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R Del Bo

Showing results (31-40 of 37) with videos related to

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Rejuvenation Research|July 22, 2010
TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease courseB Borroni, S Archetti, R Del Bo, et al.
European Journal of Neurology|November 27, 2019
Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophyV Galimberti, R Tironi, A Lerario, et al.
Experimental Cell Research|June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouseS Corti, S Strazzer, R Del Bo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
European Journal of Neurology|February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutationsR Del Bo, S Ghezzi, S Corti, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Rejuvenation Research|July 22, 2010
TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease courseB Borroni, S Archetti, R Del Bo, et al.
European Journal of Neurology|November 27, 2019
Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophyV Galimberti, R Tironi, A Lerario, et al.
Experimental Cell Research|June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouseS Corti, S Strazzer, R Del Bo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
European Journal of Neurology|February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutationsR Del Bo, S Ghezzi, S Corti, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
Pageof 4