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Raffaele Lodi

Showing results (101-110 of 180) with videos related to

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Brain Research Bulletin|July 21, 2015
Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophyStefano Zanigni, Rossana Terlizzi, Caterina Tonon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2011
Brain diffusion-weighted imaging in Friedreich's ataxiaGiovanni Rizzo, Caterina Tonon, Maria Lucia Valentino, et al.
Neuroimage. Clinical|April 27, 2023
Cognitive and functional connectivity impairment in post-COVID-19 olfactory dysfunctionLorenzo Muccioli, Giovanni Sighinolfi, Micaela Mitolo, et al.
Annals of Neurology|October 27, 2004
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathyMaria Lucia Valentino, Piero Barboni, Anna Ghelli, et al.
Archives of Neurology|April 13, 2005
Antioxidant treatment of patients with Friedreich ataxia: four-year follow-upPaul E Hart, Raffaele Lodi, Bheeshma Rajagopalan, et al.
Biochemical Pharmacology|March 1, 2021
Brain functional MRI responses to blue light stimulation in Leber's hereditary optic neuropathyStefania Evangelisti, Chiara La Morgia, Claudia Testa, et al.
Parkinsonism & Related Disorders|March 15, 2017
White matter and cortical changes in atypical parkinsonisms: A multimodal quantitative MR studyStefano Zanigni, Stefania Evangelisti, Claudia Testa, et al.
Neuromuscular Disorders : NMD|January 1, 2018
Mitochondrial dysfunction in myotonic dystrophy type 1Laura Ludovica Gramegna, Maria Pia Giannoccaro, David Neil Manners, et al.
BMC Neurology|June 3, 2014
Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesionsChiara La Morgia, Leonardo Caporali, Francesca Gandini, et al.
Brain : a Journal of Neurology|September 17, 2009
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy studyRaffaele Lodi, Piero Parchi, Caterina Tonon, et al.
Pageof 18

Showing results (101-110 of 180) with videos related to

Sort By:
Pageof 18
Brain Research Bulletin|July 21, 2015
Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophyStefano Zanigni, Rossana Terlizzi, Caterina Tonon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2011
Brain diffusion-weighted imaging in Friedreich's ataxiaGiovanni Rizzo, Caterina Tonon, Maria Lucia Valentino, et al.
Neuroimage. Clinical|April 27, 2023
Cognitive and functional connectivity impairment in post-COVID-19 olfactory dysfunctionLorenzo Muccioli, Giovanni Sighinolfi, Micaela Mitolo, et al.
Annals of Neurology|October 27, 2004
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathyMaria Lucia Valentino, Piero Barboni, Anna Ghelli, et al.
Archives of Neurology|April 13, 2005
Antioxidant treatment of patients with Friedreich ataxia: four-year follow-upPaul E Hart, Raffaele Lodi, Bheeshma Rajagopalan, et al.
Biochemical Pharmacology|March 1, 2021
Brain functional MRI responses to blue light stimulation in Leber's hereditary optic neuropathyStefania Evangelisti, Chiara La Morgia, Claudia Testa, et al.
Parkinsonism & Related Disorders|March 15, 2017
White matter and cortical changes in atypical parkinsonisms: A multimodal quantitative MR studyStefano Zanigni, Stefania Evangelisti, Claudia Testa, et al.
Neuromuscular Disorders : NMD|January 1, 2018
Mitochondrial dysfunction in myotonic dystrophy type 1Laura Ludovica Gramegna, Maria Pia Giannoccaro, David Neil Manners, et al.
BMC Neurology|June 3, 2014
Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesionsChiara La Morgia, Leonardo Caporali, Francesca Gandini, et al.
Brain : a Journal of Neurology|September 17, 2009
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy studyRaffaele Lodi, Piero Parchi, Caterina Tonon, et al.
Pageof 18