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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 1
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Original Article

β-Thalassemia in Yugoslavia

A. Dimovski Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
D. G. Efremov Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
L. Jankovic Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
G. D. Efremov Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
D. Juricic Department of Clinical Chemistry, University Hospital Dr. 0. Novosel, 41000, Zagreb, Yugoslavia
,
N. Zisovski Department of Pediatrics, Faculty of Medicine, 91000, Skopje, Yugoslavia
,
N. Stojanovski Medical Center Titov Veles, 93000, Titov Veles, Yugoslavia
,
N. Nikolov Medical Center Strumica, 92000, Strumica, Yugoslavia
,
G. T. Petkov Medical Center Gevgelija, 93000, Gevgelija, Yugoslavia
,
A. L. Reese Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
T. A. Stoming Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H. J. Huisman Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
 show all
Pages 15-24 | Received 01 Dec 1989, Accepted 18 Jan 1990, Published online: 07 Jul 2009

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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Georgi D. Efremov. (2007) Thalassemias and Other Hemoglobinopathies in the Republic of Macedonia. Hemoglobin 31:1, pages 1-15.
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Mahmoud Abd El-Latif, Dvora Filon, Deborah Rund, Ariella Oppenheim & Moien Kanaan. (2002) THE β+-IVS-I-6 (T → C) MUTATION ACCOUNTS FOR HALF OF THE THALASSEMIA CHROMOSOMES IN THE PALESTINIAN POPULATIONS OF THE MOUNTAIN REGIONS. Hemoglobin 26:1, pages 33-40.
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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S. N. Khan, S. Riazuddin & R. Galanello. (2000) Identification of Three Rare β-Thalassemia Mutations in the Pakistani Population. Hemoglobin 24:1, pages 15-22.
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Güngor Nişli, Kaan Kavakli, Yeşim Aydinok, Senay Oztop & Nazan Cetingül. (1997) Beta-Thalassemia Alleles in Aegean Region of Turkey: Effect on Clinical Severity of Disease. Pediatric Hematology and Oncology 14:1, pages 59-65.
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L. Stefanis, E. Kanavakis, J. Traeger-Synodinos, M. Tzetis, A. Metaxotou-Mavromati & C. Kattamis. (1994) Hematologic Phenotype of the Mutations Ivs1-n6 (T →. C), lVS1-n110 (C → A), AND CD39 (C → T) IN CARRIERS OF P-THALASSEMIA IN GREECE. Pediatric Hematology and Oncology 11:5, pages 509-517.
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M. R. Noori-Daloii, N. Moazami, S. Farhangi, A. Atalay, I. N. Geren, L. Akar, E. O. Atalay, B. Clirakoglu & E. Bermek. (1994) β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm. Hemoglobin 18:6, pages 449-453.
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L. Jankovic, A. J. Dimovski, G. D. Efremov & D. Juricic. (1992) A Mutation at CDS 82/83 (-G) Observed in a Yugoslavian Family with a Heterozygosity for β-Thalassemia. Hemoglobin 16:4, pages 291-294.
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G. D. Efremov. (1992) Special Feature Hemoglobinopathies in Yugoslavia: an Update. Hemoglobin 16:6, pages 531-544.
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R. Öner, S. Agarwal, A. J. Dimovski, G. D. Efremov, G. H. Petkov, C. Altay, A. Gurgey & T. H.J. Huisman. (1991) The G→A Mutation at Position +22 31 to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia. Hemoglobin 15:1-2, pages 67-76.
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S. Fattoum, F. Guemira, C. Öner, R. Öner, H-W. Li, F. Kutlar & T. H.J. Huisman. (1991) β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians. Hemoglobin 15:1-2, pages 11-21.
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Articles from other publishers (18)

