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M T Dotti

Showing results (131-140 of 144) with videos related to

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Journal of Neurology|February 20, 2010
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiaritiesS Bianchi, A Rufa, M Ragno, et al.
Journal of the Neurological Sciences|July 8, 2008
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNAE Cardaioli, P Da Pozzo, E Malfatti, et al.
Journal of Neurology|April 26, 2012
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-upF Sicurelli, M A Carluccio, F Toraldo, et al.
Neurology|January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)C Bruno, E Bertini, A Federico, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesM T Dotti, A Federico, R Mazzei, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Scientific Reports|December 2, 2016
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
Scientific Reports|February 23, 2017
Erratum: Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
European Journal of Neurology|July 23, 2013
Influence of vascular risk factors and neuropsychological profile on functional performances in CADASIL: results from the MIcrovascular LEukoencephalopathy Study (MILES)L Ciolli, F Pescini, E Salvadori, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Journal of Neurology|February 20, 2010
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiaritiesS Bianchi, A Rufa, M Ragno, et al.
Journal of the Neurological Sciences|July 8, 2008
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNAE Cardaioli, P Da Pozzo, E Malfatti, et al.
Journal of Neurology|April 26, 2012
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-upF Sicurelli, M A Carluccio, F Toraldo, et al.
Neurology|January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)C Bruno, E Bertini, A Federico, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesM T Dotti, A Federico, R Mazzei, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Scientific Reports|December 2, 2016
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
Scientific Reports|February 23, 2017
Erratum: Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
European Journal of Neurology|July 23, 2013
Influence of vascular risk factors and neuropsychological profile on functional performances in CADASIL: results from the MIcrovascular LEukoencephalopathy Study (MILES)L Ciolli, F Pescini, E Salvadori, et al.
Pageof 15