Hemoglobin, Volume 41, Issue 2 (2017)

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Hemoglobin, Volume 41, Issue 2 (2017)

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Original Article

Article
Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman
Sitthichai Panyasai & Sakorn Pornprasert
Pages: 73-76
Published online: 23 Jun 2017
AbstractforHematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman | Full Text | References | PDF (635.2 KB)
  • 74 Views
  • 1 CrossRef citations
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Article
Preliminary Evaluation of a Point-of-Care Testing Device (SickleSCAN™) in Screening for Sickle Cell Disease
Maxwell M. Nwegbu, Hezekiah A. Isa, Biyaya B. Nwankwo, Chinedu C. Okeke, Uduak J. Edet-Offong, Norah O. Akinola, Adekunle D. Adekile, John C. Aneke, Emmanuel C. Okocha, Thomas Ulasi, Usman Abjah, Ngozi I. Ugwu, Angela A. Okolo, Anazoeze Madu, Ifeoma Emodi, Ahmed Girei, Taiwo M. Balogun, Ijeoma N. Diaku-Akinwumi, Chinatu Ohiaeri, Biobele J. Brown, John A. Olaniyi, Abdulaziz Hassan, Sani Awwalu, Dorothy A. Okoh & Obiageli E. Nnodu
Pages: 77-82
Published online: 15 Jun 2017
AbstractforPreliminary Evaluation of a Point-of-Care Testing Device (SickleSCAN™) in Screening for Sickle Cell Disease | Full Text | References | PDF (996.2 KB)
  • 511 Views
  • 12 CrossRef citations
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Article
Hemoglobin Variant Profiles among Brazilian Quilombola Communities
Rayra P. Santiago, Rodrigo M. Oliveira, Leonardo F. Soares, Camylla V. B. Figueiredo, Denise Oliveira Silva, Ana F. Hurtado-Guerrero, Luciana M. Fiuza, Caroline C. Guarda, Elisângela V. Adorno, Cynara G. Barbosa & Marilda S. Gonçalves
Pages: 83-88
Published online: 07 Jun 2017
AbstractforHemoglobin Variant Profiles among Brazilian Quilombola Communities | Full Text | References | PDF (704.5 KB) | Supplemental
  • 109 Views
  • 5 CrossRef citations
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Article
Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2]
Fatou Gueye Tall, Cyril Martin, El Hadji Malick Ndour, Indou Déme Ly, Céline Renoux, Louis Chillotti, Nicolas Veyrenche, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Philippe Lacan, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall & Philippe Joly
Pages: 89-95
Published online: 03 Jul 2017
AbstractforGenetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2] | Full Text | References | PDF (1.4 MB)
  • 234 Views
  • 11 CrossRef citations
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Review Article
Molecular Characterization of β-Thalassemia Mutations in Central Vietnam
Maria G. Doro, Giuseppina Casu, Laura Frogheri, Ivana Persico, Le Phan Minh Triet, Phan Thi Thuy Hoa, Nguyen Huy Hoang, Monica Pirastru, Paolo Mereu, Francesco Cucca & Bruno Masala
Pages: 96-99
Published online: 03 Jul 2017
AbstractforMolecular Characterization of β-Thalassemia Mutations in Central Vietnam | Full Text | References | PDF (400 KB)
  • 190 Views
  • 6 CrossRef citations
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Article
Rare β-Globin Gene Mutations in Pakistan
Ahsan Hussain, Suhaib Ahmed, Nadir Ali, Hamid S. Mailk, Mariam Anees, Altaf H. Chuahdry & Parvez Ahmed
Pages: 100-103
Published online: 03 Jul 2017
AbstractforRare β-Globin Gene Mutations in Pakistan | Full Text | References | PDF (457.3 KB)
  • 242 Views
  • 3 CrossRef citations
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Article
Population-Based Genetic Study of β-Thalassemia Mutations in Mardan Division, Khyber Pakhtunkhwa Province, Pakistan
Raj Muhammad, Muhammad Shakeel, Shoaib U. Rehman & Muhammad A. Lodhi
Pages: 104-109
Published online: 21 Jun 2017
AbstractforPopulation-Based Genetic Study of β-Thalassemia Mutations in Mardan Division, Khyber Pakhtunkhwa Province, Pakistan | Full Text | References | PDF (680.5 KB)
  • 177 Views
  • 8 CrossRef citations
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Article
Comparison of MicroRNAs Mediated in Reactivation of the γ-Globin in β-Thalassemia Patients, Responders and Non-Responders to Hydroxyurea
Mohammad T. Hojjati, Azita Azarkeivan, Ali A. Pourfathollah & Naser Amirizadeh
Pages: 110-115
Published online: 11 Jul 2017
AbstractforComparison of MicroRNAs Mediated in Reactivation of the γ-Globin in β-Thalassemia Patients, Responders and Non-Responders to Hydroxyurea | Full Text | References | PDF (828.1 KB)
  • 204 Views
  • 7 CrossRef citations
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Article
Evaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate β-Thalassemia Trait from Iron Deficiency Anemia in the Thai Population
Sakorn Pornprasert, Choosak Thongsat & Uraiporn Panyachadporn
Pages: 116-119
Published online: 09 Jun 2017
AbstractforEvaluation of Applying a Combination of Red Cell Indexes and Formulas to Differentiate β-Thalassemia Trait from Iron Deficiency Anemia in the Thai Population | Full Text | References | PDF (400.6 KB)
  • 148 Views
  • 7 CrossRef citations
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Article
The Assessment of Skin Color and Iron Levels in Pediatric Patients with β-Thalassemia Major Using a Visual Skin Color Chart
Ibrahim H. Bucak, Habip Almis, Samet Benli & Mehmet Turgut
Pages: 120-123
Published online: 15 Jun 2017
AbstractforThe Assessment of Skin Color and Iron Levels in Pediatric Patients with β-Thalassemia Major Using a Visual Skin Color Chart | Full Text | References | PDF (638.1 KB)
  • 135 Views
  • 4 CrossRef citations
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Article
Design, Validation, and Clinical Implementation of a Gap-Polymerase Chain Reaction Method for α-Thalassemia Genotyping Using Capillary Electrophoresis
Basma Basha, Frank Mularo & James R. Cook
Pages: 124-130
Published online: 09 Jun 2017
AbstractforDesign, Validation, and Clinical Implementation of a Gap-Polymerase Chain Reaction Method for α-Thalassemia Genotyping Using Capillary Electrophoresis | Full Text | References | PDF (1.4 MB)
  • 397 Views
  • 8 CrossRef citations
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Short Communication

