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Ghetti

Showing results (521-530 of 974) with videos related to

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Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|February 10, 2010
Safety, efficacy and long-term durability of endovascular therapy for carotid artery disease: the tailored-Carotid Artery Stenting Experience of a single high-volume centre (tailored-CASE Registry)Alberto Cremonesi, Shane Gieowarsingh, Barbara Spagnolo, et al.
Current Neurology and Neuroscience Reports|September 14, 2014
Genetic heterogeneity in Alzheimer disease and implications for treatment strategiesJohn M Ringman, Alison Goate, Colin L Masters, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 18, 2009
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and choreaGabor G Kovacs, Jill R Murrell, Sandor Horvath, et al.
Experimental Brain Research|January 1, 1997
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver miceT Verina, J A Norton, J J Sorbel, et al.
Radiation Protection Dosimetry|February 2, 2026
State-of-the-art 32 cm field-of-view digital PET/CT system: preliminary study for protocols optimization and DRLs updateChristian Paolo Luca Fulcheri, Ottavia Sguazzini, Veronica D'Ignoti Parenti, et al.
Brain Pathology (Zurich, Switzerland)|January 17, 2014
Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Sarah Hoffmann, Jill Murrell, Lutz Harms, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Journal of Ophthalmology|January 5, 2017
Altered Brain Glucose Consumption in Cogan's SyndromePaolo Mora, Livia Ruffini, Caterina Ghetti, et al.
Neurourology and Urodynamics|June 14, 2008
The correlation of voiding variables between non-instrumented uroflowmetery and pressure-flow studies in women with pelvic organ prolapseElizabeth Mueller, John Wei, Ingrid Nygaard, et al.
Pageof 98

Showing results (521-530 of 974) with videos related to

Sort By:
Pageof 98
Acta Neuropathologica|July 21, 1999
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsyM B Delisle, J R Murrell, R Richardson, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|February 10, 2010
Safety, efficacy and long-term durability of endovascular therapy for carotid artery disease: the tailored-Carotid Artery Stenting Experience of a single high-volume centre (tailored-CASE Registry)Alberto Cremonesi, Shane Gieowarsingh, Barbara Spagnolo, et al.
Current Neurology and Neuroscience Reports|September 14, 2014
Genetic heterogeneity in Alzheimer disease and implications for treatment strategiesJohn M Ringman, Alison Goate, Colin L Masters, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 18, 2009
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and choreaGabor G Kovacs, Jill R Murrell, Sandor Horvath, et al.
Experimental Brain Research|January 1, 1997
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver miceT Verina, J A Norton, J J Sorbel, et al.
Radiation Protection Dosimetry|February 2, 2026
State-of-the-art 32 cm field-of-view digital PET/CT system: preliminary study for protocols optimization and DRLs updateChristian Paolo Luca Fulcheri, Ottavia Sguazzini, Veronica D'Ignoti Parenti, et al.
Brain Pathology (Zurich, Switzerland)|January 17, 2014
Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Sarah Hoffmann, Jill Murrell, Lutz Harms, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Journal of Ophthalmology|January 5, 2017
Altered Brain Glucose Consumption in Cogan's SyndromePaolo Mora, Livia Ruffini, Caterina Ghetti, et al.
Neurourology and Urodynamics|June 14, 2008
The correlation of voiding variables between non-instrumented uroflowmetery and pressure-flow studies in women with pelvic organ prolapseElizabeth Mueller, John Wei, Ingrid Nygaard, et al.
Pageof 98