Hemoglobin, Volume 41, Issue 1 (2017)

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Hemoglobin, Volume 41, Issue 1 (2017)

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Original Article

Article
Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity
Saskia Brunner-Agten, Thomas von Känel, Benno Röthlisberger, Charles Broquet & Andreas R. Huber
Pages: 1-5
Published online: 22 May 2017
AbstractforHb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity | Full Text | References | PDF (1,023.4 KB)
  • 157 Views
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Article
Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease
Maria P. Yavropoulou, Maria Pikilidou, Despoina Pantelidou, Dimitrios G. Tsalikakis, Athanasios Mousiolis, Panagiota Chalkia, John G. Yovos & Pantelis Zebekakis
Pages: 6-11
Published online: 03 Apr 2017
AbstractforInsulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease | Full Text | References | PDF (894.6 KB)
  • 185 Views
  • 6 CrossRef citations
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Article
Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil
Gisele C.S. Carrocini, Larissa P.R. Venancio, Viviani L.R. Pessoa, Clarisse L.C. Lobo & Claudia R. Bonini-Domingos
Pages: 12-15
Published online: 03 Apr 2017
AbstractforMutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil | Full Text | References | PDF (483.8 KB)
  • 271 Views
  • 2 CrossRef citations
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Article
Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt
Soheir Adam, Hanan Afifi, Manal Thomas, Phoebe Magdy & Ghada El-Kamah
Pages: 16-20
Published online: 25 Apr 2017
AbstractforQuality of Life Outcomes in a Pediatric Thalassemia Population in Egypt | Full Text | References | PDF (472.4 KB)
  • 274 Views
  • 14 CrossRef citations
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Article
Utility of Transient Elastography in Estimating Hepatic Iron Concentration in Comparison to Magnetic Resonance Imaging in Patients Who are Transfusion-Dependent: A Canadian Center Experience
George Ou, Hin Hin Ko, Pari Tiwari, Navdeep Sandhu, Cherry Galorport, Terry Lee & Hatoon Ezzat
Pages: 21-25
Published online: 22 May 2017
AbstractforUtility of Transient Elastography in Estimating Hepatic Iron Concentration in Comparison to Magnetic Resonance Imaging in Patients Who are Transfusion-Dependent: A Canadian Center Experience | Full Text | References | PDF (705.8 KB)
  • 101 Views
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Article
Prevalence of Anemia and Hemoglobin Disorders Among School Children in Myanmar
Saw Thu Wah, Yoon Shwe Yi, Aye Aye Khin, Chotiros Plabplueng & Pornlada Nuchnoi
Pages: 26-31
Published online: 02 Apr 2017
AbstractforPrevalence of Anemia and Hemoglobin Disorders Among School Children in Myanmar | Full Text | References | PDF (773.5 KB)
  • 360 Views
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Article
A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran
Hajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, Mohsen Vakili, Sadegh Sedaghat, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki
Pages: 32-37
Published online: 07 Apr 2017
AbstractforA Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran | Full Text | References | PDF (801.2 KB)
  • 147 Views
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Article
The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
Prapapun Leckngam, Ektong Limweeraprajak, Tiemjan Kiewkarnkha & Thanusak Tatu
Pages: 38-43
Published online: 16 Apr 2017
AbstractforThe Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels | Full Text | References | PDF (697 KB)
  • 272 Views
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Article
IVS-II-648/649 (–T) (HBB: c.316−202del) Triggers a Novel β-Thalassemia Phenotype
Azam Azimi, Reza Alibakhshi, Hasibeh Hayati, Soosan Tahmasebi & Sasan Alimoradi
Pages: 44-46
Published online: 05 May 2017
AbstractforIVS-II-648/649 (–T) (HBB: c.316−202del) Triggers a Novel β-Thalassemia Phenotype | Full Text | References | PDF (575.1 KB)
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Short Communication

Rapid Communication
Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia
Yan Li, Jin-Mei Yan, Jian-Ying Zhou, Yue-Cheng Lu & Dong-Zhi Li
Pages: 47-49
Published online: 03 Apr 2017
AbstractforCombination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia | Full Text | References | PDF (655.8 KB)
  • 73 Views
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Rapid Communication
Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family
Allan Pernudy-Ubau, Jaslyn Salinas-Molina, Yaneris Requenez, Marianela Ortiz-Lopez, Ann-Christin Puller, Kenia García-Rosales, Anaishelle Rodríguez-Estrada, Walter Rodríguez-Romero, Gerardo Mejía-Baltodano, Hong-Yuan Luo & David H.K. Chui
Pages: 50-52
Published online: 11 Apr 2017
AbstractforHb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family | Full Text | References | PDF (605.6 KB)
  • 138 Views
  • 1 CrossRef citations
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Rapid Communication
A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant
Maria Pia Cappabianca, Alessia Colosimo, Annalaura Sabatucci, Enrico Dainese, Paola Di Biagio, Roberta Piscitelli, Ofelia Sarra, Daniela Zei & Antonio Amato
Pages: 53-55
Published online: 10 Apr 2017
AbstractforA Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant | Full Text | References | PDF (685.5 KB)
  • 114 Views
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Rapid Communication
A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA)
Biyan Chen, Li Lin, Shang Yi, Qiuli Chen, Hongwei Wei, Guojian Li, Chenguang Zheng, Sheng He & XiaoXia Qiu
Pages: 56-58
Published online: 11 Apr 2017
AbstractforA Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA) | Full Text | References | PDF (500.7 KB)
  • 88 Views
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Rapid Communication
A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia
Fan Jiang, Lv-Yin Huang, Gui-Lan Chen, Jian-Ying Zhou, Xing-Mei Xie & Dong-Zhi Li
Pages: 59-60
Published online: 01 May 2017
AbstractforA Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia | Full Text | References | PDF (402.4 KB)
  • 104 Views
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Rapid Communication
The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran
Masoumeh Jalilian, Farid Azizi Jalilian, Leila Ahmadi, Razieh Amini, Hossein Esfehani, Maryam Sosanian, Bahareh Rabbani, Majid Maleki & Nejat Mahdieh
Pages: 61-64
Published online: 10 Apr 2017
AbstractforThe Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran | Full Text | References | PDF (588 KB)
  • 307 Views
  • 8 CrossRef citations
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Rapid Communication
A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T]
Li Lin, Biyan Chen, Shang Yi, Qiuli Chen, Hongwei Wei, Guojian Li, Chenguang Zheng, Xiao-Xia Qiu & Sheng He
Pages: 65-67
Published online: 02 Apr 2017
AbstractforA Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T] | Full Text | References | PDF (578.5 KB)
  • 94 Views
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Rapid Communication
Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family
Sheng He, Qian Qin, Li Lin, Qiuli Chen, Shang Yi, Honhwei Wei, Juan Du, Chenguang Zheng, Xiaoxia Qiu & Biyan Chen
Pages: 68-72
Published online: 05 May 2017
AbstractforComplex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family | Full Text | References | PDF (1.4 MB)
  • 140 Views
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