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European Journal of Histochemistry : EJH
|
September 1, 2022
Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy
Simona Zanotti, Francesca Magri, Francesca Poggetti, et al.
Frontiers in Cellular Neuroscience
|
March 26, 2025
Riboflavin transporter deficiency: <i>AAV9-SLC52A2</i> gene therapy as a new therapeutic strategy
Cecilia Mei, Valentina Magliocca, Xin Chen, et al.
Human Molecular Genetics
|
September 6, 2013
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model
Monica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Journal of the Neurological Sciences
|
March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study
Roberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Medicine
|
October 30, 2020
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature
Gianluca Costamagna, Megi Meneri, Elena Abati, et al.
Scientific Reports
|
July 1, 2015
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches
Monica Nizzardo, Chiara Simone, Sara Dametti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 14, 2025
iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposure
Gioia Cappelletti, Lorenzo Brambilla, Sergio Strizzi, et al.
Cellular and Molecular Life Sciences : CMLS
|
December 26, 2024
Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA models
Elisa Pagliari, Michela Taiana, Paolo Manzini, et al.
Frontiers in Neurology
|
August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis
Roberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Biochimica Et Biophysica Acta
|
August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse model
Serena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Page
of 29
Search research articles
Search
Showing results (141-150 of 287) with videos related to
Sort By:
Page
of 29
European Journal of Histochemistry : EJH
|
September 1, 2022
Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy
Simona Zanotti, Francesca Magri, Francesca Poggetti, et al.
Frontiers in Cellular Neuroscience
|
March 26, 2025
Riboflavin transporter deficiency: <i>AAV9-SLC52A2</i> gene therapy as a new therapeutic strategy
Cecilia Mei, Valentina Magliocca, Xin Chen, et al.
Human Molecular Genetics
|
September 6, 2013
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model
Monica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Journal of the Neurological Sciences
|
March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study
Roberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Medicine
|
October 30, 2020
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature
Gianluca Costamagna, Megi Meneri, Elena Abati, et al.
Scientific Reports
|
July 1, 2015
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches
Monica Nizzardo, Chiara Simone, Sara Dametti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 14, 2025
iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposure
Gioia Cappelletti, Lorenzo Brambilla, Sergio Strizzi, et al.
Cellular and Molecular Life Sciences : CMLS
|
December 26, 2024
Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA models
Elisa Pagliari, Michela Taiana, Paolo Manzini, et al.
Frontiers in Neurology
|
August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis
Roberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Biochimica Et Biophysica Acta
|
August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse model
Serena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Page
of 29