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Serena Silvestri

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

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Healthcare (Basel, Switzerland)|August 14, 2025
Mental Health Issues in Undercover Police Officers: A Systematic Literature Search from a Psychiatric PerspectiveGiulia Moretti, Lucrezia Cavagnis, Emma Flutti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 15, 2019
Maternal germline mosaicism in Fabry diseaseLuigi Pianese, Antonio Fortunato, Serena Silvestri, et al.
Diabetes Research and Clinical Practice|April 26, 2011
A new de novo mutation in the GCK gene causing MODY2Alessia Cappelli, Serena Silvestri, Stefano Tumini, et al.
Histology and Histopathology|September 1, 2012
Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-upMichele Ragno, Luigi Trojano, Luigi Pianese, 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.
Stroke|March 1, 2014
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASILChristian Opherk, Mariya Gonik, Marco Duering, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|April 30, 2015
APOE ɛ2 is associated with white matter hyperintensity volume in CADASILBenno Gesierich, Christian Opherk, Jonathan Rosand, et al.
Pageof 1

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

Sort By:
Pageof 1
Healthcare (Basel, Switzerland)|August 14, 2025
Mental Health Issues in Undercover Police Officers: A Systematic Literature Search from a Psychiatric PerspectiveGiulia Moretti, Lucrezia Cavagnis, Emma Flutti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 15, 2019
Maternal germline mosaicism in Fabry diseaseLuigi Pianese, Antonio Fortunato, Serena Silvestri, et al.
Diabetes Research and Clinical Practice|April 26, 2011
A new de novo mutation in the GCK gene causing MODY2Alessia Cappelli, Serena Silvestri, Stefano Tumini, et al.
Histology and Histopathology|September 1, 2012
Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-upMichele Ragno, Luigi Trojano, Luigi Pianese, 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.
Stroke|March 1, 2014
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASILChristian Opherk, Mariya Gonik, Marco Duering, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|April 30, 2015
APOE ɛ2 is associated with white matter hyperintensity volume in CADASILBenno Gesierich, Christian Opherk, Jonathan Rosand, et al.
Pageof 1