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Πλοήγηση ανά Θέμα "CLINICAL-FEATURES"

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    • Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene 

      Daiou, C.; Christodoulou, K.; Xiromerisiou, G.; Panas, M.; Dardiotis, E.; Kladi, A.; Speletas, M.; Ntaios, G.; Papadimitriou, A.; Germenis, A.; Hadjigeorgiou, G. M. (2010)
      Phenotype of patients with the aprataxin gene mutation varies and according to previous studies, screening of aprataxin gene could be useful, once frataxin gene mutation is excluded in patients with normal GAA expansion ...

    • Enthesitis in psoriatic arthritis 

      Sakkas, L. I.; Alexiou, I.; Simopoulou, T.; Vlychou, M. (2013)
      Objectives: It is increasingly recognized that enthesitis in patients with psoriatic arthritis (PsA) is of clinical importance. We review data on the detection, assessment, and treatment of enthesitis and its related ...

    • Motor signs during the course of Alzheimer disease 

      Scarmeas, N.; Hadjigeorgiou, G. M.; Papadimitriou, A.; Dubois, B.; Sarazin, M.; Brandt, J.; Albert, M.; Marder, K.; Bell, K.; Honig, L. S.; Wegesin, D.; Stern, Y. (2004)
      Background: Motor signs (MOSIs) are common in Alzheimer disease (AD) and may be associated with rates of cognitive decline, mortality, and cost of care. Objective: To describe the progression and identify predictors of ...