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 Rodolico

Showing results (31-40 of 46) with videos related to

Pageof 5
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic lociC Rodolico, A Toscano, A Patitucci, et al.
Human Mutation|February 19, 2000
Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero geneM Muglia, A Toscano, A L Gabriele, et al.
Acta Neurologica Scandinavica|January 11, 2007
RAGE-NF-kappaB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophyV Macaione, M Aguennouz, C Rodolico, et al.
Thyroid : Official Journal of the American Thyroid Association|December 16, 1998
Myopathy as the persistently isolated symptomatology of primary autoimmune hypothyroidismC Rodolico, A Toscano, S Benvenga, et al.
Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.
Acta Neurologica Scandinavica|November 17, 2007
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathiesV Macaione, M Aguennouz, A Mazzeo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 19, 2025
NfL as a biomarker in ATTRv amyloidosis: potential and limitationsMassimo Russo, M De Luca, L Gentile, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Cell Biochemistry and Function|August 26, 2016
MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2BM Aguennouz, C Lo Giudice, N Licata, et al.
Archives of Gerontology and Geriatrics|January 1, 1996
Late-onset mitochondrial neuromyopathy: an age-related phenomenon?A Toscano, M Santoro, G Vita, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic lociC Rodolico, A Toscano, A Patitucci, et al.
Human Mutation|February 19, 2000
Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero geneM Muglia, A Toscano, A L Gabriele, et al.
Acta Neurologica Scandinavica|January 11, 2007
RAGE-NF-kappaB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophyV Macaione, M Aguennouz, C Rodolico, et al.
Thyroid : Official Journal of the American Thyroid Association|December 16, 1998
Myopathy as the persistently isolated symptomatology of primary autoimmune hypothyroidismC Rodolico, A Toscano, S Benvenga, et al.
Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.
Acta Neurologica Scandinavica|November 17, 2007
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathiesV Macaione, M Aguennouz, A Mazzeo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 19, 2025
NfL as a biomarker in ATTRv amyloidosis: potential and limitationsMassimo Russo, M De Luca, L Gentile, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Cell Biochemistry and Function|August 26, 2016
MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2BM Aguennouz, C Lo Giudice, N Licata, et al.
Archives of Gerontology and Geriatrics|January 1, 1996
Late-onset mitochondrial neuromyopathy: an age-related phenomenon?A Toscano, M Santoro, G Vita, et al.
Pageof 5