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

Cristoforo Comi

Showing results (101-110 of 149) with videos related to

Pageof 15
Sort By:
Neurogenetics|January 20, 2021
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case seriesLuca Magistrelli, Roberta Croce, Fabiola De Marchi, et al.
Journal of Neuroimmunology|June 28, 2005
E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosisDaniela Galimberti, Chiara Fenoglio, Raffaella Clerici, et al.
Journal of the Neurological Sciences|August 18, 2009
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's diseaseMiryam Carecchio, Chiara Fenoglio, Milena De Riz, et al.
Neurology International|July 25, 2025
The Association of Axonal Damage Biomarkers and Osteopontin at Diagnosis Could Be Useful in Newly Diagnosed MS PatientsEleonora Virgilio, Chiara Puricelli, Nausicaa Clemente, et al.
Neuroimage. Clinical|October 12, 2022
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriersGiacomo Tondo, Letizia Mazzini, Silvia Paola Caminiti, et al.
Neurorehabilitation and Neural Repair|November 12, 2013
Intensive rehabilitation increases BDNF serum levels in parkinsonian patients: a randomized studyGiuseppe Frazzitta, Roberto Maestri, Maria Felice Ghilardi, et al.
Journal of the Neurological Sciences|October 31, 2007
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple SclerosisDaniela Galimberti, Diego Scalabrini, Chiara Fenoglio, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
Neuroscience Letters|July 26, 2005
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosisDiego Scalabrini, Daniela Galimberti, Chiara Fenoglio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2013
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteriaMiryam Carecchio, Monia Magliozzi, Massimiliano Copetti, et al.
Pageof 15

Showing results (101-110 of 149) with videos related to

Sort By:
Pageof 15
Neurogenetics|January 20, 2021
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case seriesLuca Magistrelli, Roberta Croce, Fabiola De Marchi, et al.
Journal of Neuroimmunology|June 28, 2005
E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosisDaniela Galimberti, Chiara Fenoglio, Raffaella Clerici, et al.
Journal of the Neurological Sciences|August 18, 2009
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's diseaseMiryam Carecchio, Chiara Fenoglio, Milena De Riz, et al.
Neurology International|July 25, 2025
The Association of Axonal Damage Biomarkers and Osteopontin at Diagnosis Could Be Useful in Newly Diagnosed MS PatientsEleonora Virgilio, Chiara Puricelli, Nausicaa Clemente, et al.
Neuroimage. Clinical|October 12, 2022
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriersGiacomo Tondo, Letizia Mazzini, Silvia Paola Caminiti, et al.
Neurorehabilitation and Neural Repair|November 12, 2013
Intensive rehabilitation increases BDNF serum levels in parkinsonian patients: a randomized studyGiuseppe Frazzitta, Roberto Maestri, Maria Felice Ghilardi, et al.
Journal of the Neurological Sciences|October 31, 2007
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple SclerosisDaniela Galimberti, Diego Scalabrini, Chiara Fenoglio, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
Neuroscience Letters|July 26, 2005
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosisDiego Scalabrini, Daniela Galimberti, Chiara Fenoglio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2013
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteriaMiryam Carecchio, Monia Magliozzi, Massimiliano Copetti, et al.
Pageof 15