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N Bresolin

Showing results (191-200 of 206) with videos related to

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Neurology|October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndromeA Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIaG M Hadjigeorgiou, G P Comi, A Bordoni, 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.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology|May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degenerationC Villa, E Venturelli, C Fenoglio, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Medical Genetics|February 7, 2009
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosumC Crimella, A Arnoldi, F Crippa, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Molecular Biology and Evolution|February 10, 2012
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosisR Cagliani, F R Guerini, M Fumagalli, et al.
Pageof 21

Showing results (191-200 of 206) with videos related to

Sort By:
Pageof 21
Neurology|October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndromeA Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIaG M Hadjigeorgiou, G P Comi, A Bordoni, 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.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology|May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degenerationC Villa, E Venturelli, C Fenoglio, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Medical Genetics|February 7, 2009
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosumC Crimella, A Arnoldi, F Crippa, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Molecular Biology and Evolution|February 10, 2012
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosisR Cagliani, F R Guerini, M Fumagalli, et al.
Pageof 21