Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 15 results:
Author Title Type [ Year] Filters: Author is Kapaki, Elisabeth [Clear All Filters]
Association of Cerebral Amyloid-β Aggregation With Cognitive Functioning in Persons Without Dementia..
JAMA Psychiatry. 75(1), 84-95.
(2018). The different faces of the p. A53T alpha-synuclein mutation: A screening of Greek patients with parkinsonism and/or dementia..
Neurosci Lett. 672, 136-139.
(2018). Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort..
Amyotroph Lateral Scler Frontotemporal Degener. 19(1-2), 152-154.
(2018). Simple linear brainstem MRI measurements in the differential diagnosis of progressive supranuclear palsy from the parkinsonian variant of multiple system atrophy..
Neurol Sci. 39(2), 359-364.
(2018). An unusual phenocopy of the HANAC syndrome without genetic involvement of COL4A1/COL4A2..
Acta Neurol Belg. 118(1), 135-136.
(2018). Update on Vascular Cognitive Impairment Associated with Subcortical Small-Vessel Disease..
J Alzheimers Dis. 62(3), 1417-1441.
(2018). Cerebrospinal Fluid Biomarkers as a Diagnostic Tool of the Underlying Pathology of Primary Progressive Aphasia..
J Alzheimers Dis. 55(4), 1453-1461.
(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.
(2017). CSF biomarkers β-amyloid, tau proteins and a-synuclein in the differential diagnosis of Parkinson-plus syndromes..
J Neurol Sci. 382, 91-95.
(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.
(2017). Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene..
Parkinsonism Relat Disord. 35, 82-87.
(2017). The multifaceted clinical presentation of VCP-proteinopathy in a Greek family..
Acta Myol. 36(4), 203-206.
(2017). Novel PANK2 mutation in the first Greek compound heterozygote patient with pantothenate-kinase-associated neurodegeneration..
SAGE Open Med Case Rep. 5, 2050313X17720101.
(2017). Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysis..
JAMA. 313(19), 1924-38.
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