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Anna Sagnelli

Showing results (1-10 of 15) with videos related to

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Journal of Neurology|September 25, 2013
Inherited neuropathies: an updateAnna Sagnelli, Giuseppe Piscosquito, Davide Pareyson
Neuroscience Letters|April 8, 2015
Mitochondrial dynamics and inherited peripheral nerve diseasesDavide Pareyson, Paola Saveri, Anna Sagnelli, et al.
Neuromuscular Disorders : NMD|August 24, 2015
Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patientAnna Sagnelli, Vidmer Scaioli, Giuseppe Piscosquito, et al.
Journal of Molecular Neuroscience : MN|November 18, 2015
Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and FuturePatrick Weydt, Anna Sagnelli, Angela Rosenbohm, et al.
Case Reports in Medicine|January 18, 2013
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case reportFrancesca Trojsi, Anna Sagnelli, Giovanni Cirillo, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsyAnna Sagnelli, Giuseppe Piscosquito, Daniela Di Bella, et al.
Annali Dell'Istituto Superiore Di Sanita|September 26, 2012
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian databaseFrancesca Trojsi, Anna Sagnelli, Nicola Vanacore, et al.
Neurobiology of Aging|August 27, 2010
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosisGioacchino Tedeschi, Francesca Trojsi, Alessandro Tessitore, et al.
Journal of Molecular Neuroscience : MN|January 9, 2016
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular AtrophyDavide Pareyson, Pietro Fratta, Pierre-François Pradat, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Neurology|September 25, 2013
Inherited neuropathies: an updateAnna Sagnelli, Giuseppe Piscosquito, Davide Pareyson
Neuroscience Letters|April 8, 2015
Mitochondrial dynamics and inherited peripheral nerve diseasesDavide Pareyson, Paola Saveri, Anna Sagnelli, et al.
Neuromuscular Disorders : NMD|August 24, 2015
Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patientAnna Sagnelli, Vidmer Scaioli, Giuseppe Piscosquito, et al.
Journal of Molecular Neuroscience : MN|November 18, 2015
Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and FuturePatrick Weydt, Anna Sagnelli, Angela Rosenbohm, et al.
Case Reports in Medicine|January 18, 2013
Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case reportFrancesca Trojsi, Anna Sagnelli, Giovanni Cirillo, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsyAnna Sagnelli, Giuseppe Piscosquito, Daniela Di Bella, et al.
Annali Dell'Istituto Superiore Di Sanita|September 26, 2012
Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian databaseFrancesca Trojsi, Anna Sagnelli, Nicola Vanacore, et al.
Neurobiology of Aging|August 27, 2010
Interaction between aging and neurodegeneration in amyotrophic lateral sclerosisGioacchino Tedeschi, Francesca Trojsi, Alessandro Tessitore, et al.
Journal of Molecular Neuroscience : MN|January 9, 2016
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular AtrophyDavide Pareyson, Pietro Fratta, Pierre-François Pradat, et al.
Pageof 2