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Clinical Neurology and Neurosurgery
|
February 15, 2016
The wide spectrum of cerebrotendinous xanthomatosis: Case report of a rare but treatable disease
Francesca 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 plays
Silvia 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 phenotype
Andreas 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 dropout
Stefania Magri, Lorenzo Nanetti, Alessia Mongelli, et al.
Neurogenetics
|
August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patients
Cinzia 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 hemochromatosis
Emil 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 Aspects
Stefano 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 scenarios
Franco 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 phenotype
Marta 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 evidence
Emanuele Sironi, Franco Taroni, Claudio Baldinotti, et al.
Page
of 21
Search research articles
Search
Showing results (61-70 of 204) with videos related to
Sort By:
Page
of 21
Clinical Neurology and Neurosurgery
|
February 15, 2016
The wide spectrum of cerebrotendinous xanthomatosis: Case report of a rare but treatable disease
Francesca 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 plays
Silvia 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 phenotype
Andreas 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 dropout
Stefania Magri, Lorenzo Nanetti, Alessia Mongelli, et al.
Neurogenetics
|
August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patients
Cinzia 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 hemochromatosis
Emil 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 Aspects
Stefano 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 scenarios
Franco 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 phenotype
Marta 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 evidence
Emanuele Sironi, Franco Taroni, Claudio Baldinotti, et al.
Page
of 21