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Veronica Saletti

Showing results (31-40 of 70) with videos related to

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European Journal of Medical Genetics|December 12, 2018
Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experienceClaudia Ciaccio, Veronica Saletti, Stefano D'Arrigo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2010
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-upBruna Molteni, Daniela Sarti, Gloria Airaghi, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
126 novel mutations in Italian patients with neurofibromatosis type 1Donatella Bianchessi, Sara Morosini, Veronica Saletti, et al.
Journal of Autism and Developmental Disorders|January 4, 2021
CGH Findings in Children with Complex and Essential Autistic Spectrum DisorderSilvia Annunziata, Sara Bulgheroni, Stefano D'Arrigo, et al.
Journal of Child Neurology|May 7, 2015
Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and PeculiaritiesSimona Binelli, Francesca Ragona, Laura Canafoglia, et al.
Diagnostics (Basel, Switzerland)|May 13, 2023
Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center ExperienceMatilde Taddei, Silvia Esposito, Gianluca Marucci, et al.
International Journal of Molecular Sciences|January 11, 2022
The Lipid Asset Is Unbalanced in Peripheral Nerve Sheath TumorsIgnazio G Vetrano, Michele Dei Cas, Vittoria Nazzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2017
A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuationsSilvia Esposito, Miryam Carecchio, Davide Tonduti, et al.
Journal of Human Genetics|July 28, 2017
The absence that makes the difference: choroidal abnormalities in Legius syndromeArianna Tucci, Veronica Saletti, Francesca Menni, et al.
Human Genetics|June 14, 2024
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genesViviana Tritto, Paola Bettinaglio, Eleonora Mangano, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
European Journal of Medical Genetics|December 12, 2018
Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experienceClaudia Ciaccio, Veronica Saletti, Stefano D'Arrigo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2010
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-upBruna Molteni, Daniela Sarti, Gloria Airaghi, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
126 novel mutations in Italian patients with neurofibromatosis type 1Donatella Bianchessi, Sara Morosini, Veronica Saletti, et al.
Journal of Autism and Developmental Disorders|January 4, 2021
CGH Findings in Children with Complex and Essential Autistic Spectrum DisorderSilvia Annunziata, Sara Bulgheroni, Stefano D'Arrigo, et al.
Journal of Child Neurology|May 7, 2015
Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and PeculiaritiesSimona Binelli, Francesca Ragona, Laura Canafoglia, et al.
Diagnostics (Basel, Switzerland)|May 13, 2023
Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center ExperienceMatilde Taddei, Silvia Esposito, Gianluca Marucci, et al.
International Journal of Molecular Sciences|January 11, 2022
The Lipid Asset Is Unbalanced in Peripheral Nerve Sheath TumorsIgnazio G Vetrano, Michele Dei Cas, Vittoria Nazzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2017
A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuationsSilvia Esposito, Miryam Carecchio, Davide Tonduti, et al.
Journal of Human Genetics|July 28, 2017
The absence that makes the difference: choroidal abnormalities in Legius syndromeArianna Tucci, Veronica Saletti, Francesca Menni, et al.
Human Genetics|June 14, 2024
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genesViviana Tritto, Paola Bettinaglio, Eleonora Mangano, et al.
Pageof 7