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Showing results (21-30 of 31) with videos related to

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Neurology|September 25, 1999
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathyG Meola, V Sansone, D Perani, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 1, 1988
Technetium-99m HM-PAO-SPECT study of regional cerebral perfusion in early Alzheimer's diseaseD Perani, V Di Piero, G Vallar, et al.
Cognitive Processing|September 4, 2009
Gender-related differences in moral judgmentsM Fumagalli, R Ferrucci, F Mameli, et al.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)G Meola, V Sansone, D Perani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2004
Frontotemporal dementia: impact of P301L tau mutation on a healthy carrierA Alberici, C Gobbo, A Panzacchi, 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.
European Journal of Neurology|November 7, 2019
Italian consensus recommendations for a biomarker-based aetiological diagnosis in mild cognitive impairment patientsM Boccardi, V Nicolosi, C Festari, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Neurology|September 25, 1999
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathyG Meola, V Sansone, D Perani, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 1, 1988
Technetium-99m HM-PAO-SPECT study of regional cerebral perfusion in early Alzheimer's diseaseD Perani, V Di Piero, G Vallar, et al.
Cognitive Processing|September 4, 2009
Gender-related differences in moral judgmentsM Fumagalli, R Ferrucci, F Mameli, et al.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)G Meola, V Sansone, D Perani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2004
Frontotemporal dementia: impact of P301L tau mutation on a healthy carrierA Alberici, C Gobbo, A Panzacchi, 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.
European Journal of Neurology|November 7, 2019
Italian consensus recommendations for a biomarker-based aetiological diagnosis in mild cognitive impairment patientsM Boccardi, V Nicolosi, C Festari, et al.
Pageof 4