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Nature Reviews. Neuroscience|June 21, 2012
Use of next-generation sequencing and other whole-genome strategies to dissect neurological diseaseJose Bras, Rita Guerreiro, John HardyMethodsx|August 3, 2023
Development of bespoke hardware and software to enable testing of a novel method of managing the charge and discharge of series-connected battery packsJohn Hardy, John Steggall, Peter HardyNeuron|May 12, 2023
A dynamical systems approach for multiscale synthesis of Alzheimer's pathogenesisJennifer Rollo, John Crawford, John HardyBiochemical Society Transactions|November 14, 2009
Whole genome expression as a quantitative traitJohn Hardy, Danyah Trabzuni, Mina RytenCurrent Opinion in Neurology|July 3, 2013
The pallidopyramidal syndromes: nosology, aetiology and pathogenesisEleanna Kara, John Hardy, Henry HouldenJournal of Alzheimer'S Disease : JAD|June 10, 2011
APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysisTerhi Peuralinna, Maarit Tanskanen, Mira Mäkelä, et al.American Journal of Human Genetics|April 21, 2009
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseAndrew J Duncan, Maria Bitner-Glindzicz, Brigitte Meunier, et al.Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.Annals of Neurology|September 1, 2005
Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic strokeJames F Meschia, Thomas G Brott, Robert D Brown, et al.Pageof 94