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 Angelini

Showing results (91-100 of 531) with videos related to

Pageof 54
Sort By:
Journal of Medical Genetics|May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patientsC Boito, M Fanin, G Siciliano, et al.
Minerva Medica|July 7, 1976
[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract]G Conte, C Angelini, C Locatelli, et al.
Journal of Clinical Pathology|January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanismG Cenacchi, M Fanin, L B De Giorgi, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Journal of Neurology|May 14, 1999
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophyF Martinello, A Piazza, E Pastorello, et al.
European Journal of Neurology|October 8, 2004
Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathyK Kawabe, K Goto, I Nishino, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Japanese Heart Journal|January 1, 1990
Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNAP Melacini, C Angelini, G Buja, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|April 1, 1984
[Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]P Fardin, G F Micaglio, C Angelini, et al.
Human Mutation|February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypesF Schiavon, A Rampazzo, L Merlini, et al.
Pageof 54

Showing results (91-100 of 531) with videos related to

Sort By:
Pageof 54
Journal of Medical Genetics|May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patientsC Boito, M Fanin, G Siciliano, et al.
Minerva Medica|July 7, 1976
[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract]G Conte, C Angelini, C Locatelli, et al.
Journal of Clinical Pathology|January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanismG Cenacchi, M Fanin, L B De Giorgi, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Journal of Neurology|May 14, 1999
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophyF Martinello, A Piazza, E Pastorello, et al.
European Journal of Neurology|October 8, 2004
Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathyK Kawabe, K Goto, I Nishino, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Japanese Heart Journal|January 1, 1990
Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNAP Melacini, C Angelini, G Buja, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|April 1, 1984
[Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]P Fardin, G F Micaglio, C Angelini, et al.
Human Mutation|February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypesF Schiavon, A Rampazzo, L Merlini, et al.
Pageof 54