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UnknownΤhe Greek Variant in APP Gene: The Phenotypic Spectrum of APP Mutations.
Not available
S-EPMC8622139 | biostudies-literature
UnknownTDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT.
Not available
S-EPMC3906605 | biostudies-literature
UnknownMotor and Non-motor Outcomes of Deep Brain Stimulation across the Genetic Panorama of Parkinson's Disease: A Multi-Scale Meta-Analysis.
Not available
S-EPMC11078493 | biostudies-literature
UnknownIsolated Non-Progressive Hemidystonia in a Patient Homozygous for H63D Variant of Hereditary Hemochromatosis: A Case Report and Systematic Literature Review of Movement Disorders in Hereditary Hemochromatosis.
Not available
S-EPMC12428325 | biostudies-literature
UnknownSORL1 mutation in a Greek family with Parkinson's disease and dementia.
Not available
S-EPMC8528452 | biostudies-literature
UnknownAssociation between AKT1 gene and Parkinson's disease: a protective haplotype.
Not available
S-EPMC8958471 | biostudies-literature
UnknownReal-World Open-Label Experience with Rimegepant for the Acute Treatment of Migraine Attacks: A Multicenter Pilot Study
Not available
S-EPMC11674050 | biostudies-literature
UnknownIntergenic SNPs in Obstructive Sleep Apnea Syndrome: Revealing Metabolic, Oxidative Stress and Immune-Related Pathways.
Not available
S-EPMC8534397 | biostudies-literature
UnknownThe Utilization and Impact of Dopamine Transporter Imaging in Diagnosing Movement Disorders at a Tertiary Care Hospital in Greece.
Not available
S-EPMC12024717 | biostudies-literature
UnknownAssessment of Parkinson's disease risk loci in Greece.
Not available
S-EPMC3830580 | biostudies-literature
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