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Frontiers in Neurology
|
February 2, 2024
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy
Martina Rimoldi, Gloria Romagnoli, Francesca Magri, et al.
Experimental Neurology
|
May 1, 2007
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Brain : a Journal of Neurology
|
April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model
Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Frontiers in Neurology
|
June 2, 2023
Clinical and molecular features of patients with amyotrophic lateral sclerosis and <i>SOD1</i> mutations: a monocentric study
Delia Gagliardi, Paolo Ripellino, Megi Meneri, et al.
Frontiers in Genetics
|
June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
Arianna Manini, Leonardo Caporali, Megi Meneri, et al.
BMC Neurology
|
December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye
Eleonora 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 Patient
Elena Abati, Irene Faravelli, Francesca Magri, et al.
Molecular Neurobiology
|
February 9, 2024
Shaping the Neurovascular Unit Exploiting Human Brain Organoids
Mafalda Rizzuti, Valentina Melzi, Lorenzo Brambilla, et al.
Neurology. Genetics
|
September 3, 2025
Single Nucleotide <i>SMN1</i> Variants in a Cohort of Individuals With Spinal Muscular Atrophy
Martina Rimoldi, Francesca Magri, Megi Meneri, et al.
Page
of 29
Search research articles
Search
Showing results (151-160 of 287) with videos related to
Sort By:
Page
of 29
Frontiers in Neurology
|
February 2, 2024
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy
Martina Rimoldi, Gloria Romagnoli, Francesca Magri, et al.
Experimental Neurology
|
May 1, 2007
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Brain : a Journal of Neurology
|
April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model
Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Frontiers in Neurology
|
June 2, 2023
Clinical and molecular features of patients with amyotrophic lateral sclerosis and <i>SOD1</i> mutations: a monocentric study
Delia Gagliardi, Paolo Ripellino, Megi Meneri, et al.
Frontiers in Genetics
|
June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
Arianna Manini, Leonardo Caporali, Megi Meneri, et al.
BMC Neurology
|
December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye
Eleonora 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 Patient
Elena Abati, Irene Faravelli, Francesca Magri, et al.
Molecular Neurobiology
|
February 9, 2024
Shaping the Neurovascular Unit Exploiting Human Brain Organoids
Mafalda Rizzuti, Valentina Melzi, Lorenzo Brambilla, et al.
Neurology. Genetics
|
September 3, 2025
Single Nucleotide <i>SMN1</i> Variants in a Cohort of Individuals With Spinal Muscular Atrophy
Martina Rimoldi, Francesca Magri, Megi Meneri, et al.
Page
of 29