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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 10
2003 7
2004 14
2005 4
2006 12
2007 10
2008 15
2009 19
2010 26
2011 29
2012 24
2013 30
2014 38
2015 27
2016 28
2017 30
2018 27
2019 28
2020 31
2021 32
2022 30
2023 14
2024 20
2025 14
2026 3

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453 results

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Page 1
Meconium aspiration syndrome: from pathophysiology to treatment.
Dini G, Ceccarelli S, Celi F, Semeraro CM, Gorello P, Verrotti A. Dini G, et al. Among authors: verrotti a. Ann Med Surg (Lond). 2024 Feb 15;86(4):2023-2031. doi: 10.1097/MS9.0000000000001835. eCollection 2024 Apr. Ann Med Surg (Lond). 2024. PMID: 38576961 Free PMC article. Review.
Temporal Lobe Epilepsy and Psychiatric Comorbidity.
Vinti V, Dell'Isola GB, Tascini G, Mencaroni E, Cara GD, Striano P, Verrotti A. Vinti V, et al. Among authors: verrotti a. Front Neurol. 2021 Nov 30;12:775781. doi: 10.3389/fneur.2021.775781. eCollection 2021. Front Neurol. 2021. PMID: 34917019 Free PMC article. Review.
Cyclic Vomiting Syndrome in Children.
Raucci U, Borrelli O, Di Nardo G, Tambucci R, Pavone P, Salvatore S, Baldassarre ME, Cordelli DM, Falsaperla R, Felici E, Ferilli MAN, Grosso S, Mallardo S, Martinelli D, Quitadamo P, Pensabene L, Romano C, Savasta S, Spalice A, Strisciuglio C, Suppiej A, Valeriani M, Zenzeri L, Verrotti A, Staiano A, Villa MP, Ruggieri M, Striano P, Parisi P. Raucci U, et al. Among authors: verrotti a. Front Neurol. 2020 Nov 2;11:583425. doi: 10.3389/fneur.2020.583425. eCollection 2020. Front Neurol. 2020. PMID: 33224097 Free PMC article.
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, Procaccio V, Striano P, Mankad K, Lieb A, Chen S, Pisani L, Bettencourt C, Männikkö R, Manole A, Brusco A, Grosso E, Ferrero GB, Armstrong-Moron J, Gueden S, Bar-Yosef O, Tzadok M, Monaghan KG, Santiago-Sim T, Person RE, Cho MT, Willaert R, Yoo Y, Chae JH, Quan Y, Wu H, Wang T, Bernier RA, Xia K, Blesson A, Jain M, Motazacker MM, Jaeger B, Schneider AL, Boysen K, Muir AM, Myers CT, Gavrilova RH, Gunderson L, Schultz-Rogers L, Klee EW, Dyment D, Osmond M, Parellada M, Llorente C, Gonzalez-Peñas J, Carracedo A, Van Haeringen A, Ruivenkamp C, Nava C, Heron D, Nardello R, Iacomino M, Minetti C, Skabar A, Fabretto A; SYNAPS Study Group; Raspall-Chaure M, Chez M, Tsai A, Fassi E, Shinawi M, Constantino JN, De Zorzi R, Fortuna S, Kok F, Keren B, Bonneau D, Choi M, Benzeev B, Zara F, Mefford HC, Scheffer IE, Clayton-Smith J, Macaya A, Rothman JE, Eichler EE, Kullmann DM, Houlden H. Salpietro V, et al. Nat Commun. 2019 Jul 12;10(1):3094. doi: 10.1038/s41467-019-10910-w. Nat Commun. 2019. PMID: 31300657 Free PMC article.
Developmental coordination disorder and epilepsy.
Esposito M, Santomauro R, Dell'Isola GB, Ruberto M, Verrotti A, Siciliano M, Carotenuto M. Esposito M, et al. Among authors: verrotti a. World J Pediatr. 2025 Jan;21(1):1-2. doi: 10.1007/s12519-024-00869-0. Epub 2024 Dec 21. World J Pediatr. 2025. PMID: 39707046 No abstract available.
Valproate-induced hyperammonemic encephalopathy.
Verrotti A, Trotta D, Morgese G, Chiarelli F. Verrotti A, et al. Metab Brain Dis. 2002 Dec;17(4):367-73. doi: 10.1023/a:1021918104127. Metab Brain Dis. 2002. PMID: 12602513 Review.
SLK is mutated in individuals with a neurodevelopmental disorder.
Alabdi L, Altuwaijri N, Zhu JY, Efthymiou S, Lee H, Duan J, Salem I, Yu P, Abdullah NL, Alzahrani F, Xu Q, Felemban MM, Alfaifi A, Rahman F, Christoforou M, Maqbool S, Martinez-Agosto JA, Alsaif HS, Hashem M, Helaby R, Alsulaiman A; SYNaPS Study Group; Queen Square Genomics; Maroofian R, Houlden H, Arold ST, Ibrahim LA, Han Z, Alkuraya FS. Alabdi L, et al. EBioMedicine. 2025 Jun;116:105725. doi: 10.1016/j.ebiom.2025.105725. Epub 2025 May 9. EBioMedicine. 2025. PMID: 40347834 Free PMC article.
Current Overview of CDKL-5 Deficiency Disorder Treatment.
Dell'Isola GB, Portwood KE, Consing K, Fattorusso A, Bartocci A, Ferrara P, Di Cara G, Verrotti A, Lodolo M. Dell'Isola GB, et al. Among authors: verrotti a. Pediatr Rep. 2024 Jan 3;16(1):21-25. doi: 10.3390/pediatric16010002. Pediatr Rep. 2024. PMID: 38251311 Free PMC article.
453 results