Concepedia

Author

Veronica Saletti

Fondazione IRCCS Istituto Neurologico Carlo BestaORCID

Also Known As

Chiara Pantaleoni, De Luca, Alessandro, Federica Zibordi, Francesca Ragona, SALETTI, VERONICA, Saletti Veronica, Saletti, Veronica, V. Saletti, Veronica Saletti, Walsh, Laurence E.

94

Publications

2.8K

Citations

25

H-Index

104

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo BestaUniversity of MilanIstituti di Ricovero e Cura a Carattere ScientificoFondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoBambino Gesù Children's Hospital
VS

About

Veronica Saletti is an author at Fondazione IRCCS Istituto Neurologico Carlo Besta specializing in medicine, neurology, and neuropathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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Health Sciences

2

2

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3

Language Studies

2

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Natural Sciences

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Public Health

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Veronica Saletti

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46

Publications

2.6K

Citations

25

H-Index

YearCitations

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens,

Nature Genetics

2014

311

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848

Magdalena Koczkowska, Yunjia Chen, Tom Callens,

The American Journal of Human Genetics

2017

203

The molecular landscape of glioma in patients with Neurofibromatosis 1

Fulvio D’Angelo, Michele Ceccarelli, Tala,

Nature Medicine

2018

203

Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy

Jennifer Friedman, Emmanuel Roze, José E. Abdenur,

Annals of Neurology

2011

154

Clinical spectrum of individuals with pathogenic <i> <b>N</b> F1 </i> missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

Magdalena Koczkowska, Tom Callens, Yunjia Chen,

Human Mutation

2019

130

Diagnosis and treatment of Chiari malformation and syringomyelia in adults: international consensus document

P. Ciaramitaro, Luca Massimi, Alessandro Bertuccio,

Neurological Sciences

2021

120

Intrathecal methotrexate affects cognitive function in children with medulloblastoma

Daria Riva, C. Giorgi, Francesca Nichelli,

Neurology

2002

115

Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function

Gillian Rice, Sehoon Park, Francesco Gavazzi,

Human Mutation

2020

107

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation

Magdalena Koczkowska, Tom Callens, Alicia Gomes,

Genetics in Medicine

2018

93

Late neuropsychological and behavioural outcome of children surgically treated for craniopharyngioma

Daria Riva, Chiara Pantaleoni, Monica Devoti,

Child s Nervous System

1998

85

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