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

Nereo Bresolin

Showing results (201-210 of 346) with videos related to

Pageof 35
Sort By:
Genome Biology|November 1, 2014
Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disordersDiego Forni, Uberto Pozzoli, Rachele Cagliani, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Immunogenetics|March 2, 2006
VEGF gene variability and type 1 diabetes: evidence for a protective roleRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, 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.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.
Frontiers in Neurology|December 18, 2018
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientElena Abati, Irene Faravelli, Francesca Magri, 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.
Pageof 35

Showing results (201-210 of 346) with videos related to

Sort By:
Pageof 35
Genome Biology|November 1, 2014
Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disordersDiego Forni, Uberto Pozzoli, Rachele Cagliani, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Immunogenetics|March 2, 2006
VEGF gene variability and type 1 diabetes: evidence for a protective roleRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, 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.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.
Frontiers in Neurology|December 18, 2018
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientElena Abati, Irene Faravelli, Francesca Magri, 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.
Pageof 35