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

Year Number of Results
1998 2
1999 1
2001 1
2002 1
2003 1
2004 1
2006 1
2007 1
2008 2
2009 2
2011 1
2012 4
2013 4
2014 4
2015 7
2016 3
2017 5
2018 3
2019 1
2020 1
2021 2
2022 2
2023 3
2024 3
2025 5
2026 2

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58 results

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Page 1
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome.
Manzoni E, Carli S, Gaignard P, Schlieben LD, Hirano M, Ronchi D, Gonzales E, Shimura M, Murayama K, Okazaki Y, Barić I, Petkovic Ramadza D, Karall D, Mayr J, Martinelli D, La Morgia C, Primiano G, Santer R, Servidei S, Bris C, Cano A, Furlan F, Gasperini S, Laborde N, Lamperti C, Lenz D, Mancuso M, Montano V, Menni F, Musumeci O, Nesbitt V, Procopio E, Rouzier C, Staufner C, Taanman JW, Tal G, Ticci C, Cordelli DM, Carelli V, Procaccio V, Prokisch H, Garone C. Manzoni E, et al. Among authors: menni f. Brain Commun. 2024 May 6;6(3):fcae160. doi: 10.1093/braincomms/fcae160. eCollection 2024. Brain Commun. 2024. PMID: 38756539 Free PMC article.
Nutritional Challenges in Duchenne Muscular Dystrophy.
Salera S, Menni F, Moggio M, Guez S, Sciacco M, Esposito S. Salera S, et al. Among authors: menni f. Nutrients. 2017 Jun 10;9(6):594. doi: 10.3390/nu9060594. Nutrients. 2017. PMID: 28604599 Free PMC article. Review.
Late-onset Pompe's disease in pediatrics: results from an Italian national survey on 38 patients and proposal of a targeted diagnostic algorithm.
Spada M, Gasperini S, Filosto M, Astrea G, Bracci B, Bruno C, Burlina A, Cavallini A, Concolino D, Crescitelli V, D'Amico A, Deodato F, Dionisi-Vici C, Donati MA, Fecarotta S, Fischetto R, Fiumara A, Furlan F, Gragnaniello V, Mala D, Marica M, Menni F, Pagliardini V, Panicucci C, Parenti G, Pession A, Ricci F, Rovelli V, Sacchini M, Santorelli FM, Santoro L, Scarpa M, Taurisano R, Tummolo A, Porta F. Spada M, et al. Among authors: menni f. Orphanet J Rare Dis. 2025 Nov 28;20(1):616. doi: 10.1186/s13023-025-04063-x. Orphanet J Rare Dis. 2025. PMID: 41316280 Free PMC article.
Electroclinical phenotype in Rubinstein-Taybi syndrome.
Giacobbe A, Ajmone PF, Milani D, Avignone S, Triulzi F, Gervasini C, Menni F, Monti F, Biffi D, Canavesi K, Costantino MA. Giacobbe A, et al. Among authors: menni f. Brain Dev. 2016 Jun;38(6):563-70. doi: 10.1016/j.braindev.2015.12.003. Epub 2016 Feb 8. Brain Dev. 2016. PMID: 26867510
Expanded Newborn Screening in Italy: The First Report of Lombardy Region.
Berardo C, Vasco A, Mauri A, Lucchi S, Cappelletti L, Saielli L, Rizzetto M, Biganzoli D, Montrasio C, Postorivo D, Pratiffi E, Meta A, Carelli S, Amorosi A, Paci S, Cefalo G, Furlan F, Menni F, Gasperini S, Crescitelli V, Banderali G, Zuccotti G, Alberti L, Cereda C. Berardo C, et al. Among authors: menni f. Int J Neonatal Screen. 2025 Apr 25;11(2):31. doi: 10.3390/ijns11020031. Int J Neonatal Screen. 2025. PMID: 40407514 Free PMC article.
Is it time to change the neurofibromatosis 1 diagnostic criteria?
Tadini G, Milani D, Menni F, Pezzani L, Sabatini C, Esposito S. Tadini G, et al. Among authors: menni f. Eur J Intern Med. 2014 Jul;25(6):506-10. doi: 10.1016/j.ejim.2014.04.004. Epub 2014 Apr 29. Eur J Intern Med. 2014. PMID: 24784952 Review.
Think about it: FMR1 gene mosaicism.
Bonarrigo FA, Russo S, Vizziello P, Menni F, Cogliati F, Giorgini V, Monti F, Milani D. Bonarrigo FA, et al. Among authors: menni f. J Child Neurol. 2014 Sep;29(9):NP74-7. doi: 10.1177/0883073813503187. Epub 2013 Sep 23. J Child Neurol. 2014. PMID: 24065579
58 results