A. Kennedy

发表

Presymptomatic hippocampal atrophy in Alzheimer's disease. A longitudinal MRI study.

Nick C Fox, P. A. Freeborough, J. Stevens, 1996, Brain : a journal of neurology.

Neuropsychological profiles of familial Alzheimer's disease associated with mutations in the presenilin 1 and amyloid precursor protein genes

M. Rossor, E. Warrington, A. Kennedy, 2001, Journal of Neurology.

Impairment of Neocortical Metabolism Predicts Progression in Alzheimer’s Disease

F. Fazio, R. Mielke, D. Perani, 1999, Dementia and Geriatric Cognitive Disorders.

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

M. Adams, N. Fox, J. Venter, 1995, Nature Genetics.

Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology.

M. Rossor, A. Kennedy, H. Houlden, 1993, American journal of medical genetics.

APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE

J. Hardy, B. Winblad, M. Rossor, 1993 .

PRESYMPTOMATIC DEFICITS IN INDIVIDUALS AT RISK OF FAMILIAL ALZHEIMERS-DISEASE - A POSITRON EMISSION TOMOGRAPHY STUDY

R. Frackowiak, M. Rossor, A. Kennedy, 1994 .

Familial and sporadic Alzheimer's disease

M. Rossor, A. Kennedy, Hodges, 2001 .

Management of dementia.

M. Rossor, A. Kennedy, 1993, The Practitioner.

Alzheimer's Disease Families with Amyloid Precursor Protein Mutations a

P. Lantos, A. Kennedy, R. Frackowiak, 1993, Annals of the New York Academy of Sciences.

Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.

Nick C Fox, J. Hardy, P. Lantos, 1997, Brain : a journal of neurology.

Genetics of Alzheimer's disease.

M. Farrall, M. Rossor, A. Goate, 1990 .

Clinical and Neuroimaging Features of Familial Alzheimer's Disease a

R. Frackowiak, A. Kennedy, M. Rossor, 1996, Annals of the New York Academy of Sciences.

Familial Alzheimer's disease. A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine-->glycine).

R. Frackowiak, J. Hardy, E. Warrington, 1993, Brain : a journal of neurology.

Chromosome 14 linked familial Alzheimer's disease. A clinico-pathological study of a single pedigree.

R. Frackowiak, D. Neary, J. Stevens, 1995, Brain : a journal of neurology.

The earliest cognitive change in a person with familial Alzheimer's disease: presymptomatic neuropsychological features in a pedigree with familial Alzheimer's disease confirmed at necropsy.

M. Rossor, E. Warrington, A. Kennedy, 1994, Journal of neurology, neurosurgery, and psychiatry.

A NEUROIMAGING STUDY OF INDIVIDUALS WITH APP MUTATIONS

Nick C. Fox, Martin N. Rossor, Nick C Fox, 1994 .

disease confirmed at necropsy . in a pedigree with familial Alzheimer ' s presymptomatic neuropsychological features with familial Alzheimer ' s disease : The earliest cognitive change in a person

M. Rossor, E. Warrington, A. Kennedy, 2022 .