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

Franco Taroni

Showing results (61-70 of 204) with videos related to

Pageof 21
Sort By:
Clinical Neurology and Neurosurgery|February 15, 2016
The wide spectrum of cerebrotendinous xanthomatosis: Case report of a rare but treatable diseaseFrancesca Rosafio, Francesco Cavallieri, Pietro Guaraldi, et al.
Scientific Reports|November 19, 2025
The Bayes factor to discriminate Molière and Corneille as authors of classical French playsSilvia Bozza, Valentina Cammarota, Claude-Alain Roten, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2006
Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotypeAndreas J Steck, Beat Erne, Davide Pareyson, et al.
American Journal of Medical Genetics. Part A|November 28, 2020
Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropoutStefania Magri, Lorenzo Nanetti, Alessia Mongelli, et al.
Neurogenetics|August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patientsCinzia Gellera, Barbara Castellotti, Caterina Mariotti, et al.
Parkinsonism & Related Disorders|May 13, 2014
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosisEmil Ygland, Franco Taroni, Cinzia Gellera, et al.
Neuropediatrics|December 1, 2019
A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic AspectsStefano D'Arrigo, Valeria Tessarollo, Franco Taroni, et al.
International Journal of Legal Medicine|March 16, 2026
A Bayesian decision approach to classify crime scene observations in sharp-force fatalities: a study on suicide vs. homicide scenariosFranco Taroni, Silvia Bozza, Guido Pelletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2021
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotypeMarta Gatti, Stefania Magri, Daniela Di Bella, et al.
International Journal of Legal Medicine|November 16, 2017
Age estimation by assessment of pulp chamber volume: a Bayesian network for the evaluation of dental evidenceEmanuele Sironi, Franco Taroni, Claudio Baldinotti, et al.
Pageof 21

Showing results (61-70 of 204) with videos related to

Sort By:
Pageof 21
Clinical Neurology and Neurosurgery|February 15, 2016
The wide spectrum of cerebrotendinous xanthomatosis: Case report of a rare but treatable diseaseFrancesca Rosafio, Francesco Cavallieri, Pietro Guaraldi, et al.
Scientific Reports|November 19, 2025
The Bayes factor to discriminate Molière and Corneille as authors of classical French playsSilvia Bozza, Valentina Cammarota, Claude-Alain Roten, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2006
Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotypeAndreas J Steck, Beat Erne, Davide Pareyson, et al.
American Journal of Medical Genetics. Part A|November 28, 2020
Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropoutStefania Magri, Lorenzo Nanetti, Alessia Mongelli, et al.
Neurogenetics|August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patientsCinzia Gellera, Barbara Castellotti, Caterina Mariotti, et al.
Parkinsonism & Related Disorders|May 13, 2014
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosisEmil Ygland, Franco Taroni, Cinzia Gellera, et al.
Neuropediatrics|December 1, 2019
A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic AspectsStefano D'Arrigo, Valeria Tessarollo, Franco Taroni, et al.
International Journal of Legal Medicine|March 16, 2026
A Bayesian decision approach to classify crime scene observations in sharp-force fatalities: a study on suicide vs. homicide scenariosFranco Taroni, Silvia Bozza, Guido Pelletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2021
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotypeMarta Gatti, Stefania Magri, Daniela Di Bella, et al.
International Journal of Legal Medicine|November 16, 2017
Age estimation by assessment of pulp chamber volume: a Bayesian network for the evaluation of dental evidenceEmanuele Sironi, Franco Taroni, Claudio Baldinotti, et al.
Pageof 21