Hemoglobin, Volume 41, Issue 4-6 (2017)

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Hemoglobin, Volume 41, Issue 4-6 (2017)

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Original Article

Article
Perinatal Maternal Mortality in Sickle Cell Anemia: Two Case Reports and Review of the Literature
Sanaa Rizk, Elizabeth D. Pulte, David Axelrod & Samir K. Ballas
Pages: 225-229
Published online: 28 Nov 2017
AbstractforPerinatal Maternal Mortality in Sickle Cell Anemia: Two Case Reports and Review of the Literature | Full Text | References | PDF (778 KB)
  • 426 Views
  • 6 CrossRef citations
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Article
Universal Screening Program in Pregnant Women and Newborns at-Risk for Sickle Cell Disease: First Report from Northern Italy
Mariachiara Lodi, Elena Bigi, Giovanni Palazzi, Lara Vecchi, Riccardo Morandi, Monica Setti, Silvana Borsari, Giuliano Bergonzini, Lorenzo Iughetti & Donatella Venturelli
Pages: 230-233
Published online: 12 Dec 2017
AbstractforUniversal Screening Program in Pregnant Women and Newborns at-Risk for Sickle Cell Disease: First Report from Northern Italy | Full Text | References | PDF (514.4 KB)
  • 201 Views
  • 8 CrossRef citations
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Article
HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene
Margherita Vinciguerra, Monica Cannata, Filippo Cassarà, Cristina Passarello, Filippo Leto, Giuseppina Calvaruso, Disma Renda, Aurelio Maggio & Antonino Giambona
Pages: 234-238
Published online: 24 Nov 2017
AbstractforHBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene | Full Text | References | PDF (886.2 KB)
  • 102 Views
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Article
Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene
John S. Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker & Barry Eng
Pages: 239-242
Published online: 28 Nov 2017
AbstractforCharacterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene | Full Text | References | PDF (518.7 KB)
  • 103 Views
  • 2 CrossRef citations
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Article
Prenatal Diagnosis and Molecular Analysis of a Large Novel Deletion (– –JS) Causing α0-Thalassemia
Jinru Cao, Shuzhen He, Yudong Pu, Jingjing Liu, Fuping Liu & Jun Feng
Pages: 243-247
Published online: 10 Nov 2017
AbstractforPrenatal Diagnosis and Molecular Analysis of a Large Novel Deletion (– –JS) Causing α0-Thalassemia | Full Text | References | PDF (1.4 MB)
  • 90 Views
  • 3 CrossRef citations
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Article
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program
Fan Jiang, Gui-Lan Chen, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Can Liao & Dong-Zhi Li
Pages: 248-253
Published online: 10 Nov 2017
AbstractforPre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program | Full Text | References | PDF (600.4 KB)
  • 124 Views
  • 24 CrossRef citations
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Article
Pseudoxanthoma Elasticum-Like in β-Thalassemia Major, a matter of α-Klotho and Parathyroid Hormone?
Alessandro Baldan, Andrea Giusti, Cristina Bosi, Cristina Malaventura, Gianluca Forni & Caterina Borgna-Pignatti
Pages: 254-259
Published online: 11 Dec 2017
AbstractforPseudoxanthoma Elasticum-Like in β-Thalassemia Major, a matter of α-Klotho and Parathyroid Hormone? | Full Text | References | PDF (712 KB) | Supplemental
  • 78 Views
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Article
Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand
Wansa Banyatsuppasin, Sumalee Jindadamrongwech, Anchalee Limrungsikul & Punnee Butthep
Pages: 260-266
Published online: 18 Dec 2017
AbstractforPrevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand | Full Text | References | PDF (724.3 KB)
  • 352 Views
  • 4 CrossRef citations
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Article
Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience
Ilham Youssry, Amina Abdel-Salam, Rania Ismail, Rayan Bou-Fakhredin, Rania Mohamed Samy, Fatma Ezz El-Deen & Ali T. Taher
Pages: 267-273
Published online: 18 Dec 2017
AbstractforEnhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience | Full Text | References | PDF (925.9 KB)
  • 191 Views
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Article
Hb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family
Yuan Zhao, Lv-Yin Huang, Fan Jiang, Jian-Ying Zhou, Xing-Mei Xie & Dong-Zhi Li
Pages: 274-277
Published online: 09 Jan 2018
AbstractforHb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family | Full Text | References | PDF (979.1 KB)
  • 47 Views
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Article
The Assessment and Sustainable Management of Sickle Cell Disease in the Indigenous Tharu Population of Nepal
Miles Marchand, Carson Gill, Armaan K. Malhotra, Carolyn Bell, Eric Busto, Monica D. McKeown, Abhiram Cherukupalli, Jordan Yeo, Brendan Arnold & Videsh Kapoor
Pages: 278-282
Published online: 09 Jan 2018
AbstractforThe Assessment and Sustainable Management of Sickle Cell Disease in the Indigenous Tharu Population of Nepal | Full Text | References | PDF (663.7 KB)
  • 387 Views
  • 6 CrossRef citations
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Short Communication

