Mike Hutton

发表

Plasma amyloid β protein is elevated in late-onset Alzheimer disease families

S. Younkin, L. Younkin, M. Hutton, 2008, Neurology.

Familial Frontotemporal Dementia Associated with a Novel Presenilin-1 Mutation

R. Petersen, R. Ivnik, J. Hardy, 2002, Dementia and Geriatric Cognitive Disorders.

Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation

S. Lovestone, R. Dayanandan, S. Lovestone, 1999, FEBS letters.

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)

D H Geschwind, D B Calne, D. Geschwind, 2004, Neurology.

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

B. Ghetti, K. Arima, R. Uitti, 2002, Neurology.

Association between apolipoprotein E genotype and Alzheimer disease in African American subjects.

Robert C Green, David Bachman, L Adrienne Cupples, 2002, Archives of neurology.

The genetic and pathological classification of familial frontotemporal dementia.

J. Hardy, P. Lantos, M. Rossor, 2001, Archives of neurology.

Mutation in the tau exon 10 splice site region in familial frontotemporal dementia

J. Hardy, M. Rossor, A. Lees, 1999, Annals of neurology.

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes

J. Hardy, A. Goate, R. Caselli, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Identifying Genetic Factors in Parkinson Disease

D. Maraganore, Z. Wszolek, E. Foucar, 2002 .

Genetics of Parkinson's disease.

Mike Hutton, John Hardy, M. Farrer, 1997, Science.

Clinical features of frontotemporal dementia due to the intronic tau 10+16 mutation

R. Uitti, M. Hutton, Z. Wszolek, 2003, Neurology.