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Carlo Minetti

Showing results (101-110 of 190) with videos related to

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Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Neurology. Genetics|August 18, 2017
Novel <i>AMPD2</i> mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalitiesAndrea Accogli, Michele Iacomino, Francesca Pinto, et al.
Epilepsy & Behavior : E&B|February 1, 2016
Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Carmela Caccavale, Lia Santulli, et al.
Epilepsia|March 2, 2013
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletionAntonietta Coppola, Irene Bagnasco, Monica Traverso, et al.
Human Mutation|December 6, 2013
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical developmentChiara Fiorillo, Francesca Moro, Julie Yi, et al.
Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Clinical Drug Investigation|October 29, 2015
Safety of Overnight Switch from Brand-Name to Generic LevetiracetamMaria Stella Vari, Francesca Pinto, Elisabetta Mencaroni, et al.
Biochemical and Biophysical Research Communications|February 18, 2006
A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmyDenise Cassandrini, Maria Grazia Calevo, Alessandra Tessa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2010
The spectrum of GNE mutations: allelic heterogeneity for a common phenotypeMarina Grandis, Rossella Gulli, Denise Cassandrini, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Pageof 19

Showing results (101-110 of 190) with videos related to

Sort By:
Pageof 19
Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Neurology. Genetics|August 18, 2017
Novel <i>AMPD2</i> mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalitiesAndrea Accogli, Michele Iacomino, Francesca Pinto, et al.
Epilepsy & Behavior : E&B|February 1, 2016
Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Carmela Caccavale, Lia Santulli, et al.
Epilepsia|March 2, 2013
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletionAntonietta Coppola, Irene Bagnasco, Monica Traverso, et al.
Human Mutation|December 6, 2013
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical developmentChiara Fiorillo, Francesca Moro, Julie Yi, et al.
Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Clinical Drug Investigation|October 29, 2015
Safety of Overnight Switch from Brand-Name to Generic LevetiracetamMaria Stella Vari, Francesca Pinto, Elisabetta Mencaroni, et al.
Biochemical and Biophysical Research Communications|February 18, 2006
A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmyDenise Cassandrini, Maria Grazia Calevo, Alessandra Tessa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2010
The spectrum of GNE mutations: allelic heterogeneity for a common phenotypeMarina Grandis, Rossella Gulli, Denise Cassandrini, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Pageof 19