Hemoglobin, Volume 31, Issue 2 (2007)

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Hemoglobin, Volume 31, Issue 2 (2007)

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Article
Hb J-CAPE TOWN [α92(FG4)Arg→Gln (α1), CGG→CAG] in Southern Italy Found in a Patient with Erythrocytosis
Leonilde Pagano, Angela Flagiello, Roberta Tedesco, Massimiliano Ammirabile, Filiberto Pollio, Luciano Prossomariti, Antonino Giambona, Cristina Passarello & Piero Pucci
Pages: 113-120
Published online: 07 Jul 2009
AbstractforHb J-CAPE TOWN [α92(FG4)Arg→Gln (α1), CGG→CAG] in Southern Italy Found in a Patient with Erythrocytosis | Full Text | References | PDF (117 KB)
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Article
Molecular Basis of Thalassemia in Qatar
Aisha Al-Obaidli, Mowafak Hamodat, Zainab Fawzi, Mohamed Abu-Laban, Nathalie Gerard & Rajagopal Krishnamoorthy
Pages: 121-127
Published online: 07 Jul 2009
AbstractforMolecular Basis of Thalassemia in Qatar | Full Text | References | PDF (74.9 KB)
  • 164 Views
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Article
Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening
Barry Eng, Lynda Walker, Lisa M. Nakamura, Carolyn Hoppe, Mahin Azimi, Helen Lee & John S. Waye
Pages: 129-134
Published online: 07 Jul 2009
AbstractforThree New β-Globin Gene Promoter Mutations Identified Through Newborn Screening | Full Text | References | PDF (96 KB)
  • 206 Views
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Article
Two New α-Thalassemia Frameshift Mutations
Hong-Yuang Luo, Adeboye H. Adewoye, Monika Pilichowska, Michael Yunlong Li, Raveen K. Basran, Martin H. Steinberg & David H.K. Chui
Pages: 135-139
Published online: 07 Jul 2009
AbstractforTwo New α-Thalassemia Frameshift Mutations | Full Text | References | PDF (134.3 KB)
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Article
Genotypic Correlation Between Six Common β-Thalassemia Mutations and the XmnI Polymorphism in the Moroccan Population
Imane Agouti, Catherine Badens, Ahmed Abouyoub, Mohamed Khattab, Fouad Sayah, Amina Barakat & Mohcine Bennani
Pages: 141-149
Published online: 07 Jul 2009
AbstractforGenotypic Correlation Between Six Common β-Thalassemia Mutations and the XmnI Polymorphism in the Moroccan Population | Full Text | References | PDF (106.3 KB)
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Short Communication

Article
Three New α-Globin Variants: Hb Itapira [α30(B11)Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11)Glu→Ala (α1)] and Hb Boa Esperança [α16(A14)Lys→Thr (α2)]
Susan E. Costa Jorge, Elza M. Kimura, Denise M. Oliveira, Satie Ogo, Dulcinéia M. Albuquerque, Fernando F. Costa & Maria de Fátima Sonati
Pages: 151-157
Published online: 07 Jul 2009
AbstractforThree New α-Globin Variants: Hb Itapira [α30(B11)Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11)Glu→Ala (α1)] and Hb Boa Esperança [α16(A14)Lys→Thr (α2)] | Full Text | References | PDF (264.5 KB)
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Article
Two New β0-Thalassemic Mutations: A Deletion (−CC) at Codon 142 or Overlapping Codons 142-143, and an Insertion (+T) at Codon 45 or Overlapping Codons 44-45/45-46 of the β-Globin Gene
Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina
Pages: 159-165
Published online: 07 Jul 2009
AbstractforTwo New β0-Thalassemic Mutations: A Deletion (−CC) at Codon 142 or Overlapping Codons 142-143, and an Insertion (+T) at Codon 45 or Overlapping Codons 44-45/45-46 of the β-Globin Gene | Full Text | References | PDF (122.7 KB)
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Article
The Rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in Combination with an α Gene Triplication Found in a Dutch Patient During Her First Pregnancy Examination
Piero C. Giordano, Akosua Addo-Daaku, Margaretha J. Sander, Irene van Rooijen-Nijdam, Peter van Delft, Cornelis L. Harteveld & Peter J.M.J. Kok
Pages: 167-171
Published online: 07 Jul 2009
AbstractforThe Rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in Combination with an α Gene Triplication Found in a Dutch Patient During Her First Pregnancy Examination | Full Text | References | PDF (104 KB)
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Article
A Moderately Severe α-Thalassemia Condition Resulting From a Combination of the α2 Polyadenylation Signal (AATAAA→AATA– –) Mutation and a 3.7 Kb α Gene Deletion in an Australian Family
John F. Prior, Erna Lim, Neela Lingam, John L. Raven & Jill Finlayson
Pages: 173-177
Published online: 07 Jul 2009
AbstractforA Moderately Severe α-Thalassemia Condition Resulting From a Combination of the α2 Polyadenylation Signal (AATAAA→AATA– –) Mutation and a 3.7 Kb α Gene Deletion in an Australian Family | Full Text | References | PDF (134.5 KB)
  • 106 Views
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Article
The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant
Piero C. Giordano, Sonja Zweegman, Nicole Akkermans, Sandra G.J. Arkesteijn, Peter van Delft, Florens G.A. Versteegh, Henri Wajcman & Cornelis L. Harteveld
Pages: 179-182
Published online: 07 Jul 2009
AbstractforThe First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant | Full Text | References | PDF (94.6 KB)
  • 169 Views
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Article
Hematological and Molecular Characteristics of Hb Sarrebourg [β131(H9)Gln→Arg (CAG→CGG)] Found in a Spanish Family
David Beneitez Pastor, Alícia Carrera, Joan Ramón Duran-Suárez, Maria Antonia Durán Pastor, Federico Álvarez Vinent & Carmen Melich
Pages: 183-185
Published online: 07 Jul 2009
AbstractforHematological and Molecular Characteristics of Hb Sarrebourg [β131(H9)Gln→Arg (CAG→CGG)] Found in a Spanish Family | Full Text | References | PDF (68.5 KB)
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Second Titus H.J. Huisman Memorial Symposium: Recent Advances in Hemoglobinopathy, May 8–9, 2006, Adana, Turkey

