• Publications
  • Influence
Genetics of Parkinson's Disease: Genotype-Phenotype Correlations.
Since the first discovery of a specific genetic defect in the SNCA gene, encoding for α-synuclein, as a causative factor for Parkinson's disease 20 years ago, a multitude of other genes have beenExpand
  • 34
  • 3
Alpha-synuclein dimerization in erythrocytes of patients with genetic and non-genetic forms of Parkinson’s Disease
BACKGROUND Variations of α-synuclein levels or species have been reported in Parkinson's Disease (PD). There has been little systematic examination of erythrocytes, a rich source of α-synuclein. Expand
  • 19
  • 2
Effects of AraC treatment on motor coordination and cerebellar cytoarchitecture in the adult rat. A possible protective role of NAC.
Intact cerebellum cytoarchitecture and cellular communication are indispensable for successful motor coordination and certain forms of memory. Cytosine arabinoside (AraC), often used as anExpand
  • 26
  • 1
Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients
Reduced expression of lysosomal‐associated membrane protein 2a and heatshock‐cognate 70 proteins, involved in chaperone‐mediated autophagy and of glucocerebrosidase, is reported in PD brains. The aimExpand
  • 29
  • 1
Serotonergic pathology and disease burden in the premotor and motor phase of A53T α-synuclein parkinsonism: a cross-sectional study
BACKGROUND Because of the highly penetrant gene mutation and clinical features consistent with idiopathic Parkinson's disease, carriers of the autosomal dominant Ala53Thr (A53T; 209G→A) pointExpand
  • 23
  • 1
Environmental and tactile stimulation modulates the neonatal handling effect on adult rat spatial memory
Handling of rat pups promotes their adult cognitive performance. However, new data suggest that individual components of the handling procedure, like exposure to novelty or tactile stimulation, haveExpand
  • 18
  • 1
Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene.
INTRODUCTION The p.A53T point mutation in SNCA, the alpha-synuclein gene, has been linked to a rare dominant form of Parkinson's disease (PD). METHODS Here, we describe two apparently unrelatedExpand
  • 17
  • 1
Pure ocular anti‐musk myasthenia under no immunosuppressive treatment
A 20-year-old man presented with a 6-month history of diplopia and left eyelid ptosis. Symptoms had diurnal variation, worsened in the evening, and improved after rest. There were no symptoms orExpand
  • 13
  • 1
Neurofilament isoform alterations in the rat cerebellum following cytosine arabinoside administration.
A number of neurotoxic agents could potentially exert their action by degrading or modifying cytoskeleton components like neurofilaments (NF). Cytosine arabinoside (AraC) is an anticancer drugExpand
  • 11
  • 1
The relationship between environmental factors and different Parkinson's disease subtypes in Greece: Data analysis of the Hellenic Biobank of Parkinson's disease.
INTRODUCTION The aim of this study is to investigate the association between environmental factors (smoking, coffee, pesticide exposure) and Parkinson's disease (PD) subtypes (early-onset,Expand
  • 6
  • 1