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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  • Κοινότητες & Συλλογές
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Motor and Nonmotor Features of Carriers of the p.A53T Alpha-Synuclein Mutation: A Longitudinal Study

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Συγγραφέας
Papadimitriou D., Antonelou R., Miligkos M., Maniati M., Papagiannakis N., Bostantjopoulou S., Leonardos A., Koros C., Simitsi A., Papageorgiou S.G., Kapaki E., Alcalay R.N., Papadimitriou A., Athanassiadou A., Stamelou M., Stefanis L.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1002/mds.26615
Λέξη-κλειδί
alpha synuclein
alpha synuclein
SNCA protein, human
adult
age distribution
aged
Article
autonomic dysfunction
clinical article
clinical assessment
clinical feature
cohort analysis
controlled study
correlational study
dementia
depression
disease duration
female
follow up
gene mutation
genetic risk
heterozygote
human
longitudinal study
male
mental deterioration
onset age
parasomnia
Parkinson disease
penetrance
phenotypic variation
priority journal
prospective study
rating scale
sex difference
sleep disorder
smelling disorder
Unified Parkinson Disease Rating Scale
very elderly
autonomic neuropathy
complication
dementia
genetics
heterozygote
middle aged
mutation
Parkinson disease
pathophysiology
penetrance
psychosis
smelling disorder
Adult
Aged
alpha-Synuclein
Autonomic Nervous System Diseases
Dementia
Female
Heterozygote
Humans
Longitudinal Studies
Male
Middle Aged
Mutation
Olfaction Disorders
Parkinson Disease
Penetrance
Psychotic Disorders
John Wiley and Sons Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: G209A SNCA mutation carriers represent an important group of genetic PD. We describe motor and nonmotor features of G209A SNCA mutation carriers. Methods: Longitudinal clinical assessments over 2 years were collected in 22 symptomatic and 8 asymptomatic G209A SNCA mutation carriers. Motor and nonmotor rating scales were administered. Correlations were performed between clinical variables and disease duration or age. Penetrance was calculated using Kaplan-Meier survival curves. Results: Asymptomatic carriers did not manifest clear premotor symptoms, but symptomatic carriers often reported that olfactory dysfunction and rapid eye movement sleep behavior disorder preceded motor symptoms. Prominent motor decline and deterioration of autonomic and cognitive function occurred at follow-up; such nonmotor features correlated with disease duration, but not age. Disease penetrance was estimated at around 90%. Conclusions: This study may help to inform clinical trials and provide the basis for studies of disease modifiers in genetic synucleinopathy cohorts. © 2016 International Parkinson and Movement Disorder Society. © 2016 International Parkinson and Movement Disorder Society
URI
http://hdl.handle.net/11615/77574
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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