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Alessandra Rufa

Showing results (61-70 of 83) with videos related to

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Cerebrovascular Diseases (Basel, Switzerland)|November 6, 2008
Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathyAlessandra Rufa, Patrizia Blardi, Arianna De Lalla, et al.
Cerebellum (London, England)|February 26, 2013
Clinical course of two Italian siblings with ataxia-telangiectasia-like disorderSilvia Palmeri, Alessandra Rufa, Barbara Pucci, et al.
Journal of Neurology|December 7, 2005
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophyElena Cardaioli, Gian Nicola Gallus, Paola Da Pozzo, et al.
Molecular Vision|February 17, 2010
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophyGian Nicola Gallus, Elena Cardaioli, Alessandra Rufa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2022
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosisDiego Lopergolo, Gianna Berti, Francesca Mari, et al.
Journal of Neurology|February 18, 2014
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R geneCarla Battisti, Ilaria Di Donato, Silvia Bianchi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
Eye movement disorders and neurological symptoms in late-onset inborn errors of metabolismLisette H Koens, Marina A J Tijssen, Fiete Lange, et al.
Journal of the Neurological Sciences|January 25, 2011
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) geneElena Cardaioli, Edoardo Malfatti, Paola Da Pozzo, et al.
Journal of the Neurological Sciences|March 23, 2015
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 genePatrizia Formichi, Elena Radi, Eleonora Giorgi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 11, 2026
Repetitive transcranial magnetic stimulation for visual snow syndrome: symptoms relief and changes in brain dynamics. A case reportFrancesco Neri, David De Monte, Alberto Benelli, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Cerebrovascular Diseases (Basel, Switzerland)|November 6, 2008
Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathyAlessandra Rufa, Patrizia Blardi, Arianna De Lalla, et al.
Cerebellum (London, England)|February 26, 2013
Clinical course of two Italian siblings with ataxia-telangiectasia-like disorderSilvia Palmeri, Alessandra Rufa, Barbara Pucci, et al.
Journal of Neurology|December 7, 2005
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophyElena Cardaioli, Gian Nicola Gallus, Paola Da Pozzo, et al.
Molecular Vision|February 17, 2010
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophyGian Nicola Gallus, Elena Cardaioli, Alessandra Rufa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2022
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosisDiego Lopergolo, Gianna Berti, Francesca Mari, et al.
Journal of Neurology|February 18, 2014
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R geneCarla Battisti, Ilaria Di Donato, Silvia Bianchi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
Eye movement disorders and neurological symptoms in late-onset inborn errors of metabolismLisette H Koens, Marina A J Tijssen, Fiete Lange, et al.
Journal of the Neurological Sciences|January 25, 2011
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) geneElena Cardaioli, Edoardo Malfatti, Paola Da Pozzo, et al.
Journal of the Neurological Sciences|March 23, 2015
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 genePatrizia Formichi, Elena Radi, Eleonora Giorgi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 11, 2026
Repetitive transcranial magnetic stimulation for visual snow syndrome: symptoms relief and changes in brain dynamics. A case reportFrancesco Neri, David De Monte, Alberto Benelli, et al.
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