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Efthymia Kafantari
affiliated with the university
Research project participant
,
Clinical Neurogenetics
Research support
,
MultiPark: Multidisciplinary research focused on Parkinson“s disease
Research student
,
Neurology, Lund
Email
efthymia.kafantarimed.luse
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Research output
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Dive into the research topics where Efthymia Kafantari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Weight
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Medicine & Life Sciences
Ataxia
100%
Whole Exome Sequencing
90%
Whole Genome Sequencing
88%
Tremor
81%
Genetic Testing
78%
Sweden
74%
Movement Disorders
63%
Cognitive Dysfunction
62%
Stroke
51%
Mutation
42%
Genes
38%
Idiopathic basal ganglia calcification 1
34%
Phenotype
34%
Primary Dysautonomias
27%
Cerebral Small Vessel Diseases
27%
Genetic Databases
24%
Tandem Repeat Sequences
24%
Dystonia
22%
Paraplegia
22%
Arterioles
20%
Cerebral Hemorrhage
20%
Genetic Association Studies
20%
Cerebrovascular Disorders
19%
Basal Ganglia
19%
Gait
18%
White Matter
17%
Patient Selection
16%
Virulence
16%
Vascular Endothelial Growth Factor A
16%
Autopsy
15%
Communication
14%
Arteries
14%
Genotype
13%
Technology
12%
Biopsy
11%
Skin
10%
Brain
9%