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

P Giunti

Showing results (11-20 of 52) with videos related to

Pageof 6
Sort By:
Behavioural Neurology|June 1, 2017
Erratum: Preliminary Characterisation of Cognition and Social Cognition in Spinocerebellar Ataxia Types 2, 1, and 7N Sokolovsky, A Cook, H Hunt, et al.
Behavioural Neurology|August 18, 2010
A preliminary characterisation of cognition and social cognition in spinocerebellar ataxia types 2, 1, and 7N Sokolovsky, A Cook, H Hunt, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Hemorrheology and neurovascular syndromes of the extremities]G Sergio, F Artale, A Francisci, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Influence of age factors on the rheological properties of blood in healthy subjects and those with vascular disease]F Artale, G Sergio, P Giunti, et al.
Current Medical Research and Opinion|January 1, 1986
Haemorrheological improvement by pentoxifylline in patients with peripheral arterial occlusive diseaseM A Perego, G Sergio, F Artale, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Hemorrheological factors in the developmental stages of peripheral arterial occlusive diseases]F Artale, G Sergio, L Cramarossa, et al.
Minerva Cardioangiologica|July 1, 1981
[Regional study of the principal hemorheological factors in peripheral obstructive arteriopathy. I]F Artale, G Sergio, M Espureo, et al.
Italian Journal of Neurological Sciences|January 1, 1993
Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onsetM Spadaro, P Giunti, G B Colazza, et al.
Nature Genetics|March 4, 2000
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxiaP F Worth, H Houlden, P Giunti, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Behavioural Neurology|June 1, 2017
Erratum: Preliminary Characterisation of Cognition and Social Cognition in Spinocerebellar Ataxia Types 2, 1, and 7N Sokolovsky, A Cook, H Hunt, et al.
Behavioural Neurology|August 18, 2010
A preliminary characterisation of cognition and social cognition in spinocerebellar ataxia types 2, 1, and 7N Sokolovsky, A Cook, H Hunt, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Hemorrheology and neurovascular syndromes of the extremities]G Sergio, F Artale, A Francisci, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Influence of age factors on the rheological properties of blood in healthy subjects and those with vascular disease]F Artale, G Sergio, P Giunti, et al.
Current Medical Research and Opinion|January 1, 1986
Haemorrheological improvement by pentoxifylline in patients with peripheral arterial occlusive diseaseM A Perego, G Sergio, F Artale, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1983
[Hemorrheological factors in the developmental stages of peripheral arterial occlusive diseases]F Artale, G Sergio, L Cramarossa, et al.
Minerva Cardioangiologica|July 1, 1981
[Regional study of the principal hemorheological factors in peripheral obstructive arteriopathy. I]F Artale, G Sergio, M Espureo, et al.
Italian Journal of Neurological Sciences|January 1, 1993
Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onsetM Spadaro, P Giunti, G B Colazza, et al.
Nature Genetics|March 4, 2000
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxiaP F Worth, H Houlden, P Giunti, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Pageof 6