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Maura Brunetti

Showing results (11-20 of 86) with videos related to

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JAMA Neurology|February 24, 2016
The Role of APOE in the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral SclerosisAdriano Chiò, Maura Brunetti, Marco Barberis, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 29, 2012
An ALS case with a novel D90N-SOD1 heterozygous missense mutationAndrea Calvo, Antonio Ilardi, Cristina Moglia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2014
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year courseAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 23, 2014
Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitorAntonio Canosa, Andrea Calvo, Marco Barberis, et al.
Neurobiology of Aging|January 21, 2014
De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis caseAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Neurobiology of Aging|July 6, 2010
A de novo missense mutation of the FUS gene in a "true" sporadic ALS caseAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 28, 2002
Biweekly chemotherapy with oxaliplatin, irinotecan, infusional Fluorouracil, and leucovorin: a pilot study in patients with metastatic colorectal cancerAlfredo Falcone, Gianluca Masi, Giacomo Allegrini, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutationAntonio Canosa, Maurizio Grassano, Marco Barberis, et al.
Muscle & Nerve|March 26, 2017
Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based studyAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 29, 2014
Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in ItalyAnna Montuschi, Barbara Iazzolino, Andrea Calvo, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
JAMA Neurology|February 24, 2016
The Role of APOE in the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral SclerosisAdriano Chiò, Maura Brunetti, Marco Barberis, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 29, 2012
An ALS case with a novel D90N-SOD1 heterozygous missense mutationAndrea Calvo, Antonio Ilardi, Cristina Moglia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2014
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year courseAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 23, 2014
Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitorAntonio Canosa, Andrea Calvo, Marco Barberis, et al.
Neurobiology of Aging|January 21, 2014
De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis caseAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Neurobiology of Aging|July 6, 2010
A de novo missense mutation of the FUS gene in a "true" sporadic ALS caseAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 28, 2002
Biweekly chemotherapy with oxaliplatin, irinotecan, infusional Fluorouracil, and leucovorin: a pilot study in patients with metastatic colorectal cancerAlfredo Falcone, Gianluca Masi, Giacomo Allegrini, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutationAntonio Canosa, Maurizio Grassano, Marco Barberis, et al.
Muscle & Nerve|March 26, 2017
Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based studyAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 29, 2014
Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in ItalyAnna Montuschi, Barbara Iazzolino, Andrea Calvo, et al.
Pageof 9