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Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family.
Papassotiriou I, Stamoulakatou A, Wajcman H, Kister J, Dimisianos G, Lazaropoulou C, Kanavaki I, Vavourakis E, Kattamis A, Kanavakis E, Traeger-Synodinos J. Papassotiriou I, et al. Among authors: kattamis a. Hemoglobin. 2006;30(4):409-18. doi: 10.1080/03630260600867842. Hemoglobin. 2006. PMID: 16987796
Plasma neutrophil gelatinase-associated lipocalin levels are markedly increased in patients with non-transfusion-dependent thalassemia: Lack of association with markers of erythropoiesis, iron metabolism and renal function.
Patsaoura A, Tatsi E, Margeli A, Kanavaki I, Delaporta P, Kyriakopoulou D, Kouraklis-Symeonidis A, Kattamis A, Papassotiriou I. Patsaoura A, et al. Among authors: kattamis a. Clin Biochem. 2014 Aug;47(12):1060-4. doi: 10.1016/j.clinbiochem.2014.03.017. Epub 2014 Apr 8. Clin Biochem. 2014. PMID: 24721683
Growth and development in children with thalassaemia major.
Kattamis C, Liakopoulou T, Kattamis A. Kattamis C, et al. Among authors: kattamis a. Acta Paediatr Scand Suppl. 1990;366:111-7; discussion 118. doi: 10.1111/j.1651-2227.1990.tb11611.x. Acta Paediatr Scand Suppl. 1990. PMID: 2206002 Review. No abstract available.
218 results