Menni F - Search Results

1

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.

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

Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndrome.

Esposito S, Selicorni A, Daleno C, Valzano A, Cerutti M, Galeone C, Consolo S, Menni F, Principi N. Esposito S, et al. Among authors: menni f. Hum Vaccin. 2011 Jun;7(6):613-7. doi: 10.4161/hv.7.6.15133. Epub 2011 Jun 1. Hum Vaccin. 2011. PMID: 21508673

4

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

5

Neonatal atypical hemolytic uremic syndrome due to methylmalonic aciduria and homocystinuria.

Menni F, Testa S, Guez S, Chiarelli G, Alberti L, Esposito S. Menni F, et al. Pediatr Nephrol. 2012 Aug;27(8):1401-5. doi: 10.1007/s00467-012-2152-6. Epub 2012 Mar 25. Pediatr Nephrol. 2012. PMID: 22447314

6

Severe vitamin B12 deficiency in an exclusively breastfed 5-month-old Italian infant born to a mother receiving multivitamin supplementation during pregnancy.

Guez S, Chiarelli G, Menni F, Salera S, Principi N, Esposito S. Guez S, et al. Among authors: menni f. BMC Pediatr. 2012 Jun 24;12:85. doi: 10.1186/1471-2431-12-85. BMC Pediatr. 2012. PMID: 22726312 Free PMC article.

7

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.

8

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

9

Preliminary data on immunogenicity, safety and tolerability of trivalent inactivated influenza vaccine in children with inborn errors of metabolism at risk of decompensation.

Esposito S, Salvini F, Menni F, Scala A, Salvatici E, Manzoni F, Riva E, Giovannini M, Principi N. Esposito S, et al. Among authors: menni f. Vaccine. 2013 Oct 25;31(45):5149-51. doi: 10.1016/j.vaccine.2013.08.058. Epub 2013 Sep 5. Vaccine. 2013. PMID: 24012567 Free article. Clinical Trial.

10

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

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