Hemoglobin, Volume 38, Issue 5 (2014)

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Hemoglobin, Volume 38, Issue 5 (2014)

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Mini Reviews

Review Article
Thalassemias and Hemoglobinopathies in Turkey
Duran Canatan
Pages: 305-307
Published online: 17 Jul 2014
AbstractforThalassemias and Hemoglobinopathies in Turkey | Full Text | References | PDF (245.6 KB)
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Review Article

Review Article
Preventing Thalassemia in Lebanon: Successes and Challenges in a Developing Country
Michele Abi Saad, Anthony G. Haddad, Elie S. Alam, Sanaa Aoun, Pascale Maatouk, Najat Ajami, Therese Khairallah, Suzanne Koussa, Khaled M. Musallam & Ali T. Taher
Pages: 308-311
Published online: 17 Jul 2014
AbstractforPreventing Thalassemia in Lebanon: Successes and Challenges in a Developing Country | Full Text | References | PDF (389.8 KB)
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Original Article

Article
Adult Sickle Cell Disease Epidemiology and the Potential Role of a Multidisciplinary Comprehensive Care Center in a City with Low Prevalence
Andrew Binding, Karen Valentine, Man-Chiu Poon & Farzana A. Sayani
Pages: 312-315
Published online: 15 Sep 2014
AbstractforAdult Sickle Cell Disease Epidemiology and the Potential Role of a Multidisciplinary Comprehensive Care Center in a City with Low Prevalence | Full Text | References | PDF (121.5 KB)
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Research Article

