Hemoglobin, Volume 38, Issue 2 (2014)

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Hemoglobin, Volume 38, Issue 2 (2014)

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Original Article

Article
Hb Ashburton [β12(A9)Thr → Pro; HBB: c.37A > C], a Novel, Mildly Unstable Variant and the First Substitution Identified at Codon 12
Stephen O. Brennan, Anthea Povall & Ulrich Lankes
Pages: 79-83
Published online: 29 Jan 2014
AbstractforHb Ashburton [β12(A9)Thr → Pro; HBB: c.37A > C], a Novel, Mildly Unstable Variant and the First Substitution Identified at Codon 12 | Full Text | References | PDF (575.8 KB)
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Research Article

Article
A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]
Elisabeth Saller, Elisabeth Kohne, Fabrizio Dutly & Hannes Frischknecht
Pages: 84-87
Published online: 07 Feb 2014
AbstractforA New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A] | Full Text | References | PDF (317.4 KB)
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Article
A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]
Imen Moumni, Amine Zorai, Sonia Mahjoub, Ikbel Mosbahi, Dorra Chaouechi, Neila Benromdhane & Salem Abbes
Pages: 88-90
Published online: 29 Jan 2014
AbstractforA New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A] | Full Text | References | PDF (356 KB)
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Article
Maternal and Perinatal Outcome of Women With Sickle Cell Disease of a Tribal Population in Central India
Neeta Natu, Seema Khandelwal, Ravindra Kumar & Anupama Dave
Pages: 91-94
Published online: 13 Jan 2014
AbstractforMaternal and Perinatal Outcome of Women With Sickle Cell Disease of a Tribal Population in Central India | Full Text | References | PDF (132.8 KB)
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Article
Leg Amputation for an Extensive, Severe and Intractable Sickle Cell Anemia Ulcer in a Brazilian Patient
Ana Maria Mach Queiroz, Jessica Campos, Clarisse Lobo, Claudia Regina Bonini-Domingos, Gilberto Cardoso & Samir K. Ballas
Pages: 95-98
Published online: 29 Jan 2014
AbstractforLeg Amputation for an Extensive, Severe and Intractable Sickle Cell Anemia Ulcer in a Brazilian Patient | Full Text | References | PDF (476.4 KB)
  • 86 Views
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Article
Patients Welcome the Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART)
Nirmish Shah, Jude Jonassaint & Laura De Castro
Pages: 99-103
Published online: 10 Feb 2014
AbstractforPatients Welcome the Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART) | Full Text | References | PDF (134.7 KB)
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Article
Joint Diabetes Thalassaemia Clinic: An Effective New Model of Care
Ploutarchos Tzoulis, Farrukh Shah, Romilla Jones, Emma Prescott & Maria Barnard
Pages: 104-110
Published online: 18 Dec 2013
AbstractforJoint Diabetes Thalassaemia Clinic: An Effective New Model of Care | Full Text | References | PDF (161.3 KB)
  • 109 Views
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Article
Combined Chelation Therapy with Deferoxamine and Deferiprone in β-Thalassemia Major: Compliance and Opinions of Young Thalassemic Patients
Emmanuel S. Hatzipantelis, Konstantinos Karasmanis, Vassilios Perifanis, Efthimia Vlachaki, Konstantinos Tziomalos & Marina Economou
Pages: 111-114
Published online: 18 Dec 2013
AbstractforCombined Chelation Therapy with Deferoxamine and Deferiprone in β-Thalassemia Major: Compliance and Opinions of Young Thalassemic Patients | Full Text | References | PDF (134.8 KB)
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Article
Report on Patients with Non Transfusion-Dependent β-Thalassemia Major Being Treated with Hydroxyurea Attending the Thalassemia Research Center, Sari, Mazandaran Province, Islamic Republic of Iran in 2013
Mehrnoush Kosaryan, Hossein Karami, Mandana Zafari & Negar Yaghobi
Pages: 115-118
Published online: 29 Jan 2014
AbstractforReport on Patients with Non Transfusion-Dependent β-Thalassemia Major Being Treated with Hydroxyurea Attending the Thalassemia Research Center, Sari, Mazandaran Province, Islamic Republic of Iran in 2013 | Full Text | References | PDF (188.5 KB)
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Article
Assessment of Iron Overload in Very Young Children with Limited Thalassemia Care Resources in South China
Wing-Yan Au, Chun Fu Li, Jian Pei Fang, Guang Fu Chen, Xin Sun, Chang Gang Li, Xin Hua Zhang, Xue Dong Wu, Hong Ying Gao, Wen Ge Hao, Darshana Rasalkar, Min Deng, Sio Peng A. Mok, Fernando Tricta & Winnie C.W. Chu
Pages: 119-126
Published online: 07 Feb 2014
AbstractforAssessment of Iron Overload in Very Young Children with Limited Thalassemia Care Resources in South China | Full Text | References | PDF (1.4 MB)
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Short Communications

