Hemoglobin, Volume 37, Issue 2 (2013)

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Hemoglobin, Volume 37, Issue 2 (2013)

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Original Article

Article
Hb Treviso [α91(FG3)Leu→Phe (α2)]: A New Slightly Unstable Hemoglobin Variant with Moderately Decreased Oxygen Affinity
Giuseppina Barberio, Daniela Leone, Giovanni Ivaldi & Piero C. Giordano
Pages: 107-111
Published online: 25 Jan 2013
AbstractforHb Treviso [α91(FG3)Leu→Phe (α2)]: A New Slightly Unstable Hemoglobin Variant with Moderately Decreased Oxygen Affinity | Full Text | References | PDF (177.8 KB)
  • 107 Views
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Article
Association in Cis of the Mutations +20 (C>T) in the 5′ Untranslated Region and IVS-II-745 (C>G) on the β-Globin Gene
Paloma Ropero, Fernando A. González, Elena Cela, Cristina Beléndez, Aurea Cervera, Jorge Martínez-Nieto, Félix de la Fuente-Gonzalo, Lara Vinuesa, Ana Villegas & Joaquín Díaz-Mediavilla
Pages: 112-118
Published online: 21 Feb 2013
AbstractforAssociation in Cis of the Mutations +20 (C>T) in the 5′ Untranslated Region and IVS-II-745 (C>G) on the β-Globin Gene | Full Text | References | PDF (204.7 KB)
  • 319 Views
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Article
Misdiagnosis of Hb D-Punjab/β-Thalassemia is a Potential Pitfall in Hemoglobinopathy Screening Programs: A Case Report
Khawla M. Belhoul, Maisam L. Bakir & Mahera Abdulrahman
Pages: 119-123
Published online: 20 Feb 2013
AbstractforMisdiagnosis of Hb D-Punjab/β-Thalassemia is a Potential Pitfall in Hemoglobinopathy Screening Programs: A Case Report | Full Text | References | PDF (72.4 KB)
  • 254 Views
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Article
Secular Trends in the National and Provincial Births of New Thalassemia Cases in Iran From 2001 to 2006
Mahmoud Hadipour Dehshal, Alireza Ahmadvand, Sakineh Yousefi Darestani, Mohsen Manshadi & Hassan Abolghasemi
Pages: 124-137
Published online: 07 Mar 2013
AbstractforSecular Trends in the National and Provincial Births of New Thalassemia Cases in Iran From 2001 to 2006 | Full Text | References | PDF (308.5 KB) | Supplemental
  • 83 Views
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Article
Sistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran
Ebrahim Miri-Moghaddam, Azita Zadeh-Vakili, Abbas Nikravesh, Shohreh Sanei Sistani & Mehrnaz Naroie-Nejad
Pages: 138-147
Published online: 26 Feb 2013
AbstractforSistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran | Full Text | References | PDF (184.1 KB)
  • 97 Views
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Article
Novel Mutations Responsible for α-Thalassemia in Iranian Families
Nooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, Negin Faramarzi, Mehri Ashki, Shadi Vakili, Hashem Imanian, Mohsen Khosravi, Azita Azar-Keivan & Hossein Najmabadi
Pages: 148-159
Published online: 12 Feb 2013
AbstractforNovel Mutations Responsible for α-Thalassemia in Iranian Families | Full Text | References | PDF (171 KB)
  • 242 Views
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Article
Thalassemia and Premarital Screening: Potential for Implementation of a Screening Program Among Young People in Pakistan
Arslan Mirza, Alina Ghani, Anam Pal, Abeer Sami, Sana Hannan, Zohaib Ashraf, Sulala Iqbal, Umair Zafar Malik, Umar Hayat & Zafar Fatmi
Pages: 160-170
Published online: 07 Mar 2013
AbstractforThalassemia and Premarital Screening: Potential for Implementation of a Screening Program Among Young People in Pakistan | Full Text | References | PDF (232.9 KB)
  • 177 Views
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Short Communication

Article
Identification of the First Mutation in a Bre Motif of the β-Globin Gene and its Inheritance with two Other α-Globin Gene Mutations in a Lebanese Family
Adlette Inati, Hussein A Abbas, Jad Al-Danaf, Mirna Souaid, Mario Kahale, Suzan Koussa, Therese Abou Nasr, Lance Davis, Hong-Yuan Luo & David H.K. Chui
Pages: 171-175
Published online: 07 Mar 2013
AbstractforIdentification of the First Mutation in a Bre Motif of the β-Globin Gene and its Inheritance with two Other α-Globin Gene Mutations in a Lebanese Family | Full Text | References | PDF (184.2 KB)
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Article
Detection of Coinherited Hb H-Constant Spring/Paksé Disease and Hb E by Capillary Electrophoresis and High Performance Liquid Chromatography
Sakorn Pornprasert & Jarurin Waneesorn
Pages: 176-182
Published online: 13 Dec 2012
AbstractforDetection of Coinherited Hb H-Constant Spring/Paksé Disease and Hb E by Capillary Electrophoresis and High Performance Liquid Chromatography | Full Text | References | PDF (181.5 KB)
  • 219 Views
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Article
Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α+-Thalassemia in the Portuguese Population
Elizabete Cunha, Celeste Bento, Ana Oliveira, Luís Relvas, Joana Neves, Mariline Gameiro, Cristina Barros, Ana Araújo, Ana Macedo, Paula Rocha, Ricardo Costa, Tabita Maia & M. Letícia Ribeiro
Pages: 183-187
Published online: 31 Jan 2013
AbstractforHb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α+-Thalassemia in the Portuguese Population | Full Text | References | PDF (126.8 KB)
  • 96 Views
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Article
Codon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) Causing Nondeletional α-Thalassemia in a Chinese Family
Can Liao, Hai-Shen Tang, Ru Li & Dong-Zhi Li
Pages: 188-191
Published online: 07 Mar 2013
AbstractforCodon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) Causing Nondeletional α-Thalassemia in a Chinese Family | Full Text | References | PDF (316.4 KB)
  • 89 Views
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Article
Microdeletion Of Exon 3 In The HBA2 Gene Associated With Mild α-Thalassemia Trait
Anne Lambert, Ann Y.K. Wong, Yohji Kominami, Valerie C. Smith, Suseela Reddy, Louis D. Wadsworth, Nicholas H.C. Au & Ross T.A. MacGillivray
Pages: 192-196
Published online: 29 Jan 2013
AbstractforMicrodeletion Of Exon 3 In The HBA2 Gene Associated With Mild α-Thalassemia Trait | Full Text | References | PDF (227.8 KB)
  • 105 Views
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Article
Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in Heterozygotes Combined With β-Thalassemia
You-Qiong Li, Ru Li & Dong-Zhi Li
Pages: 197-200
Published online: 08 Feb 2013
AbstractforDetection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in Heterozygotes Combined With β-Thalassemia | Full Text | References | PDF (211.2 KB)
  • 135 Views
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Article
Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)
John S. Waye, Barry Eng, Laurie Hellens, Betty-Ann Hohenadel, Lisa M. Nakamura & Lynda Walker
Pages: 201-204
Published online: 11 Feb 2013
AbstractforNormal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C) | Full Text | References | PDF (233.5 KB)
  • 162 Views
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