Article
Blood Typing Profile of a School-Aged Population of a North Togo Township
Ahoefa Vovor, Lochina Fétéké, Irénée M. Kueviakoe, Laye Kpatarou, Koffi Mawussi, Hézouwè Magnang & Akuété Y. Ségbéna
Pages: 316-318
Published online: 01 Oct 2014
AbstractforBlood Typing Profile of a School-Aged Population of a North Togo Township | Full Text | References | PDF (112.7 KB)
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Article
Characterization of Two Unique α-Globin Gene Cluster Deletions Causing α-Thalassemia in Israeli Arabs
Oded Gilad, Orly Dgany, Sharon Noy-Lotan, Tania Krasnov, Sarah Elitzur, Serge Pissard, Iris Kventsel, Joanne Yacobovich & Hannah Tamary
Pages: 319-324
Published online: 15 Sep 2014
AbstractforCharacterization of Two Unique α-Globin Gene Cluster Deletions Causing α-Thalassemia in Israeli Arabs | Full Text | References | PDF (461.8 KB)
  • 172 Views
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Article
The Spectrum of β-Thalassemia Mutations in Hatay, Turkey: Reporting Three New Mutations
Ozgur Aldemir, Muzeyyen Izmirli & Hasan Kaya
Pages: 325-328
Published online: 26 Aug 2014
AbstractforThe Spectrum of β-Thalassemia Mutations in Hatay, Turkey: Reporting Three New Mutations | Full Text | References | PDF (125 KB)
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Article
β-Thalassemia Mutations in Western India: Outcome of Prenatal Diagnosis in a Hemoglobinopathies Project
Ashwin P. Patel, Rupesh B. Patel, Saumyaa A. Patel, Salil N. Vaniawala, Dipika S. Patel, Naina S. Shrivastava, Narmadeshwar P. Sharma, Jayendrasinh V. Zala, Prakash H. Parmar & Madhuben R. Naik
Pages: 329-334
Published online: 15 Sep 2014
Abstractforβ-Thalassemia Mutations in Western India: Outcome of Prenatal Diagnosis in a Hemoglobinopathies Project | Full Text | References | PDF (489.6 KB)
  • 200 Views
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Article
The Correlation of α-Globin Gene Mutations and the XmnI Polymorphism with Clinical Severity of Hb E/β-Thalassemia
Pimlak Charoenkwan, Pimjan Teerachaimahit & Torpong Sanguansermsri
Pages: 335-338
Published online: 19 Sep 2014
AbstractforThe Correlation of α-Globin Gene Mutations and the XmnI Polymorphism with Clinical Severity of Hb E/β-Thalassemia | Full Text | References | PDF (122.4 KB)
  • 207 Views
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Article
Expression of CD55 on Red Blood Cells of β-Thalassemia Patients
Jamil M.A.S. Obaid, Salma Y. Abo El-Nazar, Amal M. Ghanem, Abeer S. El-Hadidi & Basma H.M. Mersal
Pages: 339-344
Published online: 15 Jul 2014
AbstractforExpression of CD55 on Red Blood Cells of β-Thalassemia Patients | Full Text | References | PDF (962.9 KB)
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Article
Incidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents
Archwin Tanphaichitr, Thisarat Kusuwan, Siriporn Limviriyakul, Suvajana Atipas, Julaporn Pooliam, Tuangrat Sangpraypan, Voravarn S. Tanphaichitr & Vip Viprakasit
Pages: 345-350
Published online: 22 Jul 2014
AbstractforIncidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents | Full Text | References | PDF (225.7 KB)
  • 287 Views
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Article
Priapism, an Emerging Complication in β-Thalassemia Intermedia Patients
Naji S. Mallat, David Wehbe, Anthony Haddad, Maria D. Cappellini, Alessia Marcon, Suzanne Koussa, Miguel R. Abboud, Amr Radwan & Ali T. Taher
Pages: 351-354
Published online: 01 Oct 2014
AbstractforPriapism, an Emerging Complication in β-Thalassemia Intermedia Patients | Full Text | References | PDF (344.6 KB)
  • 168 Views
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Article
A Local Equation for Differential Diagnosis of β-Thalassemia Trait and Iron Deficiency Anemia by Logistic Regression Analysis in Southeast Iran
Narjes Sargolzaie & Ebrahim Miri-Moghaddam
Pages: 355-358
Published online: 26 Aug 2014
AbstractforA Local Equation for Differential Diagnosis of β-Thalassemia Trait and Iron Deficiency Anemia by Logistic Regression Analysis in Southeast Iran | Full Text | References | PDF (169.2 KB)
  • 165 Views
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Article
N-Acetylcysteine Supplementation Reduces Oxidative Stress and DNA Damage in Children with β-Thalassemia
Zeynep Canan Ozdemir, Ahmet Koc, Ali Aycicek & Abdurrahim Kocyigit
Pages: 359-364
Published online: 15 Sep 2014
AbstractforN-Acetylcysteine Supplementation Reduces Oxidative Stress and DNA Damage in Children with β-Thalassemia | Full Text | References | PDF (315.6 KB)
  • 313 Views
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Article
Correlation of Iron Overload and Glomerular Filtration Rate Estimated by Cystatin C in Patients with β-Thalassemia Major
Murtadha Al-Khabori, Sunil Bhandari, Khalid Al-Rasadi, Surekha Mevada, Hamoud Al-Dhuhli, Nasser Al-Kemyani & Shahina Daar
Pages: 365-368
Published online: 30 Jul 2014
AbstractforCorrelation of Iron Overload and Glomerular Filtration Rate Estimated by Cystatin C in Patients with β-Thalassemia Major | Full Text | References | PDF (356.7 KB)
  • 199 Views
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Article
Characterization of Hb Calvino (HBB: c.406G > A): A New Silent β-Globin Gene Variant Found in Coexistence with α-Thalassemia in a Family of African Origin
Maria Marsella, Gianluca Salvagno, Bernadetta Dolcini, Alessandra Ferlini, Anna Ravani, Cornelis L. Harteveld, Piero C. Giordano & Caterina Borgna-Pignatti
Pages: 369-372
Published online: 15 Sep 2014
AbstractforCharacterization of Hb Calvino (HBB: c.406G > A): A New Silent β-Globin Gene Variant Found in Coexistence with α-Thalassemia in a Family of African Origin | Full Text | References | PDF (386.1 KB)
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Short Communications

Article
Primary Stroke in a Woman With Sickle Cell Anemia Responsive to Hydroxyurea Therapy
Samir K. Ballas, Ubaldo Martinez & Michael Savage
Pages: 373-375
Published online: 19 Sep 2014
AbstractforPrimary Stroke in a Woman With Sickle Cell Anemia Responsive to Hydroxyurea Therapy | Full Text | References | PDF (100.4 KB)
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Research Article

Article
Two New γ Chain Variants: Hb F-Augusta GA [Gγ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [Aγ125(H3)Glu → Ala; HBG1: c.377A > C]
Ferdane Kutlar, Afshin Ameri, Niren H. Patel, Lina Zhuang, Lee E. Johnson, Michael L. Cheng & Abdullah Kutlar
Pages: 376-380
Published online: 01 Oct 2014
AbstractforTwo New γ Chain Variants: Hb F-Augusta GA [Gγ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [Aγ125(H3)Glu → Ala; HBG1: c.377A > C] | Full Text | References | PDF (1.5 MB)
  • 83 Views
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