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Veronica Saletti

Showing results (41-50 of 70) with videos related to

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Genes|June 25, 2020
Simultaneous Detection of <i>NF1</i>, <i>SPRED1</i>, <i>LZTR1</i>, and <i>NF2</i> Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 PatientsDonatella Bianchessi, Maria Cristina Ibba, Veronica Saletti, et al.
Journal of Human Genetics|February 27, 2018
Correction: The absence that makes the difference: choroidal abnormalities in Legius syndromeArianna Tucci, Veronica Saletti, Francesca Menni, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 27, 2026
Pharmacokinetics and Safety of Selumetinib Granule Formulation in Children With Symptomatic, Inoperable Neurofibromatosis Type 1-Related Plexiform Neurofibromas (SPRINKLE; phase I/II)Pablo Hernáiz Driever, Uwe R Kordes, Ines B Brecht, et al.
European Journal of Human Genetics : EJHG|May 22, 2023
New insights into the molecular basis of spinal neurofibromatosis type 1Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, et al.
Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
International Journal of Molecular Sciences|January 21, 2023
Increase of Circulating Endothelial Progenitor Cells and Released Angiogenic Factors in Children with Moyamoya ArteriopathyGemma Gorla, Tatiana Carrozzini, Giuliana Pollaci, et al.
Cancers|November 27, 2019
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent CohortGiulia Melloni, Marica Eoli, Claudia Cesaretti, et al.
Cancers|January 8, 2023
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian CohortRosina Paterra, Paola Bettinaglio, Arianna Borghi, et al.
Research in Developmental Disabilities|June 13, 2024
Quality of life, functioning and participation of children and adolescents with visual impairment: A scoping reviewMartina Lanza, Francesca Incagli, Chiara Ceccato, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 15, 2018
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disordersAmbra Rizzo, Enrico Alfei, Federica Zibordi, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Genes|June 25, 2020
Simultaneous Detection of <i>NF1</i>, <i>SPRED1</i>, <i>LZTR1</i>, and <i>NF2</i> Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 PatientsDonatella Bianchessi, Maria Cristina Ibba, Veronica Saletti, et al.
Journal of Human Genetics|February 27, 2018
Correction: The absence that makes the difference: choroidal abnormalities in Legius syndromeArianna Tucci, Veronica Saletti, Francesca Menni, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 27, 2026
Pharmacokinetics and Safety of Selumetinib Granule Formulation in Children With Symptomatic, Inoperable Neurofibromatosis Type 1-Related Plexiform Neurofibromas (SPRINKLE; phase I/II)Pablo Hernáiz Driever, Uwe R Kordes, Ines B Brecht, et al.
European Journal of Human Genetics : EJHG|May 22, 2023
New insights into the molecular basis of spinal neurofibromatosis type 1Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, et al.
Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
International Journal of Molecular Sciences|January 21, 2023
Increase of Circulating Endothelial Progenitor Cells and Released Angiogenic Factors in Children with Moyamoya ArteriopathyGemma Gorla, Tatiana Carrozzini, Giuliana Pollaci, et al.
Cancers|November 27, 2019
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent CohortGiulia Melloni, Marica Eoli, Claudia Cesaretti, et al.
Cancers|January 8, 2023
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian CohortRosina Paterra, Paola Bettinaglio, Arianna Borghi, et al.
Research in Developmental Disabilities|June 13, 2024
Quality of life, functioning and participation of children and adolescents with visual impairment: A scoping reviewMartina Lanza, Francesca Incagli, Chiara Ceccato, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 15, 2018
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disordersAmbra Rizzo, Enrico Alfei, Federica Zibordi, et al.
Pageof 7