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

Year Number of Results
1989 1
1992 1
1993 1
1994 1
1995 1
1996 6
1997 2
1998 6
1999 6
2000 9
2001 9
2002 8
2003 10
2004 13
2005 13
2006 15
2007 14
2008 21
2009 19
2010 21
2011 20
2012 11
2013 20
2014 21
2015 8
2016 12
2017 7
2018 17
2019 20
2020 20
2021 20
2022 17
2023 14
2024 15
2025 17

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370 results

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Page 1
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: grosso s. Front Neurol. 2020 Nov 2;11:583425. doi: 10.3389/fneur.2020.583425. eCollection 2020. Front Neurol. 2020. PMID: 33224097 Free PMC article.
Groove pancreatitis.
Valentini G, Surace M, Grosso S, Vernetto A, Serra AM, Andria I, Mazzucco D. Valentini G, et al. Among authors: grosso s. Minerva Gastroenterol (Torino). 2023 Sep;69(3):436-438. doi: 10.23736/S2724-5985.20.02721-X. Epub 2020 Jul 16. Minerva Gastroenterol (Torino). 2023. PMID: 32677417 No abstract available.
AUTS2-related syndrome: Insights from a large European cohort.
Loberti L, Adamo L, Antolini E, Casamassima G, Destrèe A, Brunetti-Pierri N, Genevieve D, Christophe P, Coubes C, Van Esch H, Herget T, Kortüm F, Lisfeld J, Möllring AC, Zenker M, Levy J, Perrin L, Tabet AC, Maruani A, Sorlin A, Stieber D, Herissant L, Dahan K, Sinibaldi L, Capolino R, Dentici ML, Dallapiccola B, Novelli A, Garavelli L, Caraffi SG, Piatelli G, Valenzuela I, Digilio MC, Caumes R, Knopp C, Chwiałkowska K, Jezela-Stanek A, Kwasniewski M, Korotko U, Gorzałczyńska E, Canitano R, Grosso S, Rahikkala E, Mattern L, Elbracht M, Zuffardi O, Caputo V, Toschi B, Beunders G, Leeuwen L, Elting MW, van der Laan L, Broekema MF, Groffen AJ, van de Kamp JM, van Haelst MM, Alders M, Mauro SP, De Razza F, Varvara D, Kick J, Gaspar H, Braun D, Lausberg E, Maier A, Ruault V, Genesio R, Tartaglia M, Tita R, Bruttini M, Longo I, Baldassarri M, Mencarelli MA, Renieri A, Pinto AM. Loberti L, et al. Among authors: grosso s. Genet Med. 2025 Jun;27(6):101375. doi: 10.1016/j.gim.2025.101375. Epub 2025 Feb 12. Genet Med. 2025. PMID: 39953909 Free article.
The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II).
Parenti G, Fecarotta S, Alagia M, Attaianese F, Verde A, Tarallo A, Gragnaniello V, Ziagaki A, Guimaraes MJ, Aguiar P, Hahn A, Azevedo O, Donati MA, Kiec-Wilk B, Scarpa M, van der Beek NAME, Del Toro Riera M, Germain DP, Huidekoper H, van den Hout JMP, van der Ploeg AT; and the MetabERN Subnetwork for Lysosomal Disorders. Parenti G, et al. Orphanet J Rare Dis. 2024 Nov 1;19(1):408. doi: 10.1186/s13023-024-03373-w. Orphanet J Rare Dis. 2024. PMID: 39482698 Free PMC article. Review.
Pediatric Scleritis: An Update.
Tarsia M, Gaggiano C, Gessaroli E, Grosso S, Tosi GM, Frediani B, Cantarini L, Fabiani C. Tarsia M, et al. Among authors: grosso s. Ocul Immunol Inflamm. 2023 Jan;31(1):175-184. doi: 10.1080/09273948.2021.2023582. Epub 2022 Feb 28. Ocul Immunol Inflamm. 2023. PMID: 35226583
Oxidative stress in epilepsy.
Geronzi U, Lotti F, Grosso S. Geronzi U, et al. Among authors: grosso s. Expert Rev Neurother. 2018 May;18(5):427-434. doi: 10.1080/14737175.2018.1465410. Epub 2018 Apr 19. Expert Rev Neurother. 2018. PMID: 29651881 Review.
YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse.
Denommé-Pichon AS, Collins SC, Bruel AL, Mikhaleva A, Wagner C, Vancollie VE, Thomas Q, Chevarin M, Weber M, Prada CE, Overs A, Palomares-Bralo M, Santos-Simarro F, Pacio-Míguez M, Busa T, Legius E, Bacino CA, Rosenfeld JA, Le Guyader G, Egloff M, Le Guillou X, Mencarelli MA, Renieri A, Grosso S, Levy J, Dozières B, Desguerre I, Vitobello A, Duffourd Y, Lelliott CJ, Thauvin-Robinet C, Philippe C, Faivre L, Yalcin B. Denommé-Pichon AS, et al. Among authors: grosso s. Genet Med. 2023 Jul;25(7):100835. doi: 10.1016/j.gim.2023.100835. Epub 2023 Mar 28. Genet Med. 2023. PMID: 36999555 Free article. Review.
Antiepileptic drugs: Role in paediatric poisoning.
Ferranti S, Grande E, Gaggiano C, Grosso S. Ferranti S, et al. Among authors: grosso s. J Paediatr Child Health. 2018 May;54(5):475-479. doi: 10.1111/jpc.13833. Epub 2018 Jan 2. J Paediatr Child Health. 2018. PMID: 29292550 Review.
Coffin-Siris syndrome and epilepsy.
Curcio MR, Ferranti S, Lotti F, Grosso S. Curcio MR, et al. Among authors: grosso s. Neurol Sci. 2021 Feb;42(2):727-729. doi: 10.1007/s10072-020-04782-y. Epub 2020 Oct 2. Neurol Sci. 2021. PMID: 33006724
Rare variants modulating phenotype in NF1 carriers.
Pasquinelli E, Casamassima G, Brunelli G, Belakhdar O, Minetto S, Grosso S, Canitano R, Marsili S, Martellucci I, Miano ST, Petrioli R, Baldassarri M, D'Aurizio R, Fallerini C, Renieri A. Pasquinelli E, et al. Among authors: grosso s. Sci Rep. 2025 Jul 13;15(1):25337. doi: 10.1038/s41598-025-09751-z. Sci Rep. 2025. PMID: 40653509 Free PMC article.
370 results