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Cell Reports|June 11, 2013
NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological diseaseRobert D S Pitceathly, Shamima Rahman, Yehani Wedatilake, et al.
BMC Neurology|January 28, 2025
Number of children and dementia risk: a causal mediation analysis using data from the HUNT study linked with national registries in NorwayTeferi Mekonnen, Vegard Skirbekk, Ekaterina Zotcheva, et al.
Brain : a Journal of Neurology|September 9, 2016
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypesEmma S Reid, Apostolos Papandreou, Suzanne Drury, et al.
Orphanet Journal of Rare Diseases|July 9, 2013
SURF1 deficiency: a multi-centre natural history studyYehani Wedatilake, Ruth M Brown, Robert McFarland, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 24, 2024
Genetic associations with psychosis and affective disturbance in Alzheimer's diseaseInga Margret Antonsdottir, Byron Creese, Lambertus Klei, et al.
Annals of Neurology|December 6, 2017
Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 casesRoeltje R Maas, Katarzyna Iwanicka-Pronicka, Sema Kalkan Ucar, et al.
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