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Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to α-thalassemia intermedia, when in trans to a single α-globin gene deletion.
Kattamis A, Delaporta P, Fylaktou I, Vrettou C, Kyriakopoulou D, Stamoulakatou A, Papassotiriou I, Kanavakis E, Traeger-Synodinos J. Kattamis A, et al. Among authors: delaporta p. Hemoglobin. 2015;39(1):55-7. doi: 10.3109/03630269.2014.981827. Epub 2014 Dec 5. Hemoglobin. 2015. PMID: 25476779
Cystatin C levels in patients with beta-thalassemia during deferasirox treatment.
Papassotiriou I, Margeli A, Hantzi E, Delaporta P, Sergounioti A, Goussetis E, Ladis V, Kattamis A. Papassotiriou I, et al. Among authors: delaporta p. Blood Cells Mol Dis. 2010 Mar 15;44(3):152-5. doi: 10.1016/j.bcmd.2010.01.001. Epub 2010 Jan 29. Blood Cells Mol Dis. 2010. PMID: 20110177
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: delaporta p. 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
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