Veronica Saletti

Veronica Saletti

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Veronica Saletti

Veronica Saletti

Publications by authors named "Veronica Saletti"

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Neurological malignancies in neurofibromatosis type 1.

Curr Opin Oncol 2019 Nov;31(6):554-561

Molecular Neuro-Oncology Unit.

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http://dx.doi.org/10.1097/CCO.0000000000000576DOI Listing
November 2019

Chiari 1 malformation and untreated sagittal synostosis: a new subset of complex Chiari?

Childs Nerv Syst 2019 Oct 21;35(10):1741-1753. Epub 2019 Jul 21.

Neurosurgery Department, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s00381-019-04283-0DOI Listing
October 2019

Chiari I malformation in defined genetic syndromes in children: are there common pathways?

Childs Nerv Syst 2019 Oct 30;35(10):1727-1739. Epub 2019 Jul 30.

Department of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1007/s00381-019-04319-5DOI Listing
October 2019

Fluorescein-guided resection of plexiform neurofibromas: how I do it.

Acta Neurochir (Wien) 2019 Oct 21;161(10):2141-2145. Epub 2019 Aug 21.

Neurosurgery Unit III, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1007/s00701-019-04038-5DOI Listing
October 2019

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276 and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1.

Authors:
Magdalena Koczkowska Tom Callens Yunjia Chen Alicia Gomes Alesha D Hicks Angela Sharp Eric Johns Kim Armfield Uhas Linlea Armstrong Katherine Armstrong Bosanko Dusica Babovic-Vuksanovic Laura Baker Donald G Basel Mario Bengala James T Bennett Chelsea Chambers Lola K Clarkson Maurizio Clementi Fanny M Cortés Mitch Cunningham M Daniela D'Agostino Martin B Delatycki Maria C Digilio Laura Dosa Silvia Esposito Stephanie Fox Mary-Louise Freckmann Christine Fauth Teresa Giugliano Sandra Giustini Allison Goetsch Yael Goldberg Robert S Greenwood Cristin Griffis Karen W Gripp Punita Gupta Eric Haan Rachel K Hachen Tamara L Haygarth Concepción Hernández-Chico Katelyn Hodge Robert J Hopkin Louanne Hudgins Sandra Janssens Kory Keller Geraldine Kelly-Mancuso Aaina Kochhar Bruce R Korf Andrea M Lewis Jan Liebelt Angie Lichty Robert H Listernick Michael J Lyons Isabelle Maystadt Mayra Martinez Ojeda Carey McDougall Lesley K McGregor Daniela Melis Nancy Mendelsohn Malgorzata J M Nowaczyk June Ortenberg Karin Panzer John G Pappas Mary Ella Pierpont Giulio Piluso Valentina Pinna Eniko K Pivnick Dinel A Pond Cynthia M Powell Caleb Rogers Noa Ruhrman Shahar S Lane Rutledge Veronica Saletti Sarah A Sandaradura Claudia Santoro Ulrich A Schatz Allison Schreiber Daryl A Scott Elizabeth A Sellars Ruth Sheffer Elizabeth Siqveland John M Slopis Rosemarie Smith Alberto Spalice David W Stockton Haley Streff Amy Theos Gail E Tomlinson Grace Tran Pamela L Trapane Eva Trevisson Nicole J Ullrich Jenneke Van den Ende Samantha A Schrier Vergano Stephanie E Wallace Michael F Wangler David D Weaver Kaleb H Yohay Elaine Zackai Jonathan Zonana Vickie Zurcher Kathleen B M Claes Marica Eoli Yolanda Martin Katharina Wimmer Alessandro De Luca Eric Legius Ludwine M Messiaen

Hum Mutat 2019 Oct 8. Epub 2019 Oct 8.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

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http://dx.doi.org/10.1002/humu.23929DOI Listing
October 2019

Visuoperceptual Impairment in Children with NF1: From Early Visual Processing to Procedural Strategies.

Behav Neurol 2019 13;2019:7146168. Epub 2019 Jan 13.

Developmental Neurology Division, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.

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http://dx.doi.org/10.1155/2019/7146168DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348799PMC
July 2019

Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency.

Metab Brain Dis 2019 Jul 22. Epub 2019 Jul 22.

Pediatric Neurology Unit, V. Buzzi Children's Hospital, Via Castelvetro 32, 20154, Milan, Italy.

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http://dx.doi.org/10.1007/s11011-019-00464-7DOI Listing
July 2019

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.

Genet Med 2019 04 7;21(4):867-876. Epub 2018 Sep 7.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://dx.doi.org/10.1038/s41436-018-0269-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752285PMC
April 2019

Correction: 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.

Genet Med 2019 03;21(3):764-765

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.

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http://www.nature.com/articles/s41436-018-0326-8
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http://dx.doi.org/10.1038/s41436-018-0326-8DOI Listing
March 2019

Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience.

Eur J Med Genet 2018 Dec 4. Epub 2018 Dec 4.

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212183042
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http://dx.doi.org/10.1016/j.ejmg.2018.12.001DOI Listing
December 2018

Unique combination of myxopapillary ependymoma and conus lipoma with subcutaneous extension in an 11-month-old child.

Childs Nerv Syst 2018 04 29;34(4):597-599. Epub 2018 Jan 29.

Department of Neurosurgery, Fondazione IRCCS "Istituto Neurologico C. Besta", Via G. Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s00381-018-3738-5DOI Listing
April 2018

Correction: The absence that makes the difference: choroidal abnormalities in Legius syndrome.

