Hemoglobin, Volume 38, Issue 3 (2014)

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Hemoglobin, Volume 38, Issue 3 (2014)

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Original Article

Article
Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience
Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi
Pages: 153-157
Published online: 14 May 2014
AbstractforCharacterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience | Full Text | References | PDF (135.6 KB)
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Research Article

Article
Screening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a Prenatal Control Program for Thalassemia
Yu Yang, Ji-Wu Lou, Yan-Hui Liu, Yi He & Dong-Zhi Li
Pages: 158-160
Published online: 14 May 2014
AbstractforScreening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a Prenatal Control Program for Thalassemia | Full Text | References | PDF (115 KB)
  • 271 Views
  • 13 CrossRef citations
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Article
α-Globin Gene Mutations in Isfahan Province, Iran
Arezo Karamzade, Hadi Mirzapour, Majid Hoseinzade, Sara Asadi, Tahere Gholamrezapour, Parvaneh Tavakoli & Mansoor Selebi
Pages: 161-164
Published online: 14 May 2014
Abstractforα-Globin Gene Mutations in Isfahan Province, Iran | Full Text | References | PDF (294.4 KB)
  • 137 Views
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Article
α-Thalassemia Does Not Seem to Influence Erythrocyte Deformability in Sickle Cell Trait Carriers
Amparo Vayá, Susana Collado, Rafael Alis, Belen Vera, Marco Romagnoli & Eva Barragán
Pages: 165-168
Published online: 07 Mar 2014
Abstractforα-Thalassemia Does Not Seem to Influence Erythrocyte Deformability in Sickle Cell Trait Carriers | Full Text | References | PDF (120 KB)
  • 132 Views
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Article
Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50)
Chris Adhiyanto, Yukio Hattori, Yasuhiro Yamashiro, Ferania Mella, Takenori Nitta, Mizuki Iihoshi, Satsuki Araki, Maryam Matar & Fumiya Takagi
Pages: 169-172
Published online: 10 Mar 2014
AbstractforOxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50) | Full Text | References | PDF (124 KB)
  • 83 Views
  • 7 CrossRef citations
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Article
Prevalence of Low Bone Mass and Vitamin D Deficiency in β-Thalassemia Major
Ploutarchos Tzoulis, Ai Leen Ang, Farrukh T. Shah, Marko Berovic, Emma Prescott, Romilla Jones & Maria Barnard
Pages: 173-178
Published online: 24 Apr 2014
AbstractforPrevalence of Low Bone Mass and Vitamin D Deficiency in β-Thalassemia Major | Full Text | References | PDF (142.5 KB)
  • 232 Views
  • 21 CrossRef citations
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Article
Evaluation of the National Prevention Program in Iran, 2007–2009: the Accomplishments and Challenges with Reflections on the Path Ahead
Mahmoud Hadipour Dehshal, Mehdi Tabrizi Namini, Alireza Ahmadvand, Mohsen Manshadi, Forouzan Sadeghian Varnosfaderani & Hassan Abolghasemi
Pages: 179-187
Published online: 26 Mar 2014
AbstractforEvaluation of the National Prevention Program in Iran, 2007–2009: the Accomplishments and Challenges with Reflections on the Path Ahead | Full Text | References | PDF (471.6 KB)
  • 120 Views
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Article
Proteasome Inhibition Induces Both Antioxidant and Hb F Responses in Sickle Cell Disease Via the Nrf2 Pathway
Vinod Pullarkat, Zhuo Meng, Stanley M. Tahara, Cage S. Johnson & Vijay K. Kalra
Pages: 188-195
Published online: 26 Mar 2014
AbstractforProteasome Inhibition Induces Both Antioxidant and Hb F Responses in Sickle Cell Disease Via the Nrf2 Pathway | Full Text | References | PDF (738.7 KB)
  • 354 Views
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Article
Challenge of Managing Sickle Cell Disease in a Pediatric Population Living in Kinshasa, Democratic Republic of Congo: A Sickle Cell Center Experience
Michel Ntetani Aloni & Leonard Nkee
Pages: 196-200
Published online: 26 Mar 2014
AbstractforChallenge of Managing Sickle Cell Disease in a Pediatric Population Living in Kinshasa, Democratic Republic of Congo: A Sickle Cell Center Experience | Full Text | References | PDF (135.3 KB)
  • 331 Views
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Article
A Study of δ-Globin Gene Mutations in the UK Population: Identification of Three Novel Variants and Development of a Novel DNA Test for Hb A′2
Mohamed S. M. Khalil, Samy Marouf, David Element, Adele Timbs, Alice Gallienne, Anna Schuh, John M. Old & Shirley Henderson
Pages: 201-206
Published online: 06 Mar 2014
AbstractforA Study of δ-Globin Gene Mutations in the UK Population: Identification of Three Novel Variants and Development of a Novel DNA Test for Hb A′2 | Full Text | References | PDF (487.8 KB)
  • 279 Views
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Short Communications