Article
A New Hemoglobin Variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C]
Wu-Juan Cai, Xing-Mei Xie, Yong-Ling Zhang, Ru Li, Can Liao & Dong-Zhi Li
Pages: 127-129
Published online: 29 Jan 2014
AbstractforA New Hemoglobin Variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C] | Full Text | References | PDF (653.8 KB)
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Research Article

Article
Hb Ullevaal [β78(EF2)Leu→Val; HBB: c.235C>G], a New Hemoglobin Variant Interfering with Hb A1c Measurement Using a Cation Exchange High Performance Liquid Chromatography Method
Runa M. Grimholt, Åshild A. Sudmann, Armin P. Piehler, Petter Urdal & Olav Klingenberg
Pages: 130-132
Published online: 25 Nov 2013
AbstractforHb Ullevaal [β78(EF2)Leu→Val; HBB: c.235C>G], a New Hemoglobin Variant Interfering with Hb A1c Measurement Using a Cation Exchange High Performance Liquid Chromatography Method | Full Text | References | PDF (351.1 KB)
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Article
Hb A2-Konz [δ50(D1)Ser → Thr; HBD: c.151T > A]: a New δ Chain Hemoglobin Variant Characterized by Mass Spectrometry and High Performance Liquid Chromatography
Tchilabalo Dilezitoko Alayi, Alain Van Dorsselaer, Thomas Epting, Emmanuel Bissé & Christine Schaeffer-Reiss
Pages: 133-136
Published online: 29 Jan 2014
AbstractforHb A2-Konz [δ50(D1)Ser → Thr; HBD: c.151T > A]: a New δ Chain Hemoglobin Variant Characterized by Mass Spectrometry and High Performance Liquid Chromatography | Full Text | References | PDF (700.4 KB)
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Article
Hb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C)
Lauren Lubrano, Michael J. Donnelly, Gerald Sandler, James D. Hoyer, Kenneth C. Swanson, D. Brian Dawson & Jennifer L. Oliveira
Pages: 137-141
Published online: 16 Jan 2014
AbstractforHb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C) | Full Text | References | PDF (547.4 KB)
  • 139 Views
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Article
Case Report: Prenatal Diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a Family with an Adult Male Patient
Ru Li, Ting Wang, Xing-Mei Xie & Dong-Zhi Li
Pages: 142-145
Published online: 29 Jan 2014
AbstractforCase Report: Prenatal Diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a Family with an Adult Male Patient | Full Text | References | PDF (581.5 KB)
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Article
Detection of Hb Anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese Individuals
Ji-Wu Lou, Yi He, Yan-Hui Liu, Bai-Mao Zhong, Ying Zhao, Xiao-Xuan He & Dong-Zhi Li
Pages: 146-148
Published online: 29 Jan 2014
AbstractforDetection of Hb Anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese Individuals | Full Text | References | PDF (326.5 KB)
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Article
Severe α-Thalassemia Intermedia Due to a Compound Heterozygosity for the Highly Unstable Hb Adana (HBA2: c.179G>A) and a Novel Codon 24 (HBA2: c.75T>A) Mutation
Dewi Megawati, Ita M. Nainggolan, Maria Swastika, Susi Susanah, Johanes C. Mose, Alida R. Harahap & Iswari Setianingsih
Pages: 149-151
Published online: 18 Dec 2013
AbstractforSevere α-Thalassemia Intermedia Due to a Compound Heterozygosity for the Highly Unstable Hb Adana (HBA2: c.179G>A) and a Novel Codon 24 (HBA2: c.75T>A) Mutation | Full Text | References | PDF (251.9 KB)
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