|1.||Rombos, Ioannis: 1 article (01/2010)|
|2.||Tzanetea, Revekka: 1 article (01/2010)|
|3.||Papassotiriou, Ioannis: 1 article (01/2010)|
|4.||Konstantopoulos, Kostas: 1 article (01/2010)|
|5.||Kalotychou, Vassiliki: 1 article (01/2010)|
01/01/2010 - "The molecular defect for erythrocytosis was detected together with the rare Hb Olympia (HBB:c.61G>A) variant. "
11/01/1996 - "Structural modifications affecting position beta 20(B2) have been demonstrated to be responsible for a high oxygen affinity and polycythemia in Hb Olympia (Val-->Met) and Hb Trölhattan (Val-->Glu). "
07/01/1994 - "This mutation occurs at the same position as Hb Olympia [beta 20(B2)Val-->Met], another variant associated with erythrocytosis due to increased oxygen affinity. "
01/01/1978 - "Environmental modification of gene expression: iron deficiency masks erythrocytosis in a female with hemoglobin Olympia."
01/01/2010 - "Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature."
07/01/1985 - "Iron overload associated with Hemoglobin Olympia."
09/01/1984 - "Iron overload in three generations of a family with hemoglobin Olympia."
|4.||Hemochromatosis (Bronze Diabetes)
09/01/1984 - "The findings in this family are consistent with an increase in iron absorption due to the consequences of Hemoglobin Olympia and the heterozygous state for hemochromatosis (allele for hemochromatosis associated with HLA-A3, B7) or the presence in the family pedigree of three different alleles for hemochromatosis (alleles for hemochromatosis associated with HLA-A3. "