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

Year Number of Results
2003 1
2004 1
2007 1
2008 2
2009 2
2011 1
2012 3
2013 4
2014 4
2015 6
2016 3
2017 5
2018 2
2019 1
2020 1
2021 3
2022 2
2023 3
2024 0

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39 results

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Page 1
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.
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.
Vaccination in children with inborn errors of metabolism.
Menni F, Chiarelli G, Sabatini C, Principi N, Esposito S. Menni F, et al. Vaccine. 2012 Nov 26;30(50):7161-4. doi: 10.1016/j.vaccine.2012.10.012. Epub 2012 Oct 18. Vaccine. 2012. PMID: 23085362 Review.
Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium.
Ditters IAM, Huidekoper HH, Kruijshaar ME, Rizopoulos D, Hahn A, Mongini TE, Labarthe F, Tardieu M, Chabrol B, Brassier A, Parini R, Parenti G, van der Beek NAME, van der Ploeg AT, van den Hout JMP; European Pompe Consortium project group on classic infantile Pompe disease. Ditters IAM, et al. Lancet Child Adolesc Health. 2022 Jan;6(1):28-37. doi: 10.1016/S2352-4642(21)00308-4. Epub 2021 Nov 22. Lancet Child Adolesc Health. 2022. PMID: 34822769
Treatment of neurofibromatosis type 1.
Sabatini C, Milani D, Menni F, Tadini G, Esposito S. Sabatini C, et al. Among authors: menni f. Curr Treat Options Neurol. 2015 Jun;17(6):355. doi: 10.1007/s11940-015-0355-4. Curr Treat Options Neurol. 2015. PMID: 25917340
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
A multidisciplinary approach in neurofibromatosis 1.
Milani D, Pezzani L, Tadini G, Menni F, Esposito S. Milani D, et al. Among authors: menni f. Lancet Neurol. 2015 Jan;14(1):29-30. doi: 10.1016/S1474-4422(14)70255-8. Lancet Neurol. 2015. PMID: 25496892 No abstract available.
Hyperammonemia Syndrome After Lung Transplantation: A Double-Hit Fatal Syndrome. A Case Report.
Cattaneo V, Caccioppola A, Colombo SM, Scaravilli V, Tubiolo D, Crotti S, Bosone M, Rafaniello Raviele P, Olmeda E, Menni F, Furlan F, Rossetti V, Damarco F, Panigada M, Grasselli G. Cattaneo V, et al. Among authors: menni f. Transplant Proc. 2023 Oct;55(8):1991-1994. doi: 10.1016/j.transproceed.2023.07.003. Epub 2023 Aug 2. Transplant Proc. 2023. PMID: 37537075
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
39 results