Πλοήγηση ανά Συγγραφέα "Kioumi, A."
-
Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
Speletas, M.; Kioumi, A.; LouleS, G.; Hytiroglou, P.; Tsitouridis, J.; Christakis, J.; GermeniS, A. E. (2008)Mutations in the SLC40Al gene result in a dominant genetic disorder [ferroportin disease; hereditary hemochromatosis type (HH) IV], characterized by iron overload with two different clinical manifestations, normal transferrin ... -
Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV (vol 40, pg 353, 2008)
Speletas, M.; Kioumi, A.; Loules, G.; Hytiroglou, P.; Tsitouridis, J.; Christakis, J.; Germenis, A. E. (2013) -
Analysis of SLC40A1(Ferroportin 1) gene at mrna level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
Speletas, M.; Kioumi, A.; Loules, G.; Kalala, F.; Katodritou, E.; Tsitouridis, I.; Hytiroglou, P.; Christakis, J.; Korantzis, I.; Germenis, A. (2007) -
Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia
Tsantoula, F.; Kioumi, A.; Germenis, A. E.; Speletas, M. (2014)A 2-year-old female was presented with high levels of serum ferritin (890 ng/mL) in a routine blood test. Clinical and laboratory investigations excluded the presence of iron overload and secondary causes of hyperferritinemia. ... -
Influence of common thrombophilia polymorphisms on the thrombosis risk in patients with JAK2-V617F-positive myeloproliferative neoplasms
Giamouris, V.; Befani, M.; Papadakis, E.; Mandala, E.; Papadoulis, N.; Karamagiolis, S.; Gastari, V.; Verrou, E.; Katodritou, E.; Lafioniatis, S.; Kartasis, Z.; Magiannis, K.; Marinaki, P.; Tsioni, K.; Kioumi, A.; Germenis, A. E.; Speletas, M. (2012) -
Reply to: "SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting"
Speletas, M.; Kioumi, A.; Germenis, A. E. (2013) -
SLC40A1-R178G mutation and ferroportin disease
Speletas, M.; Onoufriadis, E.; Kioumi, A.; Germenis, A. E. (2011) -
TNFRSF13B GENE EXPRESSION AND MOLECULAR ANALYSIS IN B-CELL CHRONIC LYMPHOPROLIFERATIVE DISORDERS
Speletas, M.; Mamara, A.; Kalala, F.; Liadaki, K.; Papadoulis, N.; Kioumi, A.; Giannakoulas, N.; Lafioniatis, S.; Loukidis, K.; Matsouka, P.; Kartasis, Z.; Germenis, A. (2009)