Hemoglobin, Volume 40, Issue 4 (2016)

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Hemoglobin, Volume 40, Issue 4 (2016)

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Original Article

Article
Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen
Margherita Vinciguerra, Cristina Passarello, Filippo Cassarà, Filippo Leto, Monica Cannata, Anna Crivello, Veronica Di Salvo, Aurelio Maggio & Antonino Giambona
Pages: 223-227
Published online: 02 Jun 2016
AbstractforHb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen | Full Text | References | PDF (575.7 KB)
  • 86 Views
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Article
High Frequency of Hb E-Saskatoon (HBB: c.67G > A) in Brazilians: A New Genetic Origin?
Sandrine C. Wagner, Juliana D. Lindenau, Simone M. de Castro, Ana Paula Santin, Carina F. Zaleski, Laura A. Azevedo, Ândrea K. C. Ribeiro dos Santos, Sidney E.B. dos Santos & Mara H. Hutz
Pages: 228-230
Published online: 02 Jun 2016
AbstractforHigh Frequency of Hb E-Saskatoon (HBB: c.67G > A) in Brazilians: A New Genetic Origin? | Full Text | References | PDF (206.3 KB)
  • 138 Views
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Article
Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling
Margherita Vinciguerra, Cristina Passarello, Filippo Leto, Anna Crivello, Maria Fustaneo, Filippo Cassarà, Monica Cannata, Aurelio Maggio & Antonino Giambona
Pages: 231-235
Published online: 03 Jun 2016
AbstractforCoinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling | Full Text | References | PDF (754.7 KB)
  • 195 Views
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Article
Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5′ Hypersensitive Site 4-Locus Control Region
Hossein Dehghani, Sepideh Ghobakhloo & Maryam Neishabury
Pages: 236-239
Published online: 05 Aug 2016
AbstractforElectromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5′ Hypersensitive Site 4-Locus Control Region | Full Text | References | PDF (274.4 KB)
  • 105 Views
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Article
Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?
Manousos E. Kambouris
Pages: 240-246
Published online: 02 Jun 2016
AbstractforPopulation Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile? | Full Text | References | PDF (641.2 KB)
  • 83 Views
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Article
A Program on Noninvasive Prenatal Diagnosis of α-Thalassemia in Mainland China: A Cost–Benefit Analysis
Yu Yang, Dong-Zhi Li & Ping He
Pages: 247-249
Published online: 07 Jul 2016
AbstractforA Program on Noninvasive Prenatal Diagnosis of α-Thalassemia in Mainland China: A Cost–Benefit Analysis | Full Text | References | PDF (138.3 KB)
  • 179 Views
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Article
Evaluation of the Relationship Between Hb F Levels and Nucleated Red Blood Cells with Morbidity in Non Transfusion-Dependent Thalassemia Patients
Mehran Karimi, Parisa Jooya, Sezaneh Haghpanah, Maral Mokhtari, Narges Rezaei, Maede Fath & Shirin Parand
Pages: 250-256
Published online: 22 May 2016
AbstractforEvaluation of the Relationship Between Hb F Levels and Nucleated Red Blood Cells with Morbidity in Non Transfusion-Dependent Thalassemia Patients | Full Text | References | PDF (371.1 KB)
  • 114 Views
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Short Communication

