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L Cipolotti

Showing results (61-70 of 68) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2005
Mapping the onset and progression of atrophy in familial frontotemporal lobar degenerationJ C Janssen, J M Schott, L Cipolotti, et al.
Journal of the Neurological Sciences|March 31, 2004
Clinical-anatomical correlation in a selective phonemic speech production impairmentA J Larner, G Robinson, L D Kartsounis, et al.
Annals of Neurology|April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's diseaseD Chan, N C Fox, R I Scahill, 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|October 20, 2020
MRI-visible perivascular spaces as an imaging biomarker in Fabry diseaseD Lyndon, I Davagnanam, D Wilson, 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.
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.
Archives of Neurology|June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutationJ C Janssen, P L Lantos, N C Fox, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2005
Mapping the onset and progression of atrophy in familial frontotemporal lobar degenerationJ C Janssen, J M Schott, L Cipolotti, et al.
Journal of the Neurological Sciences|March 31, 2004
Clinical-anatomical correlation in a selective phonemic speech production impairmentA J Larner, G Robinson, L D Kartsounis, et al.
Annals of Neurology|April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's diseaseD Chan, N C Fox, R I Scahill, 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|October 20, 2020
MRI-visible perivascular spaces as an imaging biomarker in Fabry diseaseD Lyndon, I Davagnanam, D Wilson, 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.
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.
Archives of Neurology|June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutationJ C Janssen, P L Lantos, N C Fox, et al.
Pageof 7