Marianna Politou

Coexisting dysfibrinogenemia (gamma Arg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete).

A. Gialeraki, M. Neerman-Arbez, M. Politou, 2010, Thrombosis research.

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.

E. Terpos, D. Loukopoulos, G. Papanikolaou, 2000, Blood cells, molecules & diseases.

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin.

D. Loukopoulos, G. Papanikolaou, M. Politou, 2002, Blood cells, molecules & diseases.

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.

D. Loukopoulos, C. Camaschella, S. Bosio, 2001, Blood cells, molecules & diseases.

Correlation of single nucleotide polymorphisms in the promoter region of the ANXA5 (annexin A5) gene with recurrent miscarriages in women of Greek origin

K. Zoi, A. Pouliakis, M. Voulgarelis, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.