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Davide Pareyson

Showing results (1-10 of 231) with videos related to

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Journal of Neurology|February 8, 2003
Diagnosis of hereditary neuropathies in adult patientsDavide Pareyson
Neurology|May 16, 2007
Axonal Charcot-Marie-Tooth disease: the fog is only slowly liftingDavide Pareyson
Neuromuscular Disorders : NMD|July 16, 2023
Gene therapy and other novel treatment approaches for Charcot-Marie-Tooth diseaseChiara Pisciotta, Davide Pareyson
Journal of Neurology, Neurosurgery, and Psychiatry|December 10, 2023
The tip of the iceberg in ATTRv: when to start carrier monitoring and when to initiate treatment?Davide Pareyson, Silvia Fenu
Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
CMT2CC associated with <i>NEFH</i> mutations: a predominantly motor neuronopathyChiara Pisciotta, Davide Pareyson
The Lancet. Neurology|October 13, 2009
Charcot-Marie-Tooth disease type 1A: is ascorbic acid effective?Davide Pareyson, Alessandra Solari
Advances in Experimental Medicine and Biology|March 13, 2010
Natural history and treatment of peripheral inherited neuropathiesDavide Pareyson, Chiara Marchesi
The Lancet. Neurology|June 23, 2009
Diagnosis, natural history, and management of Charcot-Marie-Tooth diseaseDavide Pareyson, Chiara Marchesi
Journal of Neurology|July 24, 2012
Clinical neurogenetics: recent advancesDavide Pareyson, Ettore Salsano
Journal of the Peripheral Nervous System : JPNS|June 7, 2022
Charcot-Marie-Tooth disease in AfricaStephan Züchner, Davide Pareyson
Pageof 24

Showing results (1-10 of 231) with videos related to

Sort By:
Pageof 24
Journal of Neurology|February 8, 2003
Diagnosis of hereditary neuropathies in adult patientsDavide Pareyson
Neurology|May 16, 2007
Axonal Charcot-Marie-Tooth disease: the fog is only slowly liftingDavide Pareyson
Neuromuscular Disorders : NMD|July 16, 2023
Gene therapy and other novel treatment approaches for Charcot-Marie-Tooth diseaseChiara Pisciotta, Davide Pareyson
Journal of Neurology, Neurosurgery, and Psychiatry|December 10, 2023
The tip of the iceberg in ATTRv: when to start carrier monitoring and when to initiate treatment?Davide Pareyson, Silvia Fenu
Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
CMT2CC associated with <i>NEFH</i> mutations: a predominantly motor neuronopathyChiara Pisciotta, Davide Pareyson
The Lancet. Neurology|October 13, 2009
Charcot-Marie-Tooth disease type 1A: is ascorbic acid effective?Davide Pareyson, Alessandra Solari
Advances in Experimental Medicine and Biology|March 13, 2010
Natural history and treatment of peripheral inherited neuropathiesDavide Pareyson, Chiara Marchesi
The Lancet. Neurology|June 23, 2009
Diagnosis, natural history, and management of Charcot-Marie-Tooth diseaseDavide Pareyson, Chiara Marchesi
Journal of Neurology|July 24, 2012
Clinical neurogenetics: recent advancesDavide Pareyson, Ettore Salsano
Journal of the Peripheral Nervous System : JPNS|June 7, 2022
Charcot-Marie-Tooth disease in AfricaStephan Züchner, Davide Pareyson
Pageof 24