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Browsing by Subject "familial disease"

Now showing items 1-4 of 4

    • Intrafamilial spread of hepatitis B virus infection in Greece 

      Zervou, E. K.; Gatselis, N. K.; Xanthi, E.; Ziciadis, K.; Georgiadou, S. P.; Dalekos, G. N. (2005)
      Objective: No study has investigated the intrafamilial spread of hepatitis B virus (HBV) in Greece. We conducted a 9-year prospective study to determine the rate of HBV spread in family members when a member is identified ...

    • Mutated α-synuclein gene in two greek kindreds with familial pd: Incomplete penetrance? 

      Papadimitriou, A.; Veletza, V.; Hadjigeorgiou, G. M.; Patrikiou, A.; Hirano, M.; Anastasopoulos, I. (1999)
      The G209A mutation in the α-synuclein gene has been associated with autosomal dominant PD (ADPD) in a family from Contursi, Italy, and three apparently unrelated Greek families. Several groups around the world failed to ...

    • Primary biliary cirrhosis: Family stories 

      Smyk, D.; Cholongitas, E.; Kriese, S.; Rigopoulou, E. I.; Bogdanos, D. P. (2011)
      Primary biliary cirrhosis (PBC) is a chronic immune-mediated cholestatic liver disease of unknown aetiology which affects mostly women in middle age. Familial PBC is when PBC affects more than one member of the same family, ...

    • A probable role of copper in the comorbidity in Wilson's and Creutzfeldt-Jakob's Diseases: A case report 

      Koutsouraki E., Michmizos D., Patsi O., Tzartos J., Spilioti M., Arnaoutoglou M., Tsolaki M. (2020)
      Background: To the best of our knowledgedd, there is currently no case in the literature reporting the comorbidity of Wilson's and Creutzfeldt-Jakob disease (CJD), linked through copper. Case presentation: A 44-year-old ...