Showing results (51-60 of 176) with videos related to
Sort By:
Pageof 18
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.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.Current Treatment Options in Neurology|July 26, 2017
CADASIL: Treatment and Management OptionsAnna Bersano, Gloria Bedini, Joshua Oskam, et al.Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathyPatrizia Dacci, Franco Taroni, Eleonora Dalla Bella, et al.Pageof 18