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

Marina Fanin

Showing results (31-40 of 56) with videos related to

Pageof 6
Sort By:
Human Mutation|December 8, 2004
Molecular and muscle pathology in a series of caveolinopathy patientsLuigi Fulizio, Anna Chiara Nascimbeni, Marina Fanin, et al.
Neuropathology and Applied Neurobiology|July 22, 2014
Familial polyglucosan body myopathy with unusual phenotypeMarina Fanin, Anna Chiara Nascimbeni, Marco Savarese, et al.
Neurological Research|September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiencyAngelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
BMC Medicine|April 9, 2009
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophyCaterina Millino, Marina Fanin, Andrea Vettori, et al.
The American Journal of Cardiology|November 15, 2011
Sudden death associated with danon disease in womenDaniela Miani, Matthew Taylor, Luisa Mestroni, et al.
Muscle & Nerve|December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1FMarina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 28, 2009
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)Sergio Salvatori, Sandra Furlan, Marina Fanin, et al.
Ultrastructural Pathology|June 24, 2010
The role of ultrastructural examination in storage diseasesValentina Papa, Lucia Tarantino, Paola Preda, et al.
Journal of Neurology|November 20, 2010
Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodiesGiovanna Cenacchi, Valentina Papa, Papa Valentina, et al.
Scientific Reports|September 2, 2016
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathiesLuca Bello, Paola Campadello, Andrea Barp, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Human Mutation|December 8, 2004
Molecular and muscle pathology in a series of caveolinopathy patientsLuigi Fulizio, Anna Chiara Nascimbeni, Marina Fanin, et al.
Neuropathology and Applied Neurobiology|July 22, 2014
Familial polyglucosan body myopathy with unusual phenotypeMarina Fanin, Anna Chiara Nascimbeni, Marco Savarese, et al.
Neurological Research|September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiencyAngelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
BMC Medicine|April 9, 2009
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophyCaterina Millino, Marina Fanin, Andrea Vettori, et al.
The American Journal of Cardiology|November 15, 2011
Sudden death associated with danon disease in womenDaniela Miani, Matthew Taylor, Luisa Mestroni, et al.
Muscle & Nerve|December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1FMarina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 28, 2009
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)Sergio Salvatori, Sandra Furlan, Marina Fanin, et al.
Ultrastructural Pathology|June 24, 2010
The role of ultrastructural examination in storage diseasesValentina Papa, Lucia Tarantino, Paola Preda, et al.
Journal of Neurology|November 20, 2010
Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodiesGiovanna Cenacchi, Valentina Papa, Papa Valentina, et al.
Scientific Reports|September 2, 2016
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathiesLuca Bello, Paola Campadello, Andrea Barp, et al.
Pageof 6