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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 12 results:
Author Title Type [ Year(Asc)]
Filters: Author is Bougea, Anastasia  [Clear All Filters]
2017
Paraskevas, G. P., Kasselimis D., Kourtidou E., Constantinides V., Bougea A., Potagas C., et al. (2017).  Cerebrospinal Fluid Biomarkers as a Diagnostic Tool of the Underlying Pathology of Primary Progressive Aphasia.. J Alzheimers Dis. 55(4), 1453-1461.
Bourbouli, M., Rentzos M., Bougea A., Zouvelou V., Constantinides V. C., Zaganas I., et al. (2017).  Cerebrospinal Fluid TAR DNA-Binding Protein 43 Combined with Tau Proteins as a Candidate Biomarker for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Spectrum Disorders.. Dement Geriatr Cogn Disord. 44(3-4), 144-152.
Constantinides, V. C., Paraskevas G. P., Emmanouilidou E., Petropoulou O., Bougea A., Vekrellis K., et al. (2017).  CSF biomarkers β-amyloid, tau proteins and a-synuclein in the differential diagnosis of Parkinson-plus syndromes.. J Neurol Sci. 382, 91-95.
Bougea, A., Velonakis G., Spantideas N., Anagnostou E., Paraskevas G., Kapaki E., et al. (2017).  The first Greek case of heterozygous cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy: An atypical clinico-radiological presentation.. Neuroradiol J. 30(6), 583-585.
Bougea, A., Koros C., Stamelou M., Simitsi A., Papagiannakis N., Antonelou R., et al. (2017).  Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene.. Parkinsonism Relat Disord. 35, 82-87.
Bosco, P., Redolfi A., Bocchetta M., Ferrari C., Mega A., Galluzzi S., et al. (2017).  The impact of automated hippocampal volumetry on diagnostic confidence in patients with suspected Alzheimer's disease: A European Alzheimer's Disease Consortium study.. Alzheimers Dement. 13(9), 1013-1023.
Papadimas, G. K., Paraskevas G. P., Zambelis T., Karagiaouris C., Bourbouli M., Bougea A., et al. (2017).  The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.. Acta Myol. 36(4), 203-206.
Paraskevas, G. P., Yapijakis C., Bougea A., Constantinides V., Bourbouli M., Stamboulis E., et al. (2017).  Novel PANK2 mutation in the first Greek compound heterozygote patient with pantothenate-kinase-associated neurodegeneration.. SAGE Open Med Case Rep. 5, 2050313X17720101.

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