J Hum Genet 2018 03 7;63(3):391. Epub 2018 Feb 7.

Medical Genetics Unit Woman, Child and Newborn department, IRCSS Foundation, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1038/s10038-017-0369-8DOI Listing
March 2018

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

Am J Hum Genet 2018 01 28;102(1):69-87. Epub 2017 Dec 28.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.12.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777934PMC
January 2018

The absence that makes the difference: choroidal abnormalities in Legius syndrome.

J Hum Genet 2017 Nov 27;62(11):1001-1004. Epub 2017 Jul 27.

Medical Genetics Unit Woman, Child and Newborn department, IRCSS Foundation, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1038/jhg.2017.78DOI Listing
November 2017

A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.

Mov Disord 2017 11 26;32(11):1646-1647. Epub 2017 Sep 26.

Department of Neurology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.

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http://dx.doi.org/10.1002/mds.27175DOI Listing
November 2017

Chiari I malformation in a child with PTEN hamartoma tumor syndrome: Association or coincidence?

Eur J Med Genet 2017 May 7;60(5):261-264. Epub 2017 Mar 7.

Neuroradiology Department, Foundation IRCCS Neurological Institute Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1016/j.ejmg.2017.03.002DOI Listing
May 2017

Legius Syndrome: two novel mutations in the SPRED1 gene.

Hum Genome Var 2015 3;2:15051. Epub 2015 Dec 3.

Laboratory of Experimental Neurobiology, 'C. Mondino' National Neurological Institute , Pavia, Italy.

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http://dx.doi.org/10.1038/hgv.2015.51DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785569PMC
April 2016

Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and Peculiarities.

J Child Neurol 2015 Nov 5;30(13):1824-30. Epub 2015 May 5.

Department of Neurophysiopathology, Epilepsy Centre, C. Besta Foundation Neurological Institute, Milan, Italy

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http://dx.doi.org/10.1177/0883073815583687DOI Listing
November 2015

Response to "Characteristics of 2p15-p16.1 microdeletion syndrome: review and description of two additional patients".

Congenit Anom (Kyoto) 2015 Nov;55(4):191-2

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy.

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http://dx.doi.org/10.1111/cga.12119DOI Listing
November 2015

126 novel mutations in Italian patients with neurofibromatosis type 1.

Mol Genet Genomic Med 2015 Nov 7;3(6):513-25. Epub 2015 Jul 7.

Molecular Neuro-oncology IRCCS Foundation, "C. Besta" Neurological Institute Milan Italy.

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http://dx.doi.org/10.1002/mgg3.161DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694136PMC
November 2015

Neuroradiological diagnosis of Chiari malformations.

Neurol Sci 2011 Dec;32 Suppl 3:S283-6

Department of Neuroradiology, Foundation IRCCS Neurological Institute Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-011-0695-0DOI Listing
December 2011

Treatment for Chiari 1 malformation (CIM): analysis of a pediatric surgical series.

Neurol Sci 2011 Dec;32 Suppl 3:S321-4

Department of Neurosurgery, Fondazione Istituto Neurologico C. Besta, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-011-0731-0DOI Listing
December 2011

Neurological pictures in paediatric Chiari I malformation.

Neurol Sci 2011 Dec;32 Suppl 3:S295-8

UO Neurologia dello Sviluppo, Fondazione IRCCS Istituto Neurologico C. Besta, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-011-0744-8DOI Listing
December 2011

Can Chiari malformation negatively affect higher mental functioning in developmental age?

Neurol Sci 2011 Dec;32 Suppl 3:S307-9

UO Neurologia dello Sviluppo, Fondazione IRCCS Istituto Neurologico C. Besta, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-011-0779-xDOI Listing
December 2011

The neurophysiological balance in Chiari type 1 malformation (CM1), tethered cord and related syndromes.

Neurol Sci 2011 Dec;32 Suppl 3:S311-6

Fondazione IRCCS Istituto Nazionale Neurologico C.Besta, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-011-0692-3DOI Listing
December 2011

Paediatric Stroke: Review of the Literature and Possible Treatment Options, including Endovascular Approach.

Stroke Res Treat 2011 7;2011:781612. Epub 2011 Jul 7.

Neuroradiology Department, Fondazione Istituto "C. Besta", Via Celoria 11, 20133 Milan, Italy.

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http://dx.doi.org/10.4061/2011/781612DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140077PMC
November 2011

Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-up.

Neurol Sci 2010 Aug 2;31(4):471-81. Epub 2010 Jun 2.

Developmental Neurology Division, Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, via Celoria, 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-010-0309-2DOI Listing
August 2010

A CDKL5 mutated child with precocious puberty.

Am J Med Genet A 2009 May;149A(5):1046-51

Developmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.

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http://dx.doi.org/10.1002/ajmg.a.32806DOI Listing
May 2009

Verbal and gestural communication in children with bilateral perisylvian polymicrogyria.

J Child Neurol 2007 Sep;22(9):1090-8

Developmental Neurology Division, Istituto Nazionale Neurologico, Besta, Milano, Italy.

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http://dx.doi.org/10.1177/0883073807306247DOI Listing
September 2007

Neuropsychologic effects of frontal lobe epilepsy in children.

J Child Neurol 2002 Sep;17(9):661-7

Developmental Neurology Division, Istituto Nazionale Neurologico C. Besta, Milano, Italy.

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http://dx.doi.org/10.1177/088307380201700902DOI Listing
September 2002