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Nereo Bresolin

Showing results (271-280 of 346) with videos related to

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Plos One|January 19, 2012
A functional variant in ERAP1 predisposes to multiple sclerosisFranca Rosa Guerini, Rachele Cagliani, Diego Forni, et al.
Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.
Human Molecular Genetics|October 11, 2019
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove SyndromeGiacomo Bitetto, Dario Ronchi, Sara Bonato, et al.
Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.
Neurobiology of Aging|November 23, 2006
Absence of angiogenic genes modification in Italian ALS patientsRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Muscle & Nerve|July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, ItalyDelia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Neuroscience Letters|December 8, 2009
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypesMilena De Riz, Daniela Galimberti, Chiara Fenoglio, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Annals of Neurology|January 16, 2021
A Novel Homozygous VPS11 Variant May Cause Generalized DystoniaEdoardo Monfrini, Filippo Cogiamanian, Sabrina Salani, et al.
Neurobiology of Aging|February 19, 2005
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patientsIlaria Guidi, Daniela Galimberti, Eliana Venturelli, et al.
Pageof 35

Showing results (271-280 of 346) with videos related to

Sort By:
Pageof 35
Plos One|January 19, 2012
A functional variant in ERAP1 predisposes to multiple sclerosisFranca Rosa Guerini, Rachele Cagliani, Diego Forni, et al.
Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.
Human Molecular Genetics|October 11, 2019
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove SyndromeGiacomo Bitetto, Dario Ronchi, Sara Bonato, et al.
Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.
Neurobiology of Aging|November 23, 2006
Absence of angiogenic genes modification in Italian ALS patientsRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Muscle & Nerve|July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, ItalyDelia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Neuroscience Letters|December 8, 2009
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypesMilena De Riz, Daniela Galimberti, Chiara Fenoglio, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Annals of Neurology|January 16, 2021
A Novel Homozygous VPS11 Variant May Cause Generalized DystoniaEdoardo Monfrini, Filippo Cogiamanian, Sabrina Salani, et al.
Neurobiology of Aging|February 19, 2005
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patientsIlaria Guidi, Daniela Galimberti, Eliana Venturelli, et al.
Pageof 35