Natacci F - Search Results

1

Double pituitary and conserved function in an adult patient with neurofibromatosis type 1.

Filopanti M, Verga U, Ermetici F, Natacci F, Lalatta F, Avignone S, Trespidi L, Beck-Peccoz P, Mantovani G, Lania AG, Spada A. Filopanti M, et al. Among authors: natacci f. J Clin Endocrinol Metab. 2011 Jul;96(7):1953-4. doi: 10.1210/jc.2011-0451. J Clin Endocrinol Metab. 2011. PMID: 21734002 No abstract available.

2

Nasopharyngeal teratoma and diaphragmatic hernia: a non random association?

Natacci F, Moschetta M, Bedeschi MF, Spaccini L, Capelli A, Segni MD, Rizzuti T, Mosca F, Lalatta F. Natacci F, et al. Clin Dysmorphol. 2004 Oct;13(4):255-256. Clin Dysmorphol. 2004. PMID: 15365464

3

The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration.

Nicolini U, Lalatta F, Natacci F, Curcio C, Bui TH. Nicolini U, et al. Among authors: natacci f. Hum Reprod Update. 2004 Nov-Dec;10(6):541-8. doi: 10.1093/humupd/dmh046. Hum Reprod Update. 2004. PMID: 15514017 Review.

4

Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expression.

Bedeschi MF, Escande F, Bellini M, Natacci F, Cavallari U, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Clin Dysmorphol. 2006 Oct;15(4):239-241. doi: 10.1097/01.mcd.0000220618.01144.6d. Clin Dysmorphol. 2006. PMID: 16957482

5

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: natacci f. 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.

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: natacci f. 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

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. Clin Dysmorphol. 2009 Jan;18(1):45-48. doi: 10.1097/MCD.0b013e328317c867. Clin Dysmorphol. 2009. PMID: 19050404 No abstract available.

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: natacci f. 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

Prenatal manifestation and management of a mother and child affected by spondyloperipheral dysplasia with a C-propeptide mutation in COL2A1: case report.

Bedeschi MF, Bianchi V, Gentilin B, Colombo L, Natacci F, Giglio S, Andreucci E, Trespidi L, Acaia B, Furga AS, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Orphanet J Rare Dis. 2011 Feb 28;6:7. doi: 10.1186/1750-1172-6-7. Orphanet J Rare Dis. 2011. PMID: 21356074 Free PMC article.

10

Neurofibromatosis type 1 and pregnancy: maternal complications and attitudes about prenatal diagnosis.

Cesaretti C, Melloni G, Quagliarini D, Fogliani R, Zaina B, Bedeschi MF, Lalatta F, Trespidi L, Natacci F. Cesaretti C, et al. Among authors: natacci f. Am J Med Genet A. 2013 Feb;161A(2):386-8. doi: 10.1002/ajmg.a.35720. Epub 2013 Jan 16. Am J Med Genet A. 2013. PMID: 23325535 No abstract available.

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