Article
Professor Titus H.J. Huisman and the Medical College of Georgia
Russell R. Moores
Pages: 187-191
Published online: 07 Jul 2009
First Page PreviewforProfessor Titus H.J. Huisman and the Medical College of Georgia | Full Text | PDF (50.6 KB)
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Article
Dominantly Inherited β-Thalassemia
Georgi D. Efremov
Pages: 193-207
Published online: 07 Jul 2009
AbstractforDominantly Inherited β-Thalassemia | Full Text | References | PDF (216.9 KB)
  • 356 Views
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Article
Sickle Cell Disease: A Multigenic Perspective of a Single Gene Disorder
Abdullah Kutlar
Pages: 209-224
Published online: 07 Jul 2009
AbstractforSickle Cell Disease: A Multigenic Perspective of a Single Gene Disorder | Full Text | References | PDF (133.8 KB)
  • 378 Views
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Article
Molecular Basis of β-Thalassemia and Other Hemoglobinopathies in Bulgaria: An Update
Georgi H. Petkov & Georgi D. Efremov
Pages: 225-232
Published online: 07 Jul 2009
AbstractforMolecular Basis of β-Thalassemia and Other Hemoglobinopathies in Bulgaria: An Update | Full Text | References | PDF (76.5 KB)
  • 79 Views
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Article
The Molecular Pathology of β-Thalassemia in Turkey: The Boğaziçi University Experience
A. Nazı Başak
Pages: 233-241
Published online: 07 Jul 2009
AbstractforThe Molecular Pathology of β-Thalassemia in Turkey: The Boğaziçi University Experience | Full Text | References | PDF (152.4 KB)
  • 312 Views
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Article
Diagnostic Approach to Hemoglobinopathies
Ferdane Kutlar
Pages: 243-250
Published online: 07 Jul 2009
AbstractforDiagnostic Approach to Hemoglobinopathies | Full Text | References | PDF (134.9 KB)
  • 879 Views
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Article
Stem Cell Transplantation in Hemoglobinopathies
M. Akif Yesilipek
Pages: 251-256
Published online: 07 Jul 2009
AbstractforStem Cell Transplantation in Hemoglobinopathies | Full Text | References | PDF (101.4 KB)
  • 126 Views
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Article
Results From The North Cyprus Thalassemia Prevention Program
Gülsen Bozkurt
Pages: 257-264
Published online: 07 Jul 2009
AbstractforResults From The North Cyprus Thalassemia Prevention Program | Full Text | References | PDF (93.2 KB)
  • 472 Views
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Article
Hb H (β4) Disease in Çukurova, Southern Turkey
Mehmet Akif Çürük
Pages: 265-271
Published online: 07 Jul 2009
AbstractforHb H (β4) Disease in Çukurova, Southern Turkey | Full Text | References | PDF (68.6 KB)
  • 126 Views
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Article
Preliminary Data on Preimplantation Genetic Diagnosis for Hemoglobinopathies in Turkey
Filiz Zeren, Ahmet Genç & Mehmet Akif Çürük
Pages: 273-277
Published online: 07 Jul 2009
AbstractforPreliminary Data on Preimplantation Genetic Diagnosis for Hemoglobinopathies in Turkey | Full Text | References | PDF (59.4 KB)
  • 86 Views
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Article
A Review of Cis-Trans Interplay Between DNA Sequences 5′ to the Gγ- and β-Globin Genes Among Hb F-Malta-I Heterozygotes/Homozygotes and β-Thalassemia Homozygotes/Compound Heterozygotes, and the Effects of Hydroxyurea on the Hb F/F-Erythrocyte; the Need for Large Multicenter Trials
Alex E. Felice, Joseph Borg, Monica Pizzuto, Wilhelmina Cassar, Ruth Galdies, Stephanie Bezzina Wettinger, Svetlana Pulis, Gary J. Hunter, Mary R. Caruana, Mario Farrugia & Christian A. Scerri
Pages: 279-288
Published online: 07 Jul 2009
AbstractforA Review of Cis-Trans Interplay Between DNA Sequences 5′ to the Gγ- and β-Globin Genes Among Hb F-Malta-I Heterozygotes/Homozygotes and β-Thalassemia Homozygotes/Compound Heterozygotes, and the Effects of Hydroxyurea on the Hb F/F-Erythrocyte; the Need for Large Multicenter Trials | Full Text | References | PDF (152.8 KB)
  • 56 Views
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