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M Povedano

Showing results (11-20 of 17) with videos related to

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Neuropathology and Applied Neurobiology|February 14, 1998
Expression of myogenic regulatory factors (MRFs) in human neuromuscular disordersM Olivé, J A Martinez-Matos, P Pirretas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2006
Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusisR Reñé, J Campdelacreu, I Ferrer, et al.
Pain Management|November 20, 2018
Observational pilot study of patients with carpal tunnel syndrome treated with Nucleo CMP Forte™M Povedano, Y Martínez, A Tejado, et al.
BMJ Case Reports|July 8, 2011
Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusisR Reñé, J Campdelacreu, I Ferrer, et al.
Revista De Neurologia|October 26, 2022
[Access to orphan drugs for the treatment of spinal muscular atrophy in Spain]B García-Parra, J M Guiu, P Modamio, et al.
Neurology|October 10, 2002
The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathyR Rojas-García, E Tizzano, I Cuscó, et al.
Neurologia|March 4, 2022
Delphi consensus on recommendations for the treatment of spinal muscular atrophy in Spain (RET-AME consensus)I Pitarch Castellano, M Cabrera-Serrano, R Calvo Medina, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Neuropathology and Applied Neurobiology|February 14, 1998
Expression of myogenic regulatory factors (MRFs) in human neuromuscular disordersM Olivé, J A Martinez-Matos, P Pirretas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2006
Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusisR Reñé, J Campdelacreu, I Ferrer, et al.
Pain Management|November 20, 2018
Observational pilot study of patients with carpal tunnel syndrome treated with Nucleo CMP Forte™M Povedano, Y Martínez, A Tejado, et al.
BMJ Case Reports|July 8, 2011
Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusisR Reñé, J Campdelacreu, I Ferrer, et al.
Revista De Neurologia|October 26, 2022
[Access to orphan drugs for the treatment of spinal muscular atrophy in Spain]B García-Parra, J M Guiu, P Modamio, et al.
Neurology|October 10, 2002
The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathyR Rojas-García, E Tizzano, I Cuscó, et al.
Neurologia|March 4, 2022
Delphi consensus on recommendations for the treatment of spinal muscular atrophy in Spain (RET-AME consensus)I Pitarch Castellano, M Cabrera-Serrano, R Calvo Medina, et al.
Pageof 2