The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease

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α-Synuclein Locus Triplication Causes Parkinson's Disease

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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

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Mitochondrial diseases in man and mouse

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The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia

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Mitochondrial form and function

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Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

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Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

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High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

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ABAD Directly Links Aß to Mitochondrial Toxicity in Alzheimer's Disease

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Impaired Balance of Mitochondrial Fission and Fusion in Alzheimer's Disease

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Mitochondrial Import and Accumulation of α-Synuclein Impair Complex I in Human Dopaminergic Neuronal Cultures and Parkinson Disease Brain

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Direct Membrane Association Drives Mitochondrial Fission by the Parkinson Disease-associated Protein α-Synuclein

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