Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C BRUNI

Showing results (71-80 of 152) with videos related to

Pageof 16
Sort By:
Archives of Neurology|November 16, 2005
Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementiaEnzo Emanuele, Angela D'Angelo, Carmine Tomaino, et al.
Journal of Alzheimer'S Disease : JAD|March 1, 2016
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 CarriersAlberto Montesanto, Paolina Crocco, Maria Anfossi, et al.
Revue Neurologique|January 1, 1985
[Alzheimer's presenile dementia transmitted in an extended kindred]J F Foncin, D Salmon, V Supino-Viterbo, et al.
Journal of Neurology|February 12, 2015
Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairmentRoberta Perri, Marco Monaco, Lucia Fadda, et al.
Neuroscience Letters|March 24, 2004
Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's diseaseEnzo Emanuele, Emmanouil Peros, Carmine Tomaino, et al.
Annals of Human Genetics|May 29, 2008
Cognitive functioning and survival in the elderly: the SSADH C538T polymorphismF De Rango, O Leone, S Dato, et al.
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Minerva Chirurgica|April 15, 1991
[The management of head trauma in a general surgery department. a contribution to an epidemiological analysis]G Grasso, A Lenzi, G C Bruni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17Elena Salvatore, Andrea Varrone, Valeria Sansone, et al.
Acta Endocrinologica|March 1, 1982
A case of ectopic ACTH syndrome: diagnostic difficulties caused by intermittent hormone secretionM O Thorner, W H Martin, G E Ragan, et al.
Pageof 16

Showing results (71-80 of 152) with videos related to

Sort By:
Pageof 16
Archives of Neurology|November 16, 2005
Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementiaEnzo Emanuele, Angela D'Angelo, Carmine Tomaino, et al.
Journal of Alzheimer'S Disease : JAD|March 1, 2016
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 CarriersAlberto Montesanto, Paolina Crocco, Maria Anfossi, et al.
Revue Neurologique|January 1, 1985
[Alzheimer's presenile dementia transmitted in an extended kindred]J F Foncin, D Salmon, V Supino-Viterbo, et al.
Journal of Neurology|February 12, 2015
Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairmentRoberta Perri, Marco Monaco, Lucia Fadda, et al.
Neuroscience Letters|March 24, 2004
Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's diseaseEnzo Emanuele, Emmanouil Peros, Carmine Tomaino, et al.
Annals of Human Genetics|May 29, 2008
Cognitive functioning and survival in the elderly: the SSADH C538T polymorphismF De Rango, O Leone, S Dato, et al.
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Minerva Chirurgica|April 15, 1991
[The management of head trauma in a general surgery department. a contribution to an epidemiological analysis]G Grasso, A Lenzi, G C Bruni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17Elena Salvatore, Andrea Varrone, Valeria Sansone, et al.
Acta Endocrinologica|March 1, 1982
A case of ectopic ACTH syndrome: diagnostic difficulties caused by intermittent hormone secretionM O Thorner, W H Martin, G E Ragan, et al.
Pageof 16