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Volume 36, Number 6, August 2012

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Original Article

Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a New α-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases
pp. 517-525(9)
Authors: Bento, Celeste; Oliveira, Ana Catarina; Neves, Joana; Gameiro, Mariline; Cunha, Elizabete; Coucelo, Margarida; Costa, Ricardo Marques; Barbot, José; Costa, Emilia; Fernández-Lago, Carlos; Ribeiro, M. Leticia

Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases
pp. 526-532(7)
Authors: de la Fuente-Gonzalo, Felix; Baiget, Montserrat; Badell, Isabel; Ricard, Pilar; Vinuesa, Lara; Martínez-Nieto, Jorge; Ropero, Paloma; Villegas, Ana; González, Fernando A.; Díaz-Mediavilla, Joaquin; The Erythropathology Spanish Group,

Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βS Chromosomes
pp. 533-544(12)
Authors: Ben Mustapha, Maha; Moumni, Imen; Zorai, Amine; Douzi, Kaïs; Ghanem, Abderraouf; Abbes, Salem

Two Assays to Evaluate Potential Genotoxic Effects of Hydroxyurea in Sickle Cell Disease Patients
pp. 545-554(10)
Authors: Rodríguez, Anar; Kouegnigan, Leonard; Ferster, Alina; Cotton, Frédéric; Duez, Pierre

Study of Serum Hepcidin in Hereditary Hemolytic Anemias
pp. 555-570(16)
Authors: El Beshlawy, Amal; Alaraby, Ibrahim; Abdel Kader, Mohamed S.E.M.; Ahmed, Dina H.; Abdelrahman, Hossam E.M.

A Single-Tube Multiplex Gap-Polymerase Chain Reaction for the Detection of Eight β-Globin Gene Cluster Deletions Common in Southeast Asia
pp. 571-580(10)
Authors: Tritipsombut, Jaruwan; Phylipsen, Marion; Viprakasit, Vip; Chalaow, Nipon; Sanchaisuriya, Kanokwan; Giordano, Piero C.; Fucharoen, Supan; Harteveld, Cornelis L.

Short Communication

A New ATRX Mutation in a Patient With Acquired α-Thalassemia Myelodysplastic Syndrome
pp. 581-585(5)
Authors: Herbaux, Charles; Badens, Catherine; Guidez, Stéphanie; Lacoste, Caroline; Maboudou, Patrice; Rose, Christian

A Novel β0-Thalassemia Frameshift Mutation: [HBB:c.216delT]
pp. 586-588(3)
Authors: Konialis, Christopher; Hagnefelt, Birgitta; Sevastidou, Sophia; Pispili, Katerina; Pangalos, Constantinos

α0-Thalassemia Trait with Normal Red Cell Indices: A Report of Two Cases
pp. 589-591(3)
Authors: Liao, Can; Li, Dong-Zhi

Influence of BCL11A, HBS1L-MYB, HBBP1 Single Nucleotide Polymorphisms and the HBG2 XmnI Polymorphism On Hb F Levels
pp. 592-599(8)
Authors: Roy, Papai; Bhattacharya, Gargi; Mandal, Amrita; Dasgupta, Uma B.; Banerjee, Debasis; Chandra, Sarmila; Das, Manikanchan

Thrombosis in Hb Taybe [codons 38/39 (-ACC) (α1)]
pp. 600-604(5)
Authors: Juul, Maja Bech; Vestergaard, Hanne; Petersen, Jesper; Frederiksen, Henrik

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