Vetri L - Search Results

1

EEG Patterns in Patients with Prader-Willi Syndrome.

Elia M, Rutigliano I, Sacco M, Madeo SF, Wasniewska M, Li Pomi A, Trifirò G, Di Bella P, De Lucia S, Vetri L, Iughetti L, Delvecchio M. Elia M, et al. Among authors: vetri l. Brain Sci. 2021 Aug 6;11(8):1045. doi: 10.3390/brainsci11081045. Brain Sci. 2021. PMID: 34439664 Free PMC article.

2

A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy.

Vetri L, Calì F, Vinci M, Amato C, Roccella M, Granata T, Freri E, Solazzi R, Romano V, Elia M. Vetri L, et al. Eur J Med Genet. 2020 Apr;63(4):103848. doi: 10.1016/j.ejmg.2020.103848. Epub 2020 Jan 20. Eur J Med Genet. 2020. PMID: 31972370

3

Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report.

Calì F, Elia M, Vinci M, Vetri L, Correnti E, Trapolino E, Roccella M, Vanadia F, Romano V. Calì F, et al. Among authors: vetri l. Medicina (Kaunas). 2020 Aug 1;56(8):387. doi: 10.3390/medicina56080387. Medicina (Kaunas). 2020. PMID: 32752300 Free PMC article.

4

Autism and Migraine: An Unexplored Association?

Vetri L. Vetri L. Brain Sci. 2020 Sep 6;10(9):615. doi: 10.3390/brainsci10090615. Brain Sci. 2020. PMID: 32899972 Free PMC article. Review.

5

Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".

Vetri L, Calì F, Vinci M, Amato C, Roccella M, Granata T, Freri E, Solazzi R, Romano V, Elia M. Vetri L, et al. Neuropediatrics. 2021 Apr;52(2):153. doi: 10.1055/s-0040-1716904. Epub 2020 Oct 27. Neuropediatrics. 2021. PMID: 33111300 No abstract available.

6

Impact of daytime routine modifications on people with severe intellectual disability amid COVID-19 pandemic.

Vetri L, Elia M, Vitello GA, Greco D, Gagliano C, Costanzo MC, Romeo G, Musumeci SA. Vetri L, et al. Perspect Psychiatr Care. 2021 Jul;57(3):1536-1537. doi: 10.1111/ppc.12696. Epub 2021 May 25. Perspect Psychiatr Care. 2021. PMID: 34032288 Free PMC article. No abstract available.

7

Prader-Willi Syndrome with Angelman Syndrome in the Offspring.

Greco D, Vetri L, Ragusa L, Vinci M, Gloria A, Occhipinti P, Costanzo AA, Quatrosi G, Roccella M, Buono S, Romano C. Greco D, et al. Among authors: vetri l. Medicina (Kaunas). 2021 May 8;57(5):460. doi: 10.3390/medicina57050460. Medicina (Kaunas). 2021. PMID: 34066798 Free PMC article.

8

Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 gene.

Vinci M, Kursula P, Greco D, Elia M, Vetri L, Schepis C, Chiavetta V, Donadio S, Roccella M, Carotenuto M, Romano V, Calì F. Vinci M, et al. Among authors: vetri l. Mol Genet Genomic Med. 2022 Sep;10(9):e2012. doi: 10.1002/mgg3.2012. Epub 2022 Jul 5. Mol Genet Genomic Med. 2022. PMID: 35789128 Free PMC article.

9

Epilepsy: A Multifaced Spectrum Disorder.

Vetri L, Roccella M, Parisi L, Smirni D, Costanza C, Carotenuto M, Elia M. Vetri L, et al. Behav Sci (Basel). 2023 Jan 23;13(2):97. doi: 10.3390/bs13020097. Behav Sci (Basel). 2023. PMID: 36829326 Free PMC article.

10

Poor School Academic Performance and Benign Epilepsy with Centro-Temporal Spikes.

Vetri L, Pepi A, Alesi M, Maltese A, Scifo L, Roccella M, Quatrosi G, Elia M. Vetri L, et al. Behav Sci (Basel). 2023 Jan 28;13(2):106. doi: 10.3390/bs13020106. Behav Sci (Basel). 2023. PMID: 36829335 Free PMC article. Review.

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