Citations (23)
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Hua Jiang, Jin-Mei Yan, Jian Li, Xing-Mei Xie & Dong-Zhi Li. (2016) Diagnostic Dilemma of Hb Perth [β32(B14)Leu→Pro; HBB: c.98T > C] in Mainland China. Hemoglobin 40:3, pages 202-205.
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Elisabeth Saller, Kamran Moradkhani, Fabrizio Dutly, Isabelle Vinatier, Claude Préhu, Hannes Frischknecht & Michel Goossens. (2012) Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels. Hemoglobin 36:2, pages 177-182.
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Piero C. Giordano, Margaretha Bakker-Verwij & Cornelis L. Harteveld. (2009) Frequency of α-Globin Gene Triplications and Their Interaction with β-Thalassemia Mutations. Hemoglobin 33:2, pages 124-131.
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Cornelis L. Harteveld, Willem C.H. van Helden, George L. Boxma, Peter van Delft, Margaretha Bakker-Verweij, Henri Wajcman, Isabelle Zanella-Cleon, Michel Becchi & Piero C. Giordano. (2007) Hb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype. Hemoglobin 31:3, pages 325-332.
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Claude Préhu, Jean Riou & Henri Wajcman. (2007) Hb Barika [α42(C7)Tyr→His (α2)] Leads to an α+-Thalassemia-like Syndrome. Hemoglobin 31:1, pages 17-22.
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Ioannis Papassotiriou, Alexandra Stamoulakatou, Henri Wajcman, Jean Kister, Gerasimos Dimisianos, Christina Lazaropoulou, Ino Kanavaki, Efstathios Vavourakis, Antonios Kattamis, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2006) Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a β+-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family. Hemoglobin 30:4, pages 409-418.
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Antonino Giambona, Margherita Vinciguerra, Filippo Cassarà, Rita Li Muli, Filippo Leto, Cristina Passarello, Henri Wajcman & Aurelio Maggio. (2006) Hb Marineo [β70(E14)Ala→Val]: A Silent Hemoglobin Variant with a Mutation Within the Heme Pocket. Hemoglobin 30:2, pages 139-148.
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Valérie Bardet, Mircea Adam, Jeanine Yvart, Henri Wajcman, Frédéric Galacteros & Rémi Favier. (2006) Hb Calais [β76(E20)Ala→Pro]: A Family Study of a Variant With Decreased Oxygen Affinity. Hemoglobin 30:1, pages 35-38.
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Henri Wajcman, Josiane Bardakdjian‐Michau, Jean Riou, Claude Préhu, Jean Kister, Véronique Baudin‐Creuza, Danielle Promé, Suzy Richelme‐David, Jean Luc Harousseau & Frédéric Galactéros. (2003) Two New Hemoglobin Variants with Increased Oxygen Affinity: Hb Nantes [β34(B16)Val → Leu] and Hb Vexin [β116(G18)His → Leu]. Hemoglobin 27:3, pages 191-199.
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Claude Préhu, Mohamed Rhabbour, Jean Claude Netter, Mathias Denier, Jean Riou, Frédéric Galactéros & Henri Wajcman. (2003) Hb F‐M‐Osaka [Gγ63(E7)His→Tyr] in a Newborn from Southwest France. Hemoglobin 27:1, pages 27-30.
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Articles from other publishers (13)
Izmarie Poventud-Fuentes, Emily Garnett, Beverly Vispo, M. Tarek Elghetany & Sridevi Devaraj. (2021) Hemoglobin fractionation by Sebia Capillarys 2 Flex Piercing System as primary method for evaluation of hemoglobinopathies. Clinica Chimica Acta 519, pages 193-197.
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Constantinos C. LoucariPetros PatsaliThamar B. van DijkCoralea StephanouPanayiota PapasavvaMaria ZantiRyo Kurita, Yukio Nakamura, Soteroulla ChristouMaria SitarouSjaak PhilipsenCarsten W. LedererMarina Kleanthous. (2018) Rapid and Sensitive Assessment of Globin Chains for Gene and Cell Therapy of Hemoglobinopathies. Human Gene Therapy Methods 29:1, pages 60-74.
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Jun-Hui Wan, Pei-Ling Tian, Wei-Hao Luo, Bing-Yi Wu, Fu Xiong, Wan-Jun Zhou, Xiang-Cai Wei & Xiang-Min Xu. (2012) Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography. Journal of Chromatography B 901, pages 53-58.
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Henri Wajcman & Jean Riou. (2009) Globin chain analysis: An important tool in phenotype study of hemoglobin disorders. Clinical Biochemistry 42:18, pages 1802-1806.
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M. Nagara, C. Alba-Sauviat, D. Simeon, M.-F. Gaudeau-Toussaint, F. Fontvielle & G. Faucher. (2009) L’hémoglobinose C homozygote : à propos d’un cas de découverte fortuite. Immuno-analyse & Biologie Spécialisée 24:4, pages 210-216.
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Isabelle Zanella-Cleon, Michel Becchi, Philippe Lacan, Piero C Giordano, Henri Wajcman & Alain Francina. (2008) Detection of a Thalassemic α-Chain Variant (Hemoglobin Groene Hart) by Reversed-Phase Liquid Chromatography. Clinical Chemistry 54:6, pages 1053-1059.
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Laura Manca & Bruno Masala. (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life 60:2, pages 94-111.
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R. B. Colah, R. Surve, P. Sawant, E. D’Souza, K. Italia, S. Phanasgaonkar, A. H. Nadkarni & A. C. Gorakshakar. (2007) HPLC studies in hemoglobinopathies. The Indian Journal of Pediatrics 74:7, pages 657-662.
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C Préhu, J Riou, J Henthorn & H Wajcman. (2007) A New Silent β Chain Variant: Hb Hounslow [β80(EF4)Asn→Tyr]. Balkan Journal of Medical Genetics 10:1, pages 29-32.
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Laura Manca, Marcella Corda, Mariagiuseppina Pellegrini, Antonella Fais, Eleftherios Hadjisterkotis, Andràs Nàhlik, Adriana Basile, Pasquale Ferranti & Bruno Masala. (2007) Structure and function of sheep hemoglobin Chios: A novel allele at the HBBB locus with two Lys→Arg substitutions at positions β66(E10) and β144(HC1). Comparative Biochemistry and Physiology Part D: Genomics and Proteomics 2:1, pages 84-90.
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J. Bardakdjian-Michau. (2007) Hémoglobines. EMC - Biologie médicale 2:4, pages 1-5.
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Ioannis Papassotiriou, Joanne Traeger-Synodinos, Michael C. Marden, Jean Kister, Dimitra Liapi, Danielle Prome, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2005) The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia. Blood Cells, Molecules, and Diseases 34:3, pages 229-234.
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Jean Kister, Véronique Baudin-Creuza, Laurent Kiger, Claude Préhu, Ioannis Papassotiriou, Jean Riou, Frédéric Galactéros & Henri Wajcman. (2005) Hb Montfermeil [β 130(H8) Tyr→Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule. Blood Cells, Molecules, and Diseases 34:2, pages 166-173.
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