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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 6
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Original Article

Special Feature Hemoglobinopathies in Yugoslavia: an Update

Pages 531-544 | Received 19 Mar 1992, Accepted 01 Sep 1992, Published online: 07 Jul 2009

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Read on this site (3)

Laudy Cherry, Carla Calo, Rodica Talmaci, Pascale Perrin & Lucian Gavrila. (2016) β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area. Hemoglobin 40:2, pages 85-96.
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Milena Radmilovic, Branka Zukic, Biljana Stankovic, Teodora Karan-Djurasevic, Maja Stojiljkovic, Vesna Spasovski, Natasa Tosic, Lidija Dokmanovic, Dragana Janic & Sonja Pavlovic. (2010) Thalassemia Syndromes in Serbia: An update. Hemoglobin 34:5, pages 477-485.
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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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Articles from other publishers (18)

Giovanna De Simone, Alberto Quattrocchi, Benedetta Mancini, Alessandra di Masi, Clara Nervi & Paolo Ascenzi. (2022) Thalassemias: from gene to therapy. Molecular Aspects of Medicine 84, pages 101028.
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Ambarkova Vesna, Krmzova Tina & Nonkulovski Zoran. (2021) Thalassemia-Beta major-Case report. Archives of Hematology Case Reports and Reviews, pages 021-025.
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Audrey D. Kamzan, Charles A. Newcomer, Laura J. Wozniak, Noah C. Federman & Lydia S. Kim. (2020) A Case of a 15-Month-Old With Periorbital Edema and Severe Anemia. Pediatrics 145:3.
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Andrea Tesija Kuna, Kristina Dukic, Nora Nikolac Gabaj, Marijana Miler, Ines Vukasovic, Sanja Langer, Ana-Maria Simundic & Nada Vrkic. (2018) Comparison of Enzymatic Assay for HBA1C Measurement (Abbott Architect) With Capillary Electrophoresis (Sebia Minicap Flex Piercing Analyser). Laboratory Medicine.
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Jerko Vucak, Daniel Turudic, Danko Milosevic, Marko Bilic, Zrinko Salek, Martina Rincic & Ernest Bilic. (2018) Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene Mutations. Journal of Pediatric Hematology/Oncology 40:2, pages e77-e82.
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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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W.-J. Cai, J. Li, X.-M. Xie & D.-Z. Li. (2015) Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F. International Journal of Laboratory Hematology 37:6, pages 752-757.
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Giuseppina Lacerra, Romeo Prezioso, Gennaro Musollino, Giulio Piluso, Lucia Mastrullo & Maria De Angioletti. (2013) Identification and molecular characterization of a novel 55‐kb deletion recurrent in southern Italy: the Italian G γ( A γδβ)°‐thalassemia . European Journal of Haematology 90:3, pages 214-219.
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Roberto H. Nussenzveig, Derek L. Vanhille, Dottie Hussey & Archana M. Agarwal. (2012) Development of a rapid multiplex PCR assay for identification of the three common Hemoglobin‐Lepore variants (Boston‐Washington, Baltimore, and Hollandia) and identification of a new Lepore variant. American Journal of Hematology 87:10.
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Mirko Spiroski. (2009) Déjà vu - A Report of Highly Similar Citations in the Biomedical Scientific Literature from the Republic of Macedonia. Macedonian Journal of Medical Sciences 2:2, pages 107-114.
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Sean M. McKeown, Harris Carmichael, Rhea-Beth Markowitz, Abdullah Kutlar, Leslie Holley & Ferdane Kutlar. (2008) Rare occurrence of Hb Lepore-Baltimore in African Americans: molecular characteristics and variations of Hb Lepores. Annals of Hematology 88:6, pages 545-548.
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Georgi D. Efremov. (2008) How I became a biochemist. IUBMB Life 60:7, pages 481-482.
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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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Maria De Angioletti, Giuseppina Lacerra, Leonilde Pagano, Mario Alessi, Rossana D'Avino, Laura Manca & Clementina Carestia. (2004) β -thalassaemia-87 C→G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients . British Journal of Haematology 126:5, pages 743-749.
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George P. Patrinos, Panagoula Kollia, Elisavet Papapanagiotou, Aphrodite Loutradi-Anagnostou, Dimitris Loukopoulos & Manoussos N. Papadakis. (2001) A?-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5? regulatory region of the human A?-globin gene. American Journal of Hematology 66:2, pages 99-104.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1998) 1 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 1-51.
Crossref
E. Mirabile, R. Testa, C. Consalvo, R. Dickerhoff & G. Schilirò. (2009) Association of Hb S/Hb lepore and δβ‐thalassemia/Hb lepore in Sicilian patients: Review of the presence of Hb lepore in Sicily. European Journal of Haematology 55:2, pages 126-130.
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