Rapid Communication
Decompensated Cirrhosis and Sickle Cell Disease: Case Reports and Review of the Literature
Roberta D’Ambrosio, Marco Maggioni, Maria F. Donato, Pietro Lampertico, Maria D. Cappellini & Giovanna Graziadei
Pages: 131-133
Published online: 11 Jul 2017
AbstractforDecompensated Cirrhosis and Sickle Cell Disease: Case Reports and Review of the Literature | Full Text | References | PDF (1,007.1 KB)
  • 206 Views
  • 4 CrossRef citations
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Rapid Communication
Hb Southampton [β106(G8)Leu→Pro; HBB: c.320T>C] and Codons 41/42 (–TTCT; HBB: c.124_127delTTCT) in a Chinese Girl
Jiaodi Liu, Yumei Huang, Yu Lei & Yongrong Lai
Pages: 134-136
Published online: 05 Jun 2017
AbstractforHb Southampton [β106(G8)Leu→Pro; HBB: c.320T>C] and Codons 41/42 (–TTCT; HBB: c.124_127delTTCT) in a Chinese Girl | Full Text | References | PDF (774.1 KB)
  • 73 Views
  • 5 CrossRef citations
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Rapid Communication
Detection of Hb Rothschild HBB: c.[112T>A or 112T>C], Through High Index of Suspicion on Abnormal Pulse Oximetry
Nazeer A. Alli, Piet Wessels, Narisha Rampersad, Barnaby E. Clark & Swee Lay Thein
Pages: 137-139
Published online: 16 Jun 2017
AbstractforDetection of Hb Rothschild HBB: c.[112T>A or 112T>C], Through High Index of Suspicion on Abnormal Pulse Oximetry | Full Text | References | PDF (485.1 KB)
  • 271 Views
  • 4 CrossRef citations
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Rapid Communication
Hb Amsterdam-A1 [α32(B13)Met→Ile; HBA1: c.99G>A]: A Hyperunstable Variant Due to a New Mutation on the α1 Gene
Stephen O. Brennan, Darrell Wang, Mark Horridge & Campbell R. Sheen
Pages: 140-143
Published online: 11 Jul 2017
AbstractforHb Amsterdam-A1 [α32(B13)Met→Ile; HBA1: c.99G>A]: A Hyperunstable Variant Due to a New Mutation on the α1 Gene | Full Text | References | PDF (828.8 KB)
  • 112 Views
  • 7 CrossRef citations
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Rapid Communication
New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F
Hussam Ghoti, Eitan Fibach, Eliezer A. Rachmilewitz, Hisham Jeadi & Dvora Filon
Pages: 144-146
Published online: 03 Jul 2017
AbstractforNew Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F | Full Text | References | PDF (544 KB)
  • 119 Views
  • 5 CrossRef citations
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Rapid Communication
Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome
Faten Haddad, Nawel Trabelsi, Leila Chaouch, Imen Darragi, Meriem Oueslati, Imen Boudriga, Dorra Chaouachi, Wijdene El-Borgi, Raouf Hafsia, Salem Abbes & Houyem Ouragini
Pages: 147-150
Published online: 08 Jun 2017
AbstractforHomozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome | Full Text | References | PDF (729.4 KB)
  • 154 Views
  • 4 CrossRef citations
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