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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 3
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Original Article

Hb Bart's Levels in Cord Blood and α-Thalassemia Mutations in Cyprus

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Pages 171-180 | Received 08 Sep 1999, Accepted 08 Mar 2000, Published online: 07 Jul 2009

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Read on this site (8)

Ilham Youssry, Ayman El Badawy, Rania M. Samy, Niveen Salama, Dalia Abd Elaziz & Samia Rizk. (2018) Prevalence of α-Thalassemia in the Egyptian Population. Hemoglobin 42:4, pages 243-246.
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Andreani R. Kyrri, Xenia Felekis, Eleni Kalogerou, Barbara J. Wild, Loukas Kythreotis, Marios Phylactides & Marina Kleanthous. (2009) Hemoglobin Variants in Cyprus. Hemoglobin 33:2, pages 81-94.
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Mohammad T. Akbari, Pantea Izadi, Mina Izadyar, Kyriacou Kyriacou & Marina Kleanthous. (2008) Molecular Basis of Thalassemia Intermedia in Iran. Hemoglobin 32:5, pages 462-470.
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Xenia Felekis, Marios Phylactides, Anthi Drousiotou, Sotiroulla Christou, Andreani Kyrri, Kyriakos Kyriakou, Eleni Kalogerou, George Christopoulos & Marina Kleanthous. (2008) Hb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – –MED I Results in a Severe Form of Hb H Disease. Hemoglobin 32:3, pages 237-246.
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Ishwar C. Verma, Marina Kleanthous, Renu Saxena, Suthat Fucharoen, Pranee Winichagoon, Sheikh Raizuddin, Shaheen N. Khan, Mohammad T. Akbari, Mina Izadyar, Navratnam Kotea, John M. Old, Panayiotis A. Ioannou & Baldip Khan. (2007) Multicenter Study of the Molecular Basis of Thalassemia Intermedia in Different Ethnic Populations. Hemoglobin 31:4, pages 439-452.
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Ladan H. Gohari, Miranda Petrou, Xenia Felekis, George Christopoulos & Marina Kleanthous. (2003) Identification of α‐Thalassemia Mutations in Iranian Individuals with Abnormal Hematological Indices and Normal Hb A2. Hemoglobin 27:2, pages 129-132.
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Amine Zorai, Cornelis L. Harteveld, Achech Bakir, Peter Van Delft, Abdelaziz Falfoul, Koussay Dellagi, Salem Abbes & Piero C. Giordano. (2002) MOLECULAR SPECTRUM OF α-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH. Hemoglobin 26:4, pages 353-362.
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Articles from other publishers (19)

