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

S Messina

Showing results (81-90 of 138) with videos related to

Pageof 14
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 30, 2025
Long term clinical follow-up and natural history in a cohort of Italian patients with GNE myopathy: the experience of a single centreAlessia Pugliese, M Sframeli, P D'Ambrosio, et al.
In Vivo (Athens, Greece)|May 18, 2011
The sentinel node biopsy in patients with thick melanoma: outcome analysis from a single-institution databaseP Covarelli, M C Vedovati, C Becattini, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|January 17, 2022
The use of OCT in good visual acuity MOGAD and AQP4-NMOSD patients; with and without optic neuritisA Roca-Fernández, V Camera, G Loncarevic-Whitaker, et al.
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.
European Journal of Biochemistry|February 15, 2000
Diverting a protein from its cellular location by intracellular antibodies. The case of p21RasM Lener, I R Horn, A Cardinale, et al.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 30, 2007
Predictive factors for the development of scoliosis in Duchenne muscular dystrophyM Kinali, M Main, J Eliahoo, et al.
European Journal of Neurology|March 13, 2014
Restless legs syndrome and multiple sclerosis: a population based case-control study in Catania, SicilyE Bruno, A Nicoletti, S Messina, et al.
Oncogene|October 18, 2006
The p85 regulatory subunit of PI3K mediates TSH-cAMP-PKA growth and survival signalsG De Gregorio, A Coppa, C Cosentino, et al.
British Journal of Diseases of the Chest|October 1, 1983
Small-cell lung carcinoma: survival after combination chemotherapy, radiotherapy or symptomatic treatmentM L Slevin, V J Harvey, B A Ponder, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 30, 2025
Long term clinical follow-up and natural history in a cohort of Italian patients with GNE myopathy: the experience of a single centreAlessia Pugliese, M Sframeli, P D'Ambrosio, et al.
In Vivo (Athens, Greece)|May 18, 2011
The sentinel node biopsy in patients with thick melanoma: outcome analysis from a single-institution databaseP Covarelli, M C Vedovati, C Becattini, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|January 17, 2022
The use of OCT in good visual acuity MOGAD and AQP4-NMOSD patients; with and without optic neuritisA Roca-Fernández, V Camera, G Loncarevic-Whitaker, et al.
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.
European Journal of Biochemistry|February 15, 2000
Diverting a protein from its cellular location by intracellular antibodies. The case of p21RasM Lener, I R Horn, A Cardinale, et al.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 30, 2007
Predictive factors for the development of scoliosis in Duchenne muscular dystrophyM Kinali, M Main, J Eliahoo, et al.
European Journal of Neurology|March 13, 2014
Restless legs syndrome and multiple sclerosis: a population based case-control study in Catania, SicilyE Bruno, A Nicoletti, S Messina, et al.
Oncogene|October 18, 2006
The p85 regulatory subunit of PI3K mediates TSH-cAMP-PKA growth and survival signalsG De Gregorio, A Coppa, C Cosentino, et al.
British Journal of Diseases of the Chest|October 1, 1983
Small-cell lung carcinoma: survival after combination chemotherapy, radiotherapy or symptomatic treatmentM L Slevin, V J Harvey, B A Ponder, et al.
Pageof 14