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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 3
2011 1
2012 4
2013 4
2014 4
2015 7
2016 3
2017 5
2018 3
2019 1
2020 1
2021 3
2022 3
2023 3
2024 1

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51 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.
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
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.
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy.
Ronchi D, Garbellini M, Magri F, Menni F, Meneri M, Bedeschi MF, Dilena R, Cecchetti V, Picciolli I, Furlan F, Polimeni V, Salani S, Pezzoli L, Fortunato F, Bellini M, Piga D, Ripolone M, Zanotti S, Napoli L, Ciscato P, Sciacco M, Mangili G, Mosca F, Corti S, Iascone M, Comi GP. Ronchi D, et al. Among authors: menni f. Eur J Hum Genet. 2023 Dec;31(12):1414-1420. doi: 10.1038/s41431-023-01433-6. Epub 2023 Jul 19. Eur J Hum Genet. 2023. PMID: 37468577
Hyperinsulinism plus hyperammonemia.
Parini R, Colombo F, Lombardi AM, Menni F, Beccaria L. Parini R, et al. Among authors: menni f. J Pediatr. 1998 Dec;133(6):800-1. doi: 10.1016/s0022-3476(98)70158-1. J Pediatr. 1998. PMID: 9842050 No abstract available.
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.
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
51 results