Article
Two New Hemoglobin Variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb Madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]
Ferdane Kutlar, Yoram Unguru, Natalia Dixon, Niren Patel, Lakiea Bailey, Lina Zhuang, Harris Carmichael & Abdullah Kutlar
Pages: 207-210
Published online: 29 Jan 2014
AbstractforTwo New Hemoglobin Variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb Madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A] | Full Text | References | PDF (963.4 KB)
  • 75 Views
  • 1 CrossRef citations
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Research Article

Article
Hb Manukau [β67(E11)Val → Gly; HBB: c.203T>G]: The Role of Genetic Testing in the Diagnosis of Idiopathic Hemolytic Anemia
Mudra Kohli Kumar, Courtney Judd, James D. Hoyer, Kenneth C. Swanson, Linda Nelson & Jennifer L. Oliveira
Pages: 211-212
Published online: 10 Mar 2014
AbstractforHb Manukau [β67(E11)Val → Gly; HBB: c.203T>G]: The Role of Genetic Testing in the Diagnosis of Idiopathic Hemolytic Anemia | Full Text | References | PDF (101.2 KB)
  • 231 Views
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Article
Novel Point Mutation of the α2-Globin Gene (HBA2) and a Rare 2.4 kb Deletion of the α1-Globin Gene (HBA1), Identified in Two Chinese Patients with Hb H Disease
Chi-Chiu So, Amy Y. Y. Chan & Edmond S. K. Ma
Pages: 213-215
Published online: 14 May 2014
AbstractforNovel Point Mutation of the α2-Globin Gene (HBA2) and a Rare 2.4 kb Deletion of the α1-Globin Gene (HBA1), Identified in Two Chinese Patients with Hb H Disease | Full Text | References | PDF (883.2 KB)
  • 191 Views
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Article
Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates
Andrew Turner, Jurgen Sasse & Aniko Varadi
Pages: 216-220
Published online: 14 May 2014
AbstractforHb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates | Full Text | References | PDF (993.9 KB)
  • 182 Views
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Article
Low-Molecular-Weight Heparins for Managing Vasoocclusive Crises in People With Sickle Cell Disease: A Summary of a Cochrane Systematic Review
Esther J. van Zuuren & Zbys Fedorowicz
Pages: 221-223
Published online: 14 May 2014
AbstractforLow-Molecular-Weight Heparins for Managing Vasoocclusive Crises in People With Sickle Cell Disease: A Summary of a Cochrane Systematic Review | Full Text | References | PDF (315.6 KB)
  • 160 Views
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Erratum

Correction
Correction to: Incidence of the Hb E [β26(B8)Glu → Lys, GAG > AAG] Variant in Totos, one of the Smallest Primitive Tribes in the World
Page: 224
Published online: 14 May 2014
CitationforCorrection to: Incidence of the Hb E [β26(B8)Glu → Lys, GAG > AAG] Variant in Totos, one of the Smallest Primitive Tribes in the World | Full Text | PDF (76.4 KB)
  • 234 Views
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