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D Campion

Showing results (51-60 of 146) with videos related to

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Molecular Psychiatry|March 30, 2016
Alzheimer disease: modeling an Aβ-centered biological networkD Campion, C Pottier, G Nicolas, et al.
The New England Journal of Medicine|February 1, 1979
Phosphorylation of red-cell membrane proteins in Duchenne muscular dystrophyR S Falk, D Campion, D Guthrie, et al.
International Journal of Health Care Quality Assurance Incorporating Leadership in Health Services|December 8, 1997
The outpatient experience: results of a patient feedback surveyK McKinnon, P D Crofts, R Edwards, et al.
Human Mutation|June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's diseaseG Raux, R Gantier, C Martin, et al.
Neuroscience Letters|April 8, 2000
The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 betaR Gantier, D Gilbert, C Dumanchin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 20, 2007
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhageA Rovelet-Lecrux, T Frebourg, H Tuominen, et al.
Revue Neurologique|July 14, 2009
[Insanity in the young: diagnostic course]D Hannequin, L Guyant-Maréchal, I Le Ber, et al.
Computer Methods in Biomechanics and Biomedical Engineering|November 2, 2017
Finite element model of a below-knee amputation: a feasibility studyD Campion, N Dakhil, M Llari, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 14, 1998
Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNAF Salomon-Nguyen, M Le Coniat-Busson, R Heilig, et al.
Journal of Medical Genetics|February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's diseaseM L Jacquemont, D Campion, V Hahn, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Molecular Psychiatry|March 30, 2016
Alzheimer disease: modeling an Aβ-centered biological networkD Campion, C Pottier, G Nicolas, et al.
The New England Journal of Medicine|February 1, 1979
Phosphorylation of red-cell membrane proteins in Duchenne muscular dystrophyR S Falk, D Campion, D Guthrie, et al.
International Journal of Health Care Quality Assurance Incorporating Leadership in Health Services|December 8, 1997
The outpatient experience: results of a patient feedback surveyK McKinnon, P D Crofts, R Edwards, et al.
Human Mutation|June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's diseaseG Raux, R Gantier, C Martin, et al.
Neuroscience Letters|April 8, 2000
The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 betaR Gantier, D Gilbert, C Dumanchin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 20, 2007
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhageA Rovelet-Lecrux, T Frebourg, H Tuominen, et al.
Revue Neurologique|July 14, 2009
[Insanity in the young: diagnostic course]D Hannequin, L Guyant-Maréchal, I Le Ber, et al.
Computer Methods in Biomechanics and Biomedical Engineering|November 2, 2017
Finite element model of a below-knee amputation: a feasibility studyD Campion, N Dakhil, M Llari, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 14, 1998
Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNAF Salomon-Nguyen, M Le Coniat-Busson, R Heilig, et al.
Journal of Medical Genetics|February 12, 2002
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's diseaseM L Jacquemont, D Campion, V Hahn, et al.
Pageof 15