| Year |
Citation |
Score |
| 2024 |
Baginska U, Balagura G, Toonen RF, Verhage M. High-throughput assay for regulated secretion of neuropeptides in mouse and human neurons. The Journal of Biological Chemistry. 107321. PMID 38677517 DOI: 10.1016/j.jbc.2024.107321 |
0.402 |
|
| 2024 |
Iacomino M, Houerbi N, Fortuna S, Howe J, Li S, Scorrano G, Riva A, Cheng KW, Steiman M, Peltekova I, Yusuf A, Baldassari S, Tamburro S, Scudieri P, Musante I, ... ... Balagura G, et al. Allelic heterogeneity and abnormal vesicle recycling in -related neurodevelopmental disorders. Frontiers in Molecular Neuroscience. 17: 1268013. PMID 38650658 DOI: 10.3389/fnmol.2024.1268013 |
0.301 |
|
| 2022 |
Stamberger H, Crosiers D, Balagura G, Bonardi CM, Basu A, Cantalupo G, Chiesa V, Christensen J, Dalla Bernardina B, Ellis CA, Furia F, Gardiner F, Giron C, Guerrini R, Klein KM, et al. Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood. Neurology. 99: e221-e233. PMID 35851549 DOI: 10.1212/WNL.0000000000200715 |
0.365 |
|
| 2022 |
Balagura G, Xian J, Riva A, Marchese F, Ben Zeev B, Rios L, Sirsi D, Accorsi P, Amadori E, Astrea G, Baldassari S, Beccaria F, Boni A, Budetta M, Cantalupo G, et al. Epilepsy Course and Developmental Trajectories in -DEE. Neurology. Genetics. 8: e676. PMID 35655584 DOI: 10.1212/NXG.0000000000000676 |
0.451 |
|
| 2022 |
Scala M, Drouot N, MacLennan SC, Wessels MW, Krygier M, Pavinato L, Telegrafi A, de Man SA, van Slegtenhorst M, Iacomino M, Madia F, Scudieri P, Uva P, Giacomini T, Nobile G, ... ... Balagura G, et al. De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes. Human Mutation. PMID 35607920 DOI: 10.1002/humu.24414 |
0.337 |
|
| 2022 |
Accogli A, Lu S, Musante I, Scudieri P, Rosenfeld JA, Severino M, Baldassari S, Iacomino M, Riva A, Balagura G, Piccolo G, Minetti C, Roberto D, Xia F, Razak R, et al. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development. Cerebellum (London, England). PMID 35218524 DOI: 10.1007/s12311-022-01379-3 |
0.339 |
|
| 2021 |
Xian J, Parthasarathy S, Ruggiero SM, Balagura G, Fitch E, Helbig K, Gan J, Ganesan S, Kaufman MC, Ellis CA, Lewis-Smith D, Galer P, Cunningham K, O'Brien M, Cosico M, et al. Assessing the landscape of STXBP1-related disorders in 534 individuals. Brain : a Journal of Neurology. PMID 35190816 DOI: 10.1093/brain/awab327 |
0.478 |
|
| 2021 |
Houtman SJ, Lammertse HCA, van Berkel AA, Balagura G, Gardella E, Ramautar JR, Reale C, Møller RS, Zara F, Striano P, Misra-Isrie M, van Haelst MM, Engelen M, van Zuijen TL, Mansvelder HD, et al. Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG. Frontiers in Physiology. 12: 775172. PMID 35002760 DOI: 10.3389/fphys.2021.775172 |
0.461 |
|
| 2021 |
Riva A, Golda A, Balagura G, Amadori E, Vari MS, Piccolo G, Iacomino M, Lattanzi S, Salpietro V, Minetti C, Striano P. New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment. Frontiers in Neurology. 12: 753753. PMID 34950099 DOI: 10.3389/fneur.2021.753753 |
0.308 |
|
| 2021 |
Lewis-Smith D, Galer PD, Balagura G, Kearney H, Ganesan S, Cosico M, O'Brien M, Vaidiswaran P, Krause R, Ellis CA, Thomas RH, Robinson PN, Helbig I. Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable. Epilepsia. PMID 33949685 DOI: 10.1111/epi.16908 |
0.3 |
|
| 2021 |
Riva A, Coppola A, Balagura G, Scala M, Iacomino M, Marchese F, Amadori E, Lattanzi S, Meo R, Striano S, Salpietro V, Zara F, Minetti C, Striano P, Bilo L. Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation. Epileptic Disorders : International Epilepsy Journal With Videotape. 23: 397-401. PMID 33851920 DOI: 10.1684/epd.2021.1266 |
0.345 |
|
| 2020 |
Balagura G, Cacciatore M, Grasso EA, Striano P, Verrotti A. Fenfluramine for the Treatment of Dravet Syndrome and Lennox-Gastaut Syndrome. Cns Drugs. 34: 1001-1007. PMID 32875491 DOI: 10.1007/s40263-020-00755-z |
0.3 |
|
| 2020 |
Balagura G, Riva A, Marchese F, Iacomino M, Madia F, Giacomini T, Mancardi MM, Amadori E, Vari MS, Salpietro V, Russo A, Messana T, Vignoli A, Chiesa V, Giordano L, et al. Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. PMID 32651081 DOI: 10.1016/J.Ejpn.2020.06.005 |
0.437 |
|
| 2018 |
Brigo F, Striano P, Balagura G, Belcastro V. Emerging drugs for the treatment of Dravet syndrome. Expert Opinion On Emerging Drugs. 23: 261-269. PMID 30482063 DOI: 10.1080/14728214.2018.1552937 |
0.314 |
|
| Show low-probability matches. |