Nikolaos Sousos, Despoina Adamidou, Philippos Klonizakis, Alexandra Agapidou, Stamatia Theodoridou, Georgios Spanos, Kyriakos Psarras, Evaggelia Vetsiou, Timoleon-Achilleas Vyzantiadis & Efthymia Vlachaki. (2017) Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence. Acta Haematologica 137:3, pages 175-182.
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Biljana Atanasovska, Georgi Bozhinovski, Dijana Plaseska-Karanfilska & Lyubomira Chakalova. (2012) Efficient Detection of Mediterranean β-Thalassemia Mutations by Multiplex Single-Nucleotide Primer Extension. PLoS ONE 7:10, pages e48167.
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Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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G Efremov. (2008) Thalassemias and Other Hemoglobinopathies in Former Yugoslavia. Balkan Journal of Medical Genetics 11:1, pages 11-26.
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Shahina Daar, David Gravell, Hussein M. Hussein, Anil V. Pathare, Yasser Wali & Rajagopal Krishnamoorthy. (2007) Haematological and clinical features of β-thalassaemia associated with Hb Dhofar. European Journal of Haematology 80:1, pages 67-70.
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N. J. Makhoul, R. S. Wells, H. Kaspar, H. Shbaklo, A. Taher, N. Chakar & P. A. Zalloua. (2005) Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration. Annals of Human Genetics 69:1, pages 55-66.
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M.F. Sadiq, A. Eigel & J. Horst. (2001) Spectrum of β‐thalassemia in Jordan: Identification of two novel mutations. American Journal of Hematology 68:1, pages 16-22.
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G.O. Tadmouri, Ş. Tüzmen, H. Özçelik, A. Özer, S.M. Baig, E.B. Senga & A.N. Başak. (1998) Molecular and population genetic analyses of β-Thalassemia in Turkey. American Journal of Hematology 57:3, pages 215-220.
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Gino Schilirò, Elena Mirabile, Rosario Testa, Giovanna Russo-Mancuso & Salvatore P. Dibenedetto. (1997) Presence of hemoglobinopathies in Sicily: A historic perspective. American Journal of Medical Genetics 69:2, pages 200-206.
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G. Schilirò, F. di Gregorio, P. Samperi, E. Mirabile, R. Liang, M. A. Cürük, Z. Ye & T. H. J. Huisman. (2006) Genetic heterogeneity of β‐thalassemia in southeast sicily. American Journal of Hematology 48:1, pages 5-11.
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D. G. Efremov, A. J. Dimovski, E. Sukarova, G. Schiliro, N. Zisovski, G. D. Efremov, O. R. Burrone & T. H. J. Huisman. (1994) γ-mRNA and Hb F levels in β-thalassaemia. British Journal of Haematology 88:2, pages 311-317.
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D. G. Efremov, A. J. Dimovski, E. Baysal, Z. Ye, A. D. Adekile, M. L. S. Ribeiro, G. Schiliro, Ç. Altay, A. Gürgey, G. D. Efremov & T. H. J. Huisman. (2008) Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation. British Journal of Haematology 86:4, pages 824-830.
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A. J. Dimovski, A. D. Adekile, V. Divoky, E. Baysal & T. H. J. Huisman. (2006) Polymorphic pattern of the (AT) x (T) y motif at −530 5′ to the β‐globin gene in over 40 patients homozygous for various β‐thalassemia mutations . American Journal of Hematology 45:1, pages 51-57.
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Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1993) 8 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 6:1, pages 215-262.
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G. Schiliro'P. Samperi, R. Testa, R. B. Gupta, L.‐H. Gu & T. H. J. Huisman. (2006) Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia. American Journal of Hematology 41:4, pages 264-269.
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A. N. Başak, H. Özçelik, A. Özer, A. Tolun, M. Aksoy, L. Ağaoğlu, F. Ridolfi, L. Ulukutlu, N. Akar, A. Gürgey & B. Kirdar. (1992) The molecular basis of β-thalassemia in Turkey. Human Genetics 89:3, pages 315-318.
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A. E. Kulozik. (1992) β-thalassaemia: Molecular pathogenesis and clinical variability. European Journal of Pediatrics 151:2, pages 78-84.
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T. H. J. Huisman. (2008) FREQUENCIES OF COMMON β ‐THALASSAEMIA ALLELES AMONG DIFFERENT POPULATIONS: VARIABILITY IN CLINICAL SEVERITY . British Journal of Haematology 75:4, pages 454-457.
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