Bianchi V - Search Results

1

When and how ruling out cystic fibrosis in adult patients with bronchiectasis.

Gramegna A, Aliberti S, Seia M, Porcaro L, Bianchi V, Castellani C, Melotti P, Sorio C, Consalvo E, Franceschi E, Amati F, Contarini M, Gaffuri M, Roncoroni L, Vigone B, Bellofiore A, Del Monaco C, Oriano M, Terranova L, Patria MF, Marchisio P, Assael BM, Blasi F. Gramegna A, et al. Among authors: bianchi v. Multidiscip Respir Med. 2018 Aug 9;13(Suppl 1):29. doi: 10.1186/s40248-018-0142-7. eCollection 2018. Multidiscip Respir Med. 2018. PMID: 30151190 Free PMC article. Review.

2

An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests.

Castellani C, Perobelli S, Bianchi V, Seia M, Melotti P, Zanolla L, Assael BM, Lalatta F. Castellani C, et al. Among authors: bianchi v. Am J Med Genet A. 2011 Apr;155A(4):778-85. doi: 10.1002/ajmg.a.33870. Epub 2011 Mar 17. Am J Med Genet A. 2011. PMID: 21416590 Clinical Trial.

3

Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.

Ronzoni L, Peron A, Bianchi V, Baccarin M, Guerneri S, Silipigni R, Lalatta F, Bedeschi MF. Ronzoni L, et al. Among authors: bianchi v. Am J Med Genet A. 2015 Jul;167(7):1551-9. doi: 10.1002/ajmg.a.37063. Epub 2015 Apr 6. Am J Med Genet A. 2015. PMID: 25851921

4

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: bianchi v. 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

5

Prevalence of diabetes and pre-diabetes in a cohort of Italian young adults with Williams syndrome.

Masserini B, Bedeschi MF, Bianchi V, Scuvera G, Beck-Peccoz P, Lalatta F, Selicorni A, Orsi E. Masserini B, et al. Among authors: bianchi v. Am J Med Genet A. 2013 Apr;161A(4):817-21. doi: 10.1002/ajmg.a.35655. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495209

6

Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene.

Bedeschi MF, Novelli A, Bernardini L, Parazzini C, Bianchi V, Torres B, Natacci F, Giuffrida MG, Ficarazzi P, Dallapiccola B, Lalatta F. Bedeschi MF, et al. Among authors: bianchi v. Am J Med Genet A. 2008 Jul 1;146A(13):1718-24. doi: 10.1002/ajmg.a.32365. Am J Med Genet A. 2008. PMID: 18512229

7

Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations.

Cesaretti C, Gentilin B, Bianchi V, Melloni G, Bonaguro M, Rossi C, Meazzini C, Brusati R, Lalatta F. Cesaretti C, et al. Among authors: bianchi v. Clin Dysmorphol. 2011 Oct;20(4):229-231. doi: 10.1097/MCD.0b013e3283491725. Clin Dysmorphol. 2011. PMID: 21772136 No abstract available.

8

Prenatal phenotype of Nager syndrome and Rodriguez syndrome: variable expression of the same entity?

Gana S, Gentilin B, Bianchi V, Gorla S, Ceriani F, Melloni G, Lalatta F. Gana S, et al. Among authors: bianchi v. Clin Dysmorphol. 2013 Oct;22(4):135-139. doi: 10.1097/MCD.0b013e32836351c8. Clin Dysmorphol. 2013. PMID: 23811969 No abstract available.

9

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Gentilin B, Guerneri S, Bianchi V, Natacci F, Colombo A, Fogliani R, Fortuna R, Coviello DA, Curcio C, Lalatta F. Gentilin B, et al. Among authors: bianchi v. Twin Res Hum Genet. 2008 Jun;11(3):352-6. doi: 10.1375/twin.11.3.352. Twin Res Hum Genet. 2008. PMID: 18498214 Review.

10

Recurrence of a severe multiple congenital anomaly syndrome characterized by micrognathia, microtia, cleft palate, and short neck in two siblings.

Natacci F, Bianchi V, Guerneri S, Rizzuti T, Boito S, Gentilin B, Bedeschi MF, Lalatta F. Natacci F, et al. Among authors: bianchi v. Clin Dysmorphol. 2009 Jan;18(1):45-48. doi: 10.1097/MCD.0b013e328317c867. Clin Dysmorphol. 2009. PMID: 19050404 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

630 results

Search Page

Filters