Cetica V - Search Results

1

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene.

Barba C, Blumcke I, Winawer MR, Hartlieb T, Kang HC, Grisotto L, Chipaux M, Bien CG, Heřmanovská B, Porter BE, Lidov HGW, Cetica V, Woermann FG, Lopez-Rivera JA, Canoll PD, Mader I, D'Incerti L, Baldassari S, Yang E, Gaballa A, Vogel H, Straka B, Macconi L, Polster T, Grant GA, Krsková L, Shin HJ, Ko A, Crino PB, Krsek P, Lee JH, Lal D, Baulac S, Poduri A, Guerrini R; SLC35A2 Study Group. Barba C, et al. Among authors: cetica v. Neurology. 2023 Jan 31;100(5):e528-e542. doi: 10.1212/WNL.0000000000201471. Epub 2022 Oct 28. Neurology. 2023. PMID: 36307217 Free PMC article.

2

Myxoid glioneuronal tumor: Histopathologic, neuroradiologic, and molecular features in a single center series.

Caporalini C, Scagnet M, Giunti L, Cetica V, Mei D, Conti V, Moscardi S, Macconi L, Giordano F, D'Incerti L, Genitori L, Guerrini R, Buccoliero AM. Caporalini C, et al. Among authors: cetica v. Neoplasia. 2023 Mar;37:100885. doi: 10.1016/j.neo.2023.100885. Epub 2023 Feb 8. Neoplasia. 2023. PMID: 36764090 Free PMC article.

3

Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants.

Panza N, Bianchini C, Cetica V, Balestrini S, Barba C, Ferrari AR, Mei D, Parmeggiani L, Parrini E, Guerrini R. Panza N, et al. Among authors: cetica v. Epilepsia Open. 2024 Feb;9(1):417-423. doi: 10.1002/epi4.12843. Epub 2023 Dec 15. Epilepsia Open. 2024. PMID: 37805811 Free PMC article.

4

Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase.

Buccoliero AM, Caporalini C, Moscardi S, Cetica V, Mei D, Conti V, Nozzoli F, Bonaudo C, Battista F, Giordano F, Mura R, Spacca B, Mussa F, D'Onofrio V, Guerrini R, Genitori L, Scagnet M. Buccoliero AM, et al. Among authors: cetica v. Epilepsy Res. 2024 Jan;199:107258. doi: 10.1016/j.eplepsyres.2023.107258. Epub 2023 Nov 21. Epilepsy Res. 2024. PMID: 38086219

5

Clinical and molecular characterization of patients with YWHAG-related epilepsy.

Cetica V, Pisano T, Lesca G, Marafi D, Licchetta L, Riccardi F, Mei D, Chung HB, Bayat A, Balasubramanian M, Lowenstein DH, Endzinienė M, Alotaibi M, Villeneuve N, Jacobs J, Isidor B, Solazzi R, den Hollander NS, Marjanovic D, Rougeot-Jung C, Jung J, Lesieur-Sebellin M, Accogli A, Salpietro V, Saadi NW, Panagiotakaki E, Foiadelli T, Redon S, Tsai MH, Bisulli F, Hammer TB, Lupski JR, Parrini E, Guerrini R; YWHAG Study Group. Cetica V, et al. Epilepsia. 2024 May;65(5):1439-1450. doi: 10.1111/epi.17939. Epub 2024 Mar 16. Epilepsia. 2024. PMID: 38491959

6

Confirmation of the Pathogenetic Role of the CCDC88C Gene in Early-Onset Pure Spastic Paraplegia.

Caputo D, Cetica V, Paoli S, Rosati A, Lazzeri S. Caputo D, et al. Among authors: cetica v. Mov Disord. 2023 Aug;38(8):1561-1562. doi: 10.1002/mds.29459. Epub 2023 Jun 15. Mov Disord. 2023. PMID: 37317935 No abstract available.

7

Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous POMT2 Missense Mutations.

Zago S, Silvestri E, Arcangeli T, Calisesi M, Romeo C, Parmeggiani G, Parrini E, Cetica V, Guerrini R, Palicelli A, Bonasoni MP. Zago S, et al. Among authors: cetica v. Fetal Pediatr Pathol. 2023 Apr;42(2):334-341. doi: 10.1080/15513815.2022.2116620. Epub 2022 Sep 1. Fetal Pediatr Pathol. 2023. PMID: 36048137

8

STOP Pain Project-Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways.

Crescioli G, Lombardi N, Vagnoli L, Bettiol A, Giunti L, Cetica V, Coniglio ML, Provenzano A, Giglio S, Bonaiuti R, Mugelli A, Aricò M, Messeri A, Vannacci A, Maggini V. Crescioli G, et al. Among authors: cetica v. Pharmaceutics. 2022 Mar 11;14(3):619. doi: 10.3390/pharmaceutics14030619. Pharmaceutics. 2022. PMID: 35335997 Free PMC article.

9

Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.

Mei D, Cetica V, Marini C, Guerrini R. Mei D, et al. Among authors: cetica v. Epilepsia. 2019 Dec;60 Suppl 3:S2-S7. doi: 10.1111/epi.16054. Epilepsia. 2019. PMID: 31904125 Review.

10

A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data.

Laccetta G, Fiori S, Giampietri M, Ferrari A, Cetica V, Bernardini M, Chesi F, Mazzotti S, Parrini E, Ciantelli M, Guzzetta A, Ghirri P. Laccetta G, et al. Among authors: cetica v. Front Pediatr. 2019 Sep 6;7:348. doi: 10.3389/fped.2019.00348. eCollection 2019. Front Pediatr. 2019. PMID: 31552204 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

39 results

Search Page