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

B Nacmias

Showing results (11-20 of 61) with videos related to

Pageof 7
Sort By:
Annals of Neurology|July 1, 1995
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's diseaseS Sorbi, B Nacmias, P Forleo, et al.
Neuroscience Letters|May 16, 1997
Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob diseaseM Salvatore, A C Seeber, B Nacmias, et al.
Neuroscience Letters|January 7, 2000
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosaB Nacmias, V Ricca, A Tedde, et al.
Lancet (London, England)|June 23, 1998
5-HT2A promoter polymorphism in anorexia nervosaS Sorbi, B Nacmias, A Tedde, et al.
Journal of Neurology|September 25, 2001
Clinical and genetic analysis of an Italian family with Machado-Joseph diseaseP Forleo, E Cellini, L Parnetti, et al.
Mechanisms of Ageing and Development|October 9, 2001
Genetic risk factors in familial Alzheimer's diseaseS Sorbi, P Forleo, A Tedde, et al.
Neuroscience Letters|November 17, 2001
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's diseaseT Brunelli, S Bagnoli, B Giusti, et al.
Neurology|November 30, 2000
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onsetA Tedde, P Forleo, B Nacmias, et al.
Nature Medicine|September 1, 1995
ApoE as a prognostic factor for post-traumatic comaS Sorbi, B Nacmias, S Piacentini, et al.
Neuroscience Letters|January 31, 1997
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's diseaseS Sorbi, B Nacmias, A Tedde, et al.
Pageof 7

Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
Annals of Neurology|July 1, 1995
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's diseaseS Sorbi, B Nacmias, P Forleo, et al.
Neuroscience Letters|May 16, 1997
Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob diseaseM Salvatore, A C Seeber, B Nacmias, et al.
Neuroscience Letters|January 7, 2000
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosaB Nacmias, V Ricca, A Tedde, et al.
Lancet (London, England)|June 23, 1998
5-HT2A promoter polymorphism in anorexia nervosaS Sorbi, B Nacmias, A Tedde, et al.
Journal of Neurology|September 25, 2001
Clinical and genetic analysis of an Italian family with Machado-Joseph diseaseP Forleo, E Cellini, L Parnetti, et al.
Mechanisms of Ageing and Development|October 9, 2001
Genetic risk factors in familial Alzheimer's diseaseS Sorbi, P Forleo, A Tedde, et al.
Neuroscience Letters|November 17, 2001
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's diseaseT Brunelli, S Bagnoli, B Giusti, et al.
Neurology|November 30, 2000
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onsetA Tedde, P Forleo, B Nacmias, et al.
Nature Medicine|September 1, 1995
ApoE as a prognostic factor for post-traumatic comaS Sorbi, B Nacmias, S Piacentini, et al.
Neuroscience Letters|January 31, 1997
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's diseaseS Sorbi, B Nacmias, A Tedde, et al.
Pageof 7