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I L Simone

Showing results (41-50 of 55) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based studyS Zoccolella, E Beghi, G Palagano, et al.
European Journal of Neurology|January 3, 2013
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegiaA Magariello, C Tortorella, A Patitucci, et al.
European Journal of Neurology|June 12, 2012
Elevated cerebrospinal fluid neurofilament light levels in patients with amyotrophic lateral sclerosis: a possible marker of disease severity and progressionR Tortelli, M Ruggieri, R Cortese, et al.
European Journal of Neurology|April 23, 2014
Cerebrospinal fluid neurofilament light chain levels: marker of progression to generalized amyotrophic lateral sclerosisR Tortelli, M Copetti, M Ruggieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 1998
Localised 1H-MR spectroscopy for metabolic characterisation of diffuse and focal brain lesions in patients infected with HIVI L Simone, F Federico, C Tortorella, et al.
European Journal of Neurology|March 27, 2016
Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational studyR Tortelli, M Copetti, F Panza, et al.
Journal of the Neurological Sciences|June 19, 2014
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafnessM Muglia, L Citrigno, E D'Errico, et al.
Neurology|December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASILM Liguori, R Mazzei, C Ungaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosisF L Conforti, W Sproviero, I L Simone, et al.
Neuromuscular Disorders : NMD|August 21, 2007
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern ItalyF L Conforti, T Sprovieri, R Mazzei, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based studyS Zoccolella, E Beghi, G Palagano, et al.
European Journal of Neurology|January 3, 2013
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegiaA Magariello, C Tortorella, A Patitucci, et al.
European Journal of Neurology|June 12, 2012
Elevated cerebrospinal fluid neurofilament light levels in patients with amyotrophic lateral sclerosis: a possible marker of disease severity and progressionR Tortelli, M Ruggieri, R Cortese, et al.
European Journal of Neurology|April 23, 2014
Cerebrospinal fluid neurofilament light chain levels: marker of progression to generalized amyotrophic lateral sclerosisR Tortelli, M Copetti, M Ruggieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 1998
Localised 1H-MR spectroscopy for metabolic characterisation of diffuse and focal brain lesions in patients infected with HIVI L Simone, F Federico, C Tortorella, et al.
European Journal of Neurology|March 27, 2016
Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational studyR Tortelli, M Copetti, F Panza, et al.
Journal of the Neurological Sciences|June 19, 2014
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafnessM Muglia, L Citrigno, E D'Errico, et al.
Neurology|December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASILM Liguori, R Mazzei, C Ungaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosisF L Conforti, W Sproviero, I L Simone, et al.
Neuromuscular Disorders : NMD|August 21, 2007
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern ItalyF L Conforti, T Sprovieri, R Mazzei, et al.
Pageof 6