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15.097 articles found

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Genetic Variants Associated With Neurodegenerative Disorders in Patients With Amyotrophic Lateral Sclerosis and Phenotypic Variability.

Grassano M, Koumantakis E, Palumbo FF, Brunetti M, De Marco G, Merulla I, Paolantonio C, Iazzolino B, Testa M, Manera U, Canosa A, Vasta R, Fuda G, Salamone P, Marchese G, Casale F, Gallone S, Mora G, Moglia C, Calvo A, Chiò A.

Neurology · 2025-09-25

DOI: 10.1212/wnl.0000000000214180PMID: 40997283

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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VMAT2 dysfunction impairs vesicular dopamine uptake, driving its oxidation and α-synuclein pathology in DJ-1-linked Parkinson’s disease neurons

Heger LM, Gubinelli F, Huber A, Cardona-Alberich A, Rovere M, Matti U, Müller SA, Nagaraja SR, Jaschkowitz L, Schifferer M, Wurst W, Lichtenthaler SF, Behrends C, Sambandan S, Burbulla LF.

· 2025-09-22

DOI: 10.1101/2025.09.22.677565

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access

Secondary nucleation of α-Synuclein drives Mitochondria dysfunctions and Lewy body formation in Parkinson’s Disease

De S, Prescott E, Wei J, Garland E, Urbanek A, Capriglia F, Molenkamp W, Rhodes D, Heywood L, Schwartzentruber A, Stephen E, Hughes R, Bandmann O, Collins M, Linse S, Abelein A, Johansson J, Vendruscolo M, Highley J, Knowles T, Mortiboys H.

· 2025-09-22

DOI: 10.21203/rs.3.rs-7657706/v1

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

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