. Brit. J. Haemat., 4, 138. 10.1111/j.1365-2141.1958.tb03844.x CASPubMedWeb of Science®Google Scholar Jones, R. T., Schroeder, W. A., Balog, J. E. and Vinograd, J. R. (1959). ‘Gross structure of haemoglobin-H. J. Amer. chem. Soc., 81, 3161. 10.1021/ja01521a080 CASWeb of Science®Google Scholar Kunkel, H. G. and Wallenius, G. (1955). ‘New henioglobin in normal adult blood. Science, 122, 288. 10.1126/science.122.3163.288 CASPubMedWeb of Science®Google Scholar Lie-injo Luan Eng and Jo Bwan Hie (January 1962). ‘Hydrops foetalis with a fast-moving haemoglobin. Brit. med. J., ii, 1649. Google Scholar Olesen, E. B., Olesen, K., Livingstone, F. B., Cohen, F., Zuelzer, W. W., Robinson, A. R. and Neel, J. V. (1959) ‘Thalassaemia in Liberia. Brit. med. J., i, 1385. 10.1136/bmj.1.5134.1385 CASWeb of Science®Google Scholar Papaspyrou, A. (1959). ‘ Observations on the haemoglobin A2.’ M.D. Thesis, University of Athens. Google Scholar Silvestroni, E. and Bianco, I. (1957). ‘Sull'esistenza nella popolazione italiana di sogetti non microcitemici portatori di un'elevata quota di emoglobina adulta lenta (Hb A2). Policlinico, Sez. Prat., 64, 1868. CASPubMedGoogle Scholar Silvestroni, E. and Bianco, I. (1958). ‘Associazione di Hb Ge microcitemia in due membri di una famiglia italiana del Ferrarese. Policlinico, Sez. Prat., 65, 203. PubMedGoogle Scholar Silvestroni, E. and Bianco, I. (1959). ‘ The distribution of microcythaernias (or thalassaemias) in Italy.’ J. H. P. Jonxis and J. F. Delafresnaye (ed.). Abnormal Haemoglobins, p. 242. Blackwell Scientific Publications, Oxford . Google Scholar Singer, K., Chernoff, A. I. and Singer, L. (1951). ‘Studies on abnormal haemoglobins, I. Their demonstration in sickle-cell anemia and other hematologic disorders by means of alkali denaturation. Blood, 6, 413. CASPubMedWeb of Science®Google Scholar Siniscalco, M. and Smith, C. A. B. (1955). ‘ The discrimination between normals and microcythemics as a statistical problem. Proc. 5th Congr. int. Soc. Blood Transfusion. Google Scholar Went, L. N. and MacIver, J. E. (1958). ‘An unusual type of hemoglobinopathy resembling sickle-cell — thalasse mia disease in a Jamaican family. Blood, 13, 559. CASPubMedWeb of Science®Google Scholar Citing Literature Volume8, Issue1January 1962Pages 5-14 ReferencesRelatedInformation
Referência(s)