Are mitochondria critical in the pathogenesis of Alzheimer's disease?

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Amyloid ?? peptide induces cytochrome c release from isolated mitochondria

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Evidence for Physiological Down-regulation of Brain Oxidative Phosphorylation in Alzheimer's Disease

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Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease

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Oxidative phosphorylation defects and Alzheimer's disease

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Association of the mitochondrial tRNA^A4336G mutation with Alzheimer's and Parkinson's diseases

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Leigh Syndrome with Cytochrome-c Oxidase Deficiency and a Single T Insertion nt 5537 in the Mitochondrial tRNA^TrpGene

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Aberrant Splicing of Exon 6 in the Pyruvate Denydrogenase-Elα mRNA Linked to a Silent Mutation in a Large Family with Leigh's Encephalomyelopathy

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Isolation, Characterization and Structural Organization of the Gene and Pseudogene for the Dihydrolipoamide Succinyltransferase Component of the Human 2‐Oxoglutarate Dehydrogenase Complex

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Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit

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MtDNA Mutations in Maternally Inherited Diabetes: Presence of the 3397 ND1 Mutation Previously Associated with Alzheimer's and Parkinson's Disease

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Alzheimer's Disease

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A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis

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