Milani D - Search Results

1

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. Cytogenet Genome Res. 2012;136(3):167-70. doi: 10.1159/000336979. Epub 2012 Mar 7. Cytogenet Genome Res. 2012. PMID: 22398643

2

Biliary atresia and Kabuki syndrome: another case with long-term follow-up.

Selicorni A, Colombo C, Bonato S, Milani D, Giunta AM, Bedeschi MF. Selicorni A, et al. Among authors: milani d. Am J Med Genet. 2001 May 1;100(3):251. doi: 10.1002/ajmg.1253. Am J Med Genet. 2001. PMID: 11343312 No abstract available.

3

De novo duplication of chromosome 13(q32-q34) in a child with developmental delay.

Milani D, D'Arrigo S, Guerneri S, Selicorni A, Riva D, Pantaleoni C. Milani D, et al. Among authors: d arrigo s. J Child Neurol. 2006 Dec;21(12):1084-5. doi: 10.1177/7010.2006.00229. J Child Neurol. 2006. PMID: 17156706

4

Otitis media with effusion and hearing loss in children with Cornelia de Lange syndrome.

Marchisio P, Selicorni A, Pignataro L, Milani D, Baggi E, Lambertini L, Dusi E, Villa L, Capaccio P, Cerutti M, Esposito S, Principi N. Marchisio P, et al. Among authors: milani d. Am J Med Genet A. 2008 Feb 15;146A(4):426-32. doi: 10.1002/ajmg.a.32183. Am J Med Genet A. 2008. PMID: 18203151

5

Analysis of congenital heart defects in 87 consecutive patients with Brachmann-de Lange syndrome.

Selicorni A, Colli AM, Passarini A, Milani D, Cereda A, Cerutti M, Maitz S, Alloni V, Salvini L, Galli MA, Ghiglia S, Salice P, Danzi GB. Selicorni A, et al. Among authors: milani d. Am J Med Genet A. 2009 Jun;149A(6):1268-72. doi: 10.1002/ajmg.a.32838. Am J Med Genet A. 2009. PMID: 19449412

6

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: milani d. 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

7

High frequency of copy number imbalances in Rubinstein-Taybi patients negative to CREBBP mutational analysis.

Gervasini C, Mottadelli F, Ciccone R, Castronovo P, Milani D, Scarano G, Bedeschi MF, Belli S, Pilotta A, Selicorni A, Zuffardi O, Larizza L. Gervasini C, et al. Among authors: milani d. Eur J Hum Genet. 2010 Jul;18(7):768-75. doi: 10.1038/ejhg.2010.1. Epub 2010 Feb 3. Eur J Hum Genet. 2010. PMID: 20125191 Free PMC article.

8

Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patients.

Bedeschi MF, Bianchi V, Colli AM, Natacci F, Cereda A, Milani D, Maitz S, Lalatta F, Selicorni A. Bedeschi MF, et al. Among authors: milani d. Am J Med Genet A. 2011 Feb;155A(2):353-9. doi: 10.1002/ajmg.a.33819. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271653

9

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: milani d. J Child Neurol. 2014 Sep;29(9):NP74-7. doi: 10.1177/0883073813503187. Epub 2013 Sep 23. J Child Neurol. 2014. PMID: 24065579

10

Syndromic obesity: clinical implications of a correct diagnosis.

Milani D, Cerutti M, Pezzani L, Maffei P, Milan G, Esposito S. Milani D, et al. Ital J Pediatr. 2014 Apr 2;40(1):33. doi: 10.1186/1824-7288-40-33. Ital J Pediatr. 2014. PMID: 24690487 Free PMC article.

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