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Gender effects on clinical features in LRRK2 G2385R carriers and non-carriers in Parkinson’s disease
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Gender-specific pattern of sensori-motor network connectivity in early untreated Parkinson’s disease patients
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Generalized chorea in a patient with isolated leukocytosis and JAK2V617F mutation: A case report
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Generalized choreoathetoid-like movements in primary Sjögren syndrome
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Generalized dystonia and chorea with family history: Clinical case
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Generation and in-depth characterization of induced pluripotent stem cell (iPSC) lines from 10 affected and unaffected carriers of THAP1 mutations
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Genetic analysis of Wilson’s disease in Taiwan
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Genetic defects causing complex movement disorders and basal ganglia degeneration in childhood
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Genetic Markers of Essential Tremor in Restless Legs Syndrome/Willis-Ekbom Disease in Southern Chinese Population
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Genetic variations of SNCA and striatal dopaminergic dysfunction in patients with Parkinson’s disease
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