Bin Hashim Halim-Fikri, Carsten W. Lederer, Atif Amin Baig, Siti Nor Assyuhada Mat-Ghani, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wardah Yusof, Diana Abdul Rashid, Nurul Fatihah Azman, Suthat Fucharoen, Ramdan Panigoro, Catherine Lynn T. Silao, Vip Viprakasit, Norunaluwar Jalil, Norafiza Mohd Yasin, Rosnah Bahar, Veena Selvaratnam, Norsarwany Mohamad, Nik Norliza Nik Hassan, Ezalia Esa, Amanda Krause, Helen Robinson, Julia Hasler, Coralea Stephanou, Raja-Zahratul-Azma Raja-Sabudin, Jacques Elion, Ghada El-Kamah, Domenico Coviello, Narazah Yusoff, Zarina Abdul Latiff, Chris Arnold, John Burn, Petros Kountouris, Marina Kleanthous, Raj Ramesar & Bin Alwi Zilfalil. (2022) Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries. Journal of Personalized Medicine 12:4, pages 552.
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Petros Kountouris, Kyriaki Michailidou, Soteroula Christou, Michael Hadjigavriel, Maria Sitarou, Anita Kolnagou, Marina Kleanthous & Paul Telfer. (2020) Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus. Haematologica 106:9, pages 2458-2468.
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Achraf Laghmich, Fatima Zahra Alaoui Ismaili, Amina Barakat, Naima Ghailani Nourouti, Mohamed Khattab & Mohcine Bennani Mechita. (2019) Alpha-Thalassemia in North Morocco: Prevalence and Molecular Spectrum. BioMed Research International 2019, pages 1-7.
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Dipti Upadhye, Dipty Jain, Anita Nadkarni, Kanjaksha Ghosh & Roshan Colah. (2018) Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India. Indian Journal of Hematology and Blood Transfusion 35:1, pages 109-113.
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Petros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, George Christopoulos, Eleni Pavlou, Miranda Petrou, Xenia Feleki, Eleni Karitzie, Marios Phylactides, Pavlos Fanis, Carsten W. Lederer, Andreani R. Kyrri, Eleni Kalogerou, Christiana Makariou, Christiana Ioannou, Loukas Kythreotis, Georgia Hadjilambi, Nicoletta Andreou, Evangelia Pangalou, Irene Savvidou, Michael Angastiniotis, Michael Hadjigavriel, Maria Sitarou, Annita Kolnagou, Marina Kleanthous & Soteroula Christou. (2016) The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study. Scientific Reports 6:1.
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M.‐Y. Wu, X.‐M. Xie, J. Li & D.‐Z. Li. (2015) Neonatal screening for α‐thalassemia by cord hemoglobin Barts: how effective is it?. International Journal of Laboratory Hematology 37:5, pages 649-653.
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Muhammet Murat Celik, Ramazan Gunesacar, Gonul Oktay, Gulay Gulbol Duran & Hasan Kaya. (2013) Spectrum of α-thalassemia mutations including first observation of - -FIL deletion in Hatay Province, Turkey. Blood Cells, Molecules, and Diseases 51:1, pages 27-30.
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Pimlak Charoenkwan, Rawee Taweephol, Supatra Sirichotiyakul, Watcharee Tantiprabha, Rattika Sae-Tung, Sudjai Suanta, Pimonrat Sakdasirisathaporn & Torpong Sanguansermsri. (2010) Cord blood screening for α-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: Correlation with genotypes and hematologic parameters. Blood Cells, Molecules, and Diseases 45:1, pages 53-57.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 266 295 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
Al-Hilali AkramAbu Saud Khalida, Sofi Sawsan & La Cock Charles. (2009) Birth MCV and MCH are Quite Reliable Parameters for the Prediction of Alpha Thalassemia Trait. Clinical medicine. Blood disorders 2, pages CMBD.S1927.
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H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
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Jaruwan Tritipsombut, Kanokwan Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen, Nirut Siriratmanawong, Charnchai Pinmuang-ngam & Pattara Sanchaisuriya. (2008) Hemoglobin Profiles and Hematologic Features of Thalassemic Newborns: Application to Screening of α-Thalassemia 1 and Hemoglobin E. Archives of Pathology & Laboratory Medicine 132:11, pages 1739-1745.
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Orapan Sripichai, Thongperm Munkongdee, Chutima Kumkhaek, Saovaros Svasti, Pranee Winichagoon & Suthat Fucharoen. (2007) Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease. Annals of Hematology 87:5, pages 375-379.
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Nicos Skordis, Monica Michaelidou, Savvas C. Savva, Yiannis Ioannou, Andreas Rousounides, Marina Kleanthous, George Skordos & Soteroulla Christou. (2006) The impact of genotype on endocrine complications in thalassaemia major. European Journal of Haematology 77:2, pages 150-156.
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María Paulina Nava, Bertha Ibarra, María Teresa Magaña, María de la Luz Chávez & F. Javier Perea. (2006) Prevalence of −α3.7 and αααanti3.7 alleles in sickle cell trait and β-thalassemia patients in Mexico. Blood Cells, Molecules, and Diseases 36:2, pages 255-258.
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Anthi Drousiotou, Elias H Touma, Nicoletta Andreou, Jacques Loiselet, Michalis Angastiniotis, Brian C Verrelli & Sarah A Tishkoff. (2004) Molecular characterization of G6PD deficiency in Cyprus. Blood Cells, Molecules, and Diseases 33:1, pages 25-30.
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C.L. Harteveld, M. Yavarian, A. Zorai, E.D. Quakkelaar, P. van Delft & P.C. Giordano. (2003) Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects. American Journal of Hematology 74:2, pages 99-103.
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M. Kleanthous, K. Kyriacou, A. Kyrri, E. Kalogerou, PH. Vassiliades, A. Drousiotou, I. Kallikas, P. Ioannou & M. Angastiniotis. (2001) Alpha-thalassaemia prenatal diagnosis by two PCR-based methods. Prenatal Diagnosis 21:5, pages 413-417.
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