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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 1
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Original

Thalassemias and Other Hemoglobinopathies in the Republic of Macedonia

Pages 1-15 | Received 04 Aug 2006, Accepted 11 Sep 2006, Published online: 07 Jul 2009

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Read on this site (6)

Marija Dimishkovska, Maja Kuzmanovska, Svetlana Kocheva, Kata Martinova, Oliver Karanfilski, Zlate Stojanoski & Dijana Plaseska-Karanfilska. (2017) First Cases of Hb Agrinio Described in Patients from the Republic of Macedonia. Hemoglobin 41:4-6, pages 308-310.
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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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Biyan Chen, Peng Huang, Shang Yi, Qiuli Chen, Yanqing Tang, Qiang Zhang & Sheng He. (2015) First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family. Hemoglobin 39:3, pages 207-208.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Ayfer Atalay, Hasan Koyuncu, Aylin Köseler, Anzel Ozkan & Erol Ö. Atalay. (2007) Hb Beograd [β121(GH4)Glu→Val, GAA→GTA] in the Turkish Population. Hemoglobin 31:4, pages 491-493.
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Articles from other publishers (13)

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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Adivitch Sripusanapan, Arunee Phusua, Kanda Fanhchaksai & Pimlak Charoenkwan. (2020) Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region ( HBB : c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia . Pediatric Blood & Cancer 67:4.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
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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Nejat Mahdieh & Bahareh Rabbani. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews 30:6, pages 493-508.
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Velibor Tasic, Dragan Danilovski & Zoran Gucev. (2016) The Child Health Care System of Macedonia. The Journal of Pediatrics 177, pages S127-S137.
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Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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H López‐Escribano, MM Parera, P Guix, JM Serra, A Gutierrez, D Balsells, E Oliva‐Berini, JA Castro, MM Ramon & A Picornell. (2012) Balearic archipelago: three islands, three beta‐thalassemia population patterns. Clinical Genetics 83:2, pages 175-180.
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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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Antonino Giambona, Margherita Vinciguerra, Monica Cannata, Filippo Cassarà, Germana Fiorentino, Filippo Leto, Pina Lo Gioco, Disma Renda, Cristina Passarello & Aurelio Maggio. (2011) The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island. Blood Cells, Molecules, and Diseases 46:4, pages 282-287.
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A Babameto-Laku, A Mitre, S Berisha, V Mokini & D Roko. (2011) Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population. Balkan Journal of Medical Genetics 14:1, pages 45-50.
Crossref
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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Georgi D. Efremov. (2008) How I became a biochemist. IUBMB Life 60:7, pages 481-482.
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