Rapid Communication
Hb Grifton [α87(F8)His→Pro; HBA1: C.263A > C (or HBA2)] Causes Abnormal Pulse Oximetry Measurements
Aubri M. Waters, Jason B. Caboot, Madeleine M. Verhovsek, David P. Harper & Melissa A. Forouhar
Pages: 257-259
Published online: 25 May 2016
AbstractforHb Grifton [α87(F8)His→Pro; HBA1: C.263A > C (or HBA2)] Causes Abnormal Pulse Oximetry Measurements | Full Text | References | PDF (254.1 KB)
  • 108 Views
  • 1 CrossRef citations
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Rapid Communication
Hb Tarrant [α126(H9)Asp→Asn; HBA2: c.379G > A (or HBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis
Ka Ling Rosalina Ip, Jason Chi-Chiu So, Man-Fai Law, Raymond S. M. Wong, Ho Chi Tam & Margaret H. L. Ng
Pages: 260-263
Published online: 31 May 2016
AbstractforHb Tarrant [α126(H9)Asp→Asn; HBA2: c.379G > A (or HBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis | Full Text | References | PDF (366.7 KB)
  • 143 Views
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Rapid Communication
Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation
Yu Yang, Dong-Zhi Li & Ping He
Pages: 264-266
Published online: 03 Jun 2016
AbstractforHb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation | Full Text | References | PDF (549.2 KB)
  • 110 Views
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Rapid Communication
Hb Savaria [α49(CE7)Ser→Arg; HBA2: c.150C > A]: A New Case and Complete Description
Thi Hai Yen Tran Houangkeo, Virginie Bodereau, Jean Riou & Serge Pissard
Pages: 267-269
Published online: 25 May 2016
AbstractforHb Savaria [α49(CE7)Ser→Arg; HBA2: c.150C > A]: A New Case and Complete Description | Full Text | References | PDF (527.6 KB)
  • 127 Views
  • 2 CrossRef citations
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Rapid Communication
Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India
Satyabrata Meher, Snehadhini Dehury, Pradeep Kumar Mohanty, Siris Patel, Chinmayee Pattanayak, Subhra Bhattacharya, Kishalaya Das & Biswanath Sarkar
Pages: 270-272
Published online: 02 Jun 2016
AbstractforHb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India | Full Text | References | PDF (500.3 KB)
  • 102 Views
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Rapid Communication
Report on Ten Years’ Experience of Premarital Hemoglobinopathy Screening at a Center in Antalya, Southern Turkey
Duran Canatan & Serpil Delibas
Pages: 273-276
Published online: 20 May 2016
AbstractforReport on Ten Years’ Experience of Premarital Hemoglobinopathy Screening at a Center in Antalya, Southern Turkey | Full Text | References | PDF (144.9 KB)
  • 362 Views
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Rapid Communication
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family
Sheng He, Li Lin, Yuan Wei, Biyan Chen, Shang Yi, Qiuli Chen, XiaoXia Qiu, Hongwei Wei, Guojian Li & Chenguang Zheng
Pages: 277-279
Published online: 05 Aug 2016
AbstractforIdentification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family | Full Text | References | PDF (340.3 KB)
  • 94 Views
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Rapid Communication
A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C
Turker Bilgen, Duran Canatan, Serpil Delibas & Ibrahim Keser
Pages: 280-282
Published online: 28 Jun 2016
AbstractforA Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C | Full Text | References | PDF (311.4 KB)
  • 232 Views
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Rapid Communication
Occurrence of the – –SEA, – –THAI and – –FILα-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, Thailand
Kobkorn Pongjantharasatien, Wansa Banyatsuppasin, Sonnarong Pounsawat & Sumalee Jindadamrongwech
Pages: 283-284
Published online: 05 Aug 2016
AbstractforOccurrence of the – –SEA, – –THAI and – –FILα-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, Thailand | Full Text | References | PDF (133.3 KB)
  • 225 Views
  • 5 CrossRef citations
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Rapid Communication
Prevalence of α+-Thalassemia in the Scheduled Tribe and Scheduled Caste Populations of Damoh District in Madhya Pradesh, Central India
Mendi P.S.S. Singh, Rasik B. Gupta, Rajiv Yadav, Ravendra K. Sharma & Rajasubramaniam Shanmugam
Pages: 285-288
Published online: 18 May 2016
AbstractforPrevalence of α+-Thalassemia in the Scheduled Tribe and Scheduled Caste Populations of Damoh District in Madhya Pradesh, Central India | Full Text | References | PDF (344.3 KB)
  • 117 Views
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Rapid Communication
The –(α)5.2 Deletion Detected in a Uruguayan Family: First Case Report in the Americas
Ana María Soler, Magdalena Schelotto, Natalia de Oliveira Mota, Roberta Dorta Ferreira, Maria de Fatima Sonati & Julio Abayubá da Luz
Pages: 289-292
Published online: 05 Aug 2016
AbstractforThe –(α)5.2 Deletion Detected in a Uruguayan Family: First Case Report in the Americas | Full Text | References | PDF (1,002.3 KB)
  • 46 Views
  • 1 CrossRef citations
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Rapid Communication
Is Vitamin C Supplementation in Patients with β-Thalassemia Major Beneficial or Detrimental?
Hadi Darvishi Khezri, Amir Emami Zeydi, Hassan Sharifi & Hossein Jalali
Pages: 293-294
Published online: 05 Aug 2016
AbstractforIs Vitamin C Supplementation in Patients with β-Thalassemia Major Beneficial or Detrimental? | Full Text | References | PDF (129.1 KB)
  • 270 Views
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