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Raffaele Lodi

Showing results (141-150 of 180) with videos related to

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Scientific Reports|October 13, 2023
Differential diagnosis of neurodegenerative dementias with the explainable MRI based machine learning algorithm MUQUBIASilvia De Francesco, Claudio Crema, Damiano Archetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 21, 2024
Magnetic resonance imaging scoring system of the lower limbs in adult patients with suspected idiopathic inflammatory myopathyLaura Ludovica Gramegna, Rita Rinaldi, Laura Maria Beatrice Belotti, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic VariantValentina Barone, Chiara La Morgia, Leonardo Caporali, et al.
Radiology|July 27, 2007
Prostate cancer: sextant localization with MR imaging, MR spectroscopy, and 11C-choline PET/CTClaudia Testa, Riccardo Schiavina, Raffaele Lodi, et al.
Molecular Genetics and Metabolism|December 17, 2021
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutationStefania Evangelisti, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Biomedicines|October 29, 2025
Gender- and Grade-Dependent Activation of Androgen Receptor Signaling in Adult-Type Diffuse Gliomas: Epigenetic Insights from a Retrospective Cohort StudyLidia Gatto, Sofia Asioli, Luca Morandi, et al.
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
Diagnostics (Basel, Switzerland)|November 27, 2024
Detection of Brain-Derived Cell-Free DNA in PlasmaCamilla Pellegrini, Francesco Ravaioli, Sara De Fanti, et al.
Annals of Clinical and Translational Neurology|May 5, 2021
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutationsLaura L Gramegna, Stefania Evangelisti, Lidia Di Vito, et al.
EMBO Molecular Medicine|April 15, 2015
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathyTommaso Pippucci, Alessandra Maresca, Pamela Magini, et al.
Pageof 18

Showing results (141-150 of 180) with videos related to

Sort By:
Pageof 18
Scientific Reports|October 13, 2023
Differential diagnosis of neurodegenerative dementias with the explainable MRI based machine learning algorithm MUQUBIASilvia De Francesco, Claudio Crema, Damiano Archetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 21, 2024
Magnetic resonance imaging scoring system of the lower limbs in adult patients with suspected idiopathic inflammatory myopathyLaura Ludovica Gramegna, Rita Rinaldi, Laura Maria Beatrice Belotti, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic VariantValentina Barone, Chiara La Morgia, Leonardo Caporali, et al.
Radiology|July 27, 2007
Prostate cancer: sextant localization with MR imaging, MR spectroscopy, and 11C-choline PET/CTClaudia Testa, Riccardo Schiavina, Raffaele Lodi, et al.
Molecular Genetics and Metabolism|December 17, 2021
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutationStefania Evangelisti, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Biomedicines|October 29, 2025
Gender- and Grade-Dependent Activation of Androgen Receptor Signaling in Adult-Type Diffuse Gliomas: Epigenetic Insights from a Retrospective Cohort StudyLidia Gatto, Sofia Asioli, Luca Morandi, et al.
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
Diagnostics (Basel, Switzerland)|November 27, 2024
Detection of Brain-Derived Cell-Free DNA in PlasmaCamilla Pellegrini, Francesco Ravaioli, Sara De Fanti, et al.
Annals of Clinical and Translational Neurology|May 5, 2021
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutationsLaura L Gramegna, Stefania Evangelisti, Lidia Di Vito, et al.
EMBO Molecular Medicine|April 15, 2015
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathyTommaso Pippucci, Alessandra Maresca, Pamela Magini, et al.
Pageof 18