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Franco Taroni

Showing results (91-100 of 204) with videos related to

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American Journal of Medical Genetics. Part A|August 23, 2019
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutationsMarta Gatti, Stefania Magri, Lorenzo Nanetti, et al.
Talanta|October 31, 2008
Chemical profiling and classification of illicit heroin by principal component analysis, calculation of inter sample correlation and artificial neural networksPierre Esseiva, Frederic Anglada, Laurence Dujourdy, et al.
Neurobiology of Aging|March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counselingCinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neuroscience Letters|May 2, 2018
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patientsAlessia Mongelli, Lidia Sarro, Elena Rizzo, et al.
Journal of the Neurological Sciences|May 1, 2019
Neuropsychological features of adult form of Alexander diseaseLara Draghi, Ettore Salsano, Laura Farina, et al.
Journal of Forensic Sciences|August 8, 2015
A Practical Guide for the Formulation of Propositions in the Bayesian Approach to DNA Evidence Interpretation in an Adversarial EnvironmentSimone Gittelson, Tim Kalafut, Steven Myers, et al.
Journal of Neuromuscular Diseases|May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literatureElena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.
Frontiers in Genetics|December 27, 2016
Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent ConcernsAlex Biedermann, Christophe Champod, Graham Jackson, et al.
Journal of Neurochemistry|March 16, 2026
Neurotrophic Modulation Restores Motor and Developmental Defects in Zebrafish Models of ints11 DeficiencyAnna Pistocchi, Elena Chiricozzi, Matilde Molteni, et al.
Experimental Neurology|March 18, 2009
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interferenceMaria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, et al.
Pageof 21

Showing results (91-100 of 204) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics. Part A|August 23, 2019
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutationsMarta Gatti, Stefania Magri, Lorenzo Nanetti, et al.
Talanta|October 31, 2008
Chemical profiling and classification of illicit heroin by principal component analysis, calculation of inter sample correlation and artificial neural networksPierre Esseiva, Frederic Anglada, Laurence Dujourdy, et al.
Neurobiology of Aging|March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counselingCinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neuroscience Letters|May 2, 2018
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patientsAlessia Mongelli, Lidia Sarro, Elena Rizzo, et al.
Journal of the Neurological Sciences|May 1, 2019
Neuropsychological features of adult form of Alexander diseaseLara Draghi, Ettore Salsano, Laura Farina, et al.
Journal of Forensic Sciences|August 8, 2015
A Practical Guide for the Formulation of Propositions in the Bayesian Approach to DNA Evidence Interpretation in an Adversarial EnvironmentSimone Gittelson, Tim Kalafut, Steven Myers, et al.
Journal of Neuromuscular Diseases|May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literatureElena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.
Frontiers in Genetics|December 27, 2016
Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent ConcernsAlex Biedermann, Christophe Champod, Graham Jackson, et al.
Journal of Neurochemistry|March 16, 2026
Neurotrophic Modulation Restores Motor and Developmental Defects in Zebrafish Models of ints11 DeficiencyAnna Pistocchi, Elena Chiricozzi, Matilde Molteni, et al.
Experimental Neurology|March 18, 2009
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interferenceMaria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, et al.
Pageof 21