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N C Fox

Showing results (91-100 of 115) with videos related to

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International Journal of Geriatric Psychiatry|January 20, 2010
Memory complaints and increased rates of brain atrophy: risk factors for mild cognitive impairment and Alzheimer's diseaseH A Archer, J Kennedy, J Barnes, et al.
AJNR. American Journal of Neuroradiology|February 13, 2010
Onset and progression of pathologic atrophy in Huntington disease: a longitudinal MR imaging studyN Z Hobbs, J Barnes, C Frost, et al.
Neurology|April 24, 2002
Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutationJ C Janssen, E K Warrington, H R Morris, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2002
Progressive ventricular enlargement in patients with clinically isolated syndromes is associated with the early development of multiple sclerosisC M Dalton, P A Brex, R Jenkins, et al.
Neurology|February 26, 2000
Progressive cerebral atrophy in MS: a serial study using registered, volumetric MRIN C Fox, R Jenkins, S M Leary, et al.
Neuroimage|December 19, 2006
Improved reliability of hippocampal atrophy rate measurement in mild cognitive impairment using fluid registrationL A van de Pol, J Barnes, R I Scahill, et al.
Brain : a Journal of Neurology|April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological studyJ C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology|May 20, 2005
Brain biopsy in dementiaJ D Warren, J M Schott, N C Fox, et al.
Brain : a Journal of Neurology|March 1, 1997
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 factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.
Pageof 12

Showing results (91-100 of 115) with videos related to

Sort By:
Pageof 12
International Journal of Geriatric Psychiatry|January 20, 2010
Memory complaints and increased rates of brain atrophy: risk factors for mild cognitive impairment and Alzheimer's diseaseH A Archer, J Kennedy, J Barnes, et al.
AJNR. American Journal of Neuroradiology|February 13, 2010
Onset and progression of pathologic atrophy in Huntington disease: a longitudinal MR imaging studyN Z Hobbs, J Barnes, C Frost, et al.
Neurology|April 24, 2002
Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutationJ C Janssen, E K Warrington, H R Morris, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2002
Progressive ventricular enlargement in patients with clinically isolated syndromes is associated with the early development of multiple sclerosisC M Dalton, P A Brex, R Jenkins, et al.
Neurology|February 26, 2000
Progressive cerebral atrophy in MS: a serial study using registered, volumetric MRIN C Fox, R Jenkins, S M Leary, et al.
Neuroimage|December 19, 2006
Improved reliability of hippocampal atrophy rate measurement in mild cognitive impairment using fluid registrationL A van de Pol, J Barnes, R I Scahill, et al.
Brain : a Journal of Neurology|April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological studyJ C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology|May 20, 2005
Brain biopsy in dementiaJ D Warren, J M Schott, N C Fox, et al.
Brain : a Journal of Neurology|March 1, 1997
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 factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.
Pageof 12