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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 2
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Original Article

Hemoglobin san diego/β→ thalassemia in a greek adult

D. Loukopoulos Department of Medicine, University of Athens Laikon General Hospital, Athens, 11527, Greece
,
C. Poyart Unite INSERM U.27, Hopital Foch, 92150, Suresnes, France
,
J. Delanoe-Garin Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
,
C. Matsis Department of Medicine, University of Athens Laikon General Hospital, Athens, 11527, Greece
,
N. Arous Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
,
J. Kister Unite INSERM U.27, Hopital Foch, 92150, Suresnes, France
,
A. Loutradi-Anagnostou Department of Medicine, University of Athens Laikon General Hospital, Athens, 11527, Greece
,
Y. Blouquit Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
,
Ph. Fessas Department of Medicine, University of Athens Laikon General Hospital, Athens, 11527, Greece
,
J. Thillet Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
,
J. Rosa Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
&
F. Galacteros Unite INSERM U.91, Hopital Henri Mondor, 94010, Creteil, France
 show all
Pages 143-159 | Received 08 May 1985, Accepted 10 Oct 1985, Published online: 07 Jul 2009

Citations (15)

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Read on this site (7)

Thein Hlaing Oo. (2021) Secondary erythrocytosis due to hemoglobin San Diego. Baylor University Medical Center Proceedings 34:1, pages 159-160.
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Amelia Oliveira, Dana Warcel, Nancy Huntley, Perla Eleftheriou & John B. Porter. (2016) Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and α-Thalassemia: A Clinical Update. Hemoglobin 40:2, pages 127-129.
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Paloma Ropero, Fernando A. González, Elena Cela, Cristina Beléndez, Beatriz Pérez, Cristina Seri, Emilia Fontanes, Ana Villegas & Joaquin Díaz-Mediavilla. (2013) Erythrocytosis in a Child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] Associated with a Spanish (δβ)0-Thalassemia. Hemoglobin 37:1, pages 48-55.
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Dima El-Sharkawi, Chris Fisher, Sachin Khambadkone, Adrian D. Stephens & John B. Porter. (2012) Secondary Erythrocytosis Due to Compound Homozygosity, but not Compound Heterozygosity, for Hb Luton and α-Thalassemia: A Family Study. Hemoglobin 36:1, pages 7-17.
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Cornelis L Harteveld, J.H Marc Groeneveld, Bastiaan van Dam, Peter Van Delft, Nicole Akkerman, Sandra Arkesteijn & Piero C. Giordano. (2005) Hb Zoeterwoude [β23(B5)Val → Ala)]: A New β-Globin Variant Found in Association with Erythrocytosis. Hemoglobin 29:1, pages 11-17.
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D. Williamson, D. J. Perry, K. Brown, J. V. Langdown & C. de Silva. (1995) Compound heterozygosity for two β chain variants Hb S [β6(A3)Glu → val] and the high affinity variant Hb san diego [β109(G11)Val → met]. Hemoglobin 19:1-2, pages 27-32.
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M. B. Coleman, J. G. Adams, A. M. Walker, M. W. Plonczynski, A. H. Harrell, J. A. Kark & G. P. Schechter. (1993) HB San Diego [β109(G11)VAL→MET] in an Iranian: Further Evidence for a Mutational Hot Spot at Position 109 of the β-Globin Gene. Hemoglobin 17:6, pages 543-545.
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Articles from other publishers (8)

Joshua Boster, Joseph Howells & Ryan Devine. (2019) Hemoglobin San Diego: An Uncommon Cause of Hereditary Erythrocytosis Discovered Incidentally in a Military Trainee. Military Medicine 184:5-6, pages e486-e488.
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P. Ropero, A. Villegas, A.F. Gonz�lez, E. Anguita, J. S�nchez, D.L. Carre�o, B. Arrizabalaga & L. Atuxta. (2000) Hb Johnstown [?109 (G11) Val?Leu]: Second case described and associated for the first time with ?0-thalassemia in two Spanish families. American Journal of Hematology 65:4, pages 298-301.
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George Vassilopoulos, Ioannis Papassotiriou, Ersi Voskaridou, Alexandra Stamoulakatou, Evangelos Premetis, Jean Kister, Michael Marden, Nathalie Griffon, Claude Poyart, Henri Wajcman, Frederic Galacteros & Dimitris Loukopoulos. (2008) Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β‐thalassaemia. British Journal of Haematology 91:3, pages 595-601.
Crossref
J. Rochette, R. Barnetson, L. Kiger, J. Kister, T. J. Littlewood, R. Webster, C. Poyart & S. L. Thein. (1994) Association of a novel high oxygen affinity haemoglobin variant with δβ thalassaemia. British Journal of Haematology 86:1, pages 118-124.
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Naoya Shibayama, Kiyohiro Imai, Hideki Morimoto & Satoshi Saigo. (2002) Oxygen equilibrium properties of asymmetric nickel(II)-iron(II) hybrid hemoglobin. Biochemistry 32:34, pages 8792-8798.
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Marie‐Pierre FONTAINE, Lars LINDQVIST, Yves BLOUQUIT & Jean ROSA. (2005) Structure dynamics of the hemoglobin mutants Hb Hôtel Dieu, HbG Philadelphia, HbJ Mexico, Hb St. Mandé and Hb San Diego, studied by nanosecond‐laser‐flash photolysis. European Journal of Biochemistry 186:3, pages 663-666.
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Said EL ANTRI, Christian ZENTZ & Bernard ALPERT. (2005) Implication of the α1β1 interface in the hemoglobin affinity changes. European Journal of Biochemistry 179:1, pages 165-168.
Crossref
J. Rochette, V. Baudin, B. Bohn, C. Poyart & H. Wajcman. (1986) Isolation of human haemoglobin variants with altered bohr effect. Journal of Chromatography A 369, pages 143-149.
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