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

M Mochi

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Cephalalgia : an International Journal of Headache|February 1, 1994
Abnormal platelet mitochondrial function in patients affected by migraine with and without auraS Sangiorgi, M Mochi, R Riva, et al.
Journal of Neurology|September 25, 2001
Dopaminergic pathways involvement in Kennedy's disease: neurophysiological andD Soragna, C Messa, M Mochi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2003
The genetics of chronic headachesP Montagna, S Cevoli, N Marzocchi, et al.
European Journal of Neurology|August 26, 2006
A genetic association study of dopamine metabolism-related genes and chronic headache with drug abuseS Cevoli, M Mochi, C Scapoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2002
Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian familyS Cevoli, G Pierangeli, L Monari, et al.
Cephalalgia : an International Journal of Headache|December 1, 1993
Testing models for genetic determination in migraineM Mochi, S Sangiorgi, P Cortelli, et al.
Archives of Gerontology and Geriatrics. Supplement|June 30, 2001
Prevalence of depression and cognitive deficit in a geriatric populationA Silverstri, G Visconti, M Fini, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Brain & Development|October 24, 2000
Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matterA Parmeggiani, A Posar, L B De Giorgi, et al.
Italian Journal of Neurological Sciences|June 1, 1997
Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsyM Mochi, F Provini, G Plazzi, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Cephalalgia : an International Journal of Headache|February 1, 1994
Abnormal platelet mitochondrial function in patients affected by migraine with and without auraS Sangiorgi, M Mochi, R Riva, et al.
Journal of Neurology|September 25, 2001
Dopaminergic pathways involvement in Kennedy's disease: neurophysiological andD Soragna, C Messa, M Mochi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2003
The genetics of chronic headachesP Montagna, S Cevoli, N Marzocchi, et al.
European Journal of Neurology|August 26, 2006
A genetic association study of dopamine metabolism-related genes and chronic headache with drug abuseS Cevoli, M Mochi, C Scapoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2002
Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian familyS Cevoli, G Pierangeli, L Monari, et al.
Cephalalgia : an International Journal of Headache|December 1, 1993
Testing models for genetic determination in migraineM Mochi, S Sangiorgi, P Cortelli, et al.
Archives of Gerontology and Geriatrics. Supplement|June 30, 2001
Prevalence of depression and cognitive deficit in a geriatric populationA Silverstri, G Visconti, M Fini, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Brain & Development|October 24, 2000
Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matterA Parmeggiani, A Posar, L B De Giorgi, et al.
Italian Journal of Neurological Sciences|June 1, 1997
Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsyM Mochi, F Provini, G Plazzi, et al.
Pageof 3