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

Mario Sabatelli

Showing results (51-60 of 179) with videos related to

Pageof 18
Sort By:
Molecular Genetics and Metabolism|January 26, 2007
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutation causing a double pathogenic effectMassimo Santoro, Anna Modoni, Mario Sabatelli, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 21, 2011
A novel L67P SOD1 mutation in an Italian ALS patientAlessandra del Grande, Marco Luigetti, Amelia Conte, et al.
Genes|July 2, 2021
Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential BiomarkersAngelo Maria Minnella, Roberta Rissotto, Martina Maceroni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 30, 2022
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experienceMarco Luigetti, Andrea Di Paolantonio, Valeria Guglielmino, et al.
Clinical Neurology and Neurosurgery|June 7, 2016
Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71]Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Neuroscience Letters|September 19, 2006
Repetitive transcranial magnetic stimulation for ALS. A preliminary controlled studyVincenzo Di Lazzaro, Michele Dileone, Fabio Pilato, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosisMarco Luigetti, Francesca Madia, Amelia Conte, et al.
Clinical Neurology and Neurosurgery|March 19, 2016
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experienceMarco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Plos One|March 8, 2013
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patientsCamilla Bernardini, Federica Censi, Wanda Lattanzi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|January 15, 2019
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian CentreMarco Luigetti, Giulia Bisogni, Angela Romano, et al.
Pageof 18

Showing results (51-60 of 179) with videos related to

Sort By:
Pageof 18
Molecular Genetics and Metabolism|January 26, 2007
Chronic GM2 gangliosidosis type Sandhoff associated with a novel missense HEXB gene mutation causing a double pathogenic effectMassimo Santoro, Anna Modoni, Mario Sabatelli, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 21, 2011
A novel L67P SOD1 mutation in an Italian ALS patientAlessandra del Grande, Marco Luigetti, Amelia Conte, et al.
Genes|July 2, 2021
Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential BiomarkersAngelo Maria Minnella, Roberta Rissotto, Martina Maceroni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 30, 2022
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experienceMarco Luigetti, Andrea Di Paolantonio, Valeria Guglielmino, et al.
Clinical Neurology and Neurosurgery|June 7, 2016
Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71]Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Neuroscience Letters|September 19, 2006
Repetitive transcranial magnetic stimulation for ALS. A preliminary controlled studyVincenzo Di Lazzaro, Michele Dileone, Fabio Pilato, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosisMarco Luigetti, Francesca Madia, Amelia Conte, et al.
Clinical Neurology and Neurosurgery|March 19, 2016
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experienceMarco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Plos One|March 8, 2013
Mitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patientsCamilla Bernardini, Federica Censi, Wanda Lattanzi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|January 15, 2019
Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian CentreMarco Luigetti, Giulia Bisogni, Angela Romano, et al.
Pageof 18