Menni F - Search Results

1

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

2

Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome.

Olioso G, Passarini A, Atzeri F, Milani D, Cereda A, Cerutti M, Maitz S, Menni F, Selicorni A. Olioso G, et al. Among authors: menni f. Am J Med Genet A. 2009 Nov;149A(11):2532-7. doi: 10.1002/ajmg.a.33075. Am J Med Genet A. 2009. PMID: 19876900

3

De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders.

Milani D, Bedeschi MF, Iascone M, Chiarelli G, Cerutti M, Menni F. Milani D, et al. Among authors: menni f. Cytogenet Genome Res. 2012;136(3):167-70. doi: 10.1159/000336979. Epub 2012 Mar 7. Cytogenet Genome Res. 2012. PMID: 22398643

4

Healthcare transition in patients with rare genetic disorders with and without developmental disability: neurofibromatosis 1 and Williams-Beuren syndrome.

Van Lierde A, Menni F, Bedeschi MF, Natacci F, Guez S, Vizziello P, Costantino MA, Lalatta F, Esposito S. Van Lierde A, et al. Among authors: menni f. Am J Med Genet A. 2013 Jul;161A(7):1666-74. doi: 10.1002/ajmg.a.35982. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696535

5

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.

6

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.

7

Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management.

Milani D, Manzoni FM, Pezzani L, Ajmone P, Gervasini C, Menni F, Esposito S. Milani D, et al. Among authors: menni f. Ital J Pediatr. 2015 Jan 20;41:4. doi: 10.1186/s13052-015-0110-1. Ital J Pediatr. 2015. PMID: 25599811 Free PMC article. Review.

8

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

9

Vaccination coverage of children with rare genetic diseases and attitudes of their parents toward vaccines.

Esposito S, Cerutti M, Milani D, Menni F, Principi N. Esposito S, et al. Among authors: menni f. Hum Vaccin Immunother. 2016 Mar 3;12(3):801-5. doi: 10.1080/21645515.2015.1086046. Hum Vaccin Immunother. 2016. PMID: 26337545 Free PMC article.

10

Hepatoblastoma in Rubinstein-Taybi Syndrome: A Case Report.

Milani D, Bonarrigo FA, Menni F, Spaccini L, Gervasini C, Esposito S. Milani D, et al. Among authors: menni f. Pediatr Blood Cancer. 2016 Mar;63(3):572-3. doi: 10.1002/pbc.25806. Epub 2015 Oct 20. Pediatr Blood Cancer. 2016. PMID: 26485669 No abstract available.

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