Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Gabriella Cacchiò

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2021
First report of a homozygous mutation on exon 24 of the NOTCH3 gene in a paucisymptomatic CADASIL elderly patientMichele Ragno, Luigi Pianese, Sara Tiberi, et al.
Neuroscience Letters|July 7, 2009
High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Alessia Cappelli, Michele Ragno, Gabriella Cacchiò, et al.
Current Issues in Molecular Biology|February 24, 2023
Multiple Sclerosis: Inflammatory and Neuroglial AspectsGiulio Papiri, Giordano D'Andreamatteo, Gabriella Cacchiò, et al.
European Journal of Neurology|February 24, 2026
Chronic Ataxic Neuropathy With Disialosyl Antibodies Responsive to ZanubrutinibBenedetta Tierro, Andrea Visentin, Alessandro Salvalaggio, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 11, 2007
Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstrationFiore Manganelli, Michele Ragno, Gabriella Cacchiò, et al.
Neuropsychology|June 15, 2026
Cortical correlates of apathy in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with two different pathogenic mutations in the NOTCH3 geneNatascia De Lucia, Michele Ragno, Gabriella Cacchiò, et al.
Neurogenetics|September 2, 2011
Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL)Michele Ragno, Luigi Pianese, Michele Pinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 11, 2013
"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutationMichele Ragno, Luigi Pianese, Manrico Morroni, et al.
Stroke|February 16, 2013
Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutationMichele Ragno, Alfonso Berbellini, Gabriella Cacchiò, et al.
Neuroscience Letters|November 15, 2011
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutationMichele Ragno, Luigi Pianese, Gabriella Cacchiò, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2021
First report of a homozygous mutation on exon 24 of the NOTCH3 gene in a paucisymptomatic CADASIL elderly patientMichele Ragno, Luigi Pianese, Sara Tiberi, et al.
Neuroscience Letters|July 7, 2009
High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Alessia Cappelli, Michele Ragno, Gabriella Cacchiò, et al.
Current Issues in Molecular Biology|February 24, 2023
Multiple Sclerosis: Inflammatory and Neuroglial AspectsGiulio Papiri, Giordano D'Andreamatteo, Gabriella Cacchiò, et al.
European Journal of Neurology|February 24, 2026
Chronic Ataxic Neuropathy With Disialosyl Antibodies Responsive to ZanubrutinibBenedetta Tierro, Andrea Visentin, Alessandro Salvalaggio, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 11, 2007
Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstrationFiore Manganelli, Michele Ragno, Gabriella Cacchiò, et al.
Neuropsychology|June 15, 2026
Cortical correlates of apathy in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with two different pathogenic mutations in the NOTCH3 geneNatascia De Lucia, Michele Ragno, Gabriella Cacchiò, et al.
Neurogenetics|September 2, 2011
Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL)Michele Ragno, Luigi Pianese, Michele Pinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 11, 2013
"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutationMichele Ragno, Luigi Pianese, Manrico Morroni, et al.
Stroke|February 16, 2013
Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutationMichele Ragno, Alfonso Berbellini, Gabriella Cacchiò, et al.
Neuroscience Letters|November 15, 2011
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutationMichele Ragno, Luigi Pianese, Gabriella Cacchiò, et al.
Pageof 2