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Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.
Skarmoutsou C, Papassotiriou I, Traeger-Synodinos J, Stamou H, Ladis V, Metaxotou-Mavrommati A, Stamoulakatou A, Kanavakis E. Skarmoutsou C, et al. Among authors: ladis v. Haematologica. 2003 Jun;88(6):631-6. Haematologica. 2003. PMID: 12801838
Impaired oxygen kinetics in beta-thalassaemia major patients.
Vasileiadis I, Roditis P, Dimopoulos S, Ladis V, Pangalis G, Aessopos A, Nanas S. Vasileiadis I, et al. Among authors: ladis v. Acta Physiol (Oxf). 2009 Jul;196(3):357-63. doi: 10.1111/j.1748-1716.2008.01937.x. Epub 2008 Nov 27. Acta Physiol (Oxf). 2009. PMID: 19040710 Clinical Trial.
The impact of neocyte transfusion in the management of thalassaemia.
Spanos T, Ladis V, Palamidou F, Papassotiriou I, Banagi A, Premetis E, Kattamis C. Spanos T, et al. Among authors: ladis v. Vox Sang. 1996;70(4):217-23. doi: 10.1111/j.1423-0410.1996.tb01330.x. Vox Sang. 1996. PMID: 9123927 Clinical Trial.
Growth and management of short stature in thalassaemia major.
Theodoridis C, Ladis V, Papatheodorou A, Berdousi H, Palamidou F, Evagelopoulou C, Athanassaki K, Konstantoura O, Kattamis C. Theodoridis C, et al. Among authors: ladis v. J Pediatr Endocrinol Metab. 1998;11 Suppl 3:835-44. J Pediatr Endocrinol Metab. 1998. PMID: 10091154
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