Rapid Communication
First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family
Nelson C.N. Chan, King-Ho Chow, Rico F.Y. Leung, Sequence S.H. Tang, Michelle F.W. Chiu, Rosalind Lie, Kelvin C.K. Cheng, Kin-Mang Lau, Natalie P.H. Chan & Margaret H.L. Ng
Pages: 283-285
Published online: 18 Oct 2017
AbstractforFirst Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family | Full Text | References | PDF (645.2 KB)
  • 115 Views
  • 1 CrossRef citations
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Rapid Communication
First Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese Family
Fan Jiang, Gui-Lan Chen, Jian-Ying Zhou & Dong-Zhi Li
Pages: 286-287
Published online: 18 Dec 2017
AbstractforFirst Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese Family | Full Text | References | PDF (330.3 KB)
  • 55 Views
  • 2 CrossRef citations
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Rapid Communication
Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese Family
Chuyun Cheng, Qi Peng, Siping Li, Lin Yang, Wenrui Li, Chunbao Rao & Xiaomei Lu
Pages: 288-290
Published online: 18 Dec 2017
AbstractforCoinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese Family | Full Text | References | PDF (557.3 KB)
  • 60 Views
  • 1 CrossRef citations
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Rapid Communication
Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait
Gui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou & Dong-Zhi Li
Pages: 291-292
Published online: 18 Dec 2017
AbstractforHb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait | Full Text | References | PDF (505.9 KB)
  • 56 Views
  • 3 CrossRef citations
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Rapid Communication
Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease
Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li
Pages: 293-296
Published online: 08 Nov 2017
AbstractforTwo α1-Globin Gene Point Mutations Causing Severe Hb H Disease | Full Text | References | PDF (644.2 KB)
  • 123 Views
  • 5 CrossRef citations
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Rapid Communication
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family
Sheng He, Qian Qin, Peng Huang, Shujie Zhang, Shang Yi, Li Lin, Yangjin Zuo, Qiuli Chen, Jianping Deng, Chenguang Zheng & Biyan Chen
Pages: 297-299
Published online: 21 Nov 2017
AbstractforCharacterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family | Full Text | References | PDF (783.8 KB)
  • 114 Views
  • 3 CrossRef citations
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Rapid Communication
Assessment of Cysteine Reactivity of Human Hemoglobin at Its Residue Level: A Mass Spectrometry-Based Approach
Amrita Mitra, Monita Muralidharan, Deepsikha Srivastava, Rajdeep Das, Vijay Bhat & Amit K. Mandal
Pages: 300-305
Published online: 06 Dec 2017
AbstractforAssessment of Cysteine Reactivity of Human Hemoglobin at Its Residue Level: A Mass Spectrometry-Based Approach | Full Text | References | PDF (903.4 KB)
  • 111 Views
  • 3 CrossRef citations
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Rapid Communication
A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T
Yuan Liang, Qi Peng, Miao Li, Siping Li, Wenrui Li & Xiaomei Lu
Pages: 306-307
Published online: 18 Dec 2017
AbstractforA Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T | Full Text | References | PDF (507.8 KB)
  • 41 Views
  • 2 CrossRef citations
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Rapid Communication
First Cases of Hb Agrinio Described in Patients from the Republic of Macedonia
Marija Dimishkovska, Maja Kuzmanovska, Svetlana Kocheva, Kata Martinova, Oliver Karanfilski, Zlate Stojanoski & Dijana Plaseska-Karanfilska
Pages: 308-310
Published online: 08 Dec 2017
AbstractforFirst Cases of Hb Agrinio Described in Patients from the Republic of Macedonia | Full Text | References | PDF (590.3 KB)
  • 95 Views
  • 2 CrossRef citations
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Rapid Communication
A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh
Abdul Aziz, Sudipta A. Das, Waqar A. Khan, Salma Sadiya, Bilquis Banu, Golam Sarwardi & Rowshon Z. Luna
Pages: 311-313
Published online: 09 Jan 2018
AbstractforA Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh | Full Text | References | PDF (509.3 KB)
  • 55 Views
  • 1 CrossRef citations
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Rapid Communication
Hb Mozhaisk [β92(F8)His→Arg; HBB: c.278A>G] as a De Novo Mutation in a Child of Mixed Ethnic Origins
Elena Benzoni, Valentina Giannone, Laura Michetti, Manuela Seia, Laura Cavalleri & Cristina Curcio
Pages: 314-316
Published online: 09 Jan 2018
AbstractforHb Mozhaisk [β92(F8)His→Arg; HBB: c.278A>G] as a De Novo Mutation in a Child of Mixed Ethnic Origins | Full Text | References | PDF (721.8 KB)
  • 69 Views
  • 1 CrossRef citations
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Rapid Communication
Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant
Aparna A. Bhanushali, Kumari Himani, Pradeep K. Patra & Bibhu R. Das
Pages: 317-320
Published online: 09 Jan 2018
AbstractforHb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant | Full Text | References | PDF (384.2 KB)
  • 77 Views
  • 7 CrossRef citations
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