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BMC Neurology
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April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation
Simone Scarcella, Laura Dell'Arti, Delia Gagliardi, 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> Gene
Francesca 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 Literature
Delia Gagliardi, Irene Faravelli, Luisa Villa, et al.
Journal of the Neurological Sciences
|
December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families
Michela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
Frontiers in Neurology
|
October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the Literature
Oscar Borsani, Daniela Piga, Stefania Costa, et al.
BMC Neurology
|
March 19, 2026
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy
Simona Zanotti, Dario Ronchi, Laura Napoli, et al.
Neurology. Genetics
|
October 16, 2020
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the <i>ND5</i> gene
Roberta Brusa, Eleonora Mauri, Laura Dell'Arti, et al.
Experimental Cell Research
|
March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neurons
Stefania Corti, Monica Nizzardo, Chiara Simone, et al.
BMC Neurology
|
September 26, 2015
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases
Francesca Magri, Irene Colombo, Roberto Del Bo, et al.
Acta Neuropathologica Communications
|
April 9, 2022
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy
Michela Ripolone, Daniele Velardo, Stefania Mondello, et al.
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of 18
Search research articles
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Showing results (91-100 of 174) with videos related to
Sort By:
Page
of 18
BMC Neurology
|
April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation
Simone Scarcella, Laura Dell'Arti, Delia Gagliardi, 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> Gene
Francesca 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 Literature
Delia Gagliardi, Irene Faravelli, Luisa Villa, et al.
Journal of the Neurological Sciences
|
December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families
Michela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
Frontiers in Neurology
|
October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the Literature
Oscar Borsani, Daniela Piga, Stefania Costa, et al.
BMC Neurology
|
March 19, 2026
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy
Simona Zanotti, Dario Ronchi, Laura Napoli, et al.
Neurology. Genetics
|
October 16, 2020
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the <i>ND5</i> gene
Roberta Brusa, Eleonora Mauri, Laura Dell'Arti, et al.
Experimental Cell Research
|
March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neurons
Stefania Corti, Monica Nizzardo, Chiara Simone, et al.
BMC Neurology
|
September 26, 2015
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases
Francesca Magri, Irene Colombo, Roberto Del Bo, et al.
Acta Neuropathologica Communications
|
April 9, 2022
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy
Michela Ripolone, Daniele Velardo, Stefania Mondello, et al.
Page
of 18