Ferrari F - Search Results

1

Pure segmental trisomy 1q42-qter in a boy with a severe phenotype.

Percesepe A, Lugli L, Pierluigi M, Cavani S, Malacarne M, Roversi MF, Ferrari F, Forabosco A. Percesepe A, et al. Among authors: ferrari f. Am J Med Genet A. 2007 Oct 1;143A(19):2339-42. doi: 10.1002/ajmg.a.31890. Am J Med Genet A. 2007. PMID: 17702013 No abstract available.

2

Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele.

Percesepe A, Bertucci E, Ferrari P, Lugli L, Ferrari F, Mazza V, Forabosco A. Percesepe A, et al. Among authors: ferrari f, ferrari p. Prenat Diagn. 2008 May;28(5):447-9. doi: 10.1002/pd.1991. Prenat Diagn. 2008. PMID: 18395877 No abstract available.

3

A 12.4 Mb direct duplication in 19q12-q13 in a boy with cardiac and CNS malformations and developmental delay.

Lugli L, Malacarne M, Cavani S, Pierluigi M, Ferrari F, Percesepe A. Lugli L, et al. Among authors: ferrari f. J Appl Genet. 2011 Aug;52(3):335-9. doi: 10.1007/s13353-011-0033-5. Epub 2011 Mar 3. J Appl Genet. 2011. PMID: 21369844

4

A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.

Elmakky A, Carli D, Lugli L, Torelli P, Guidi B, Falcinelli C, Fini S, Ferrari F, Percesepe A. Elmakky A, et al. Among authors: ferrari f. Eur J Med Genet. 2014 Mar;57(4):145-50. doi: 10.1016/j.ejmg.2014.02.005. Epub 2014 Feb 18. Eur J Med Genet. 2014. PMID: 24556499

5

Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement.

Lugli L, Just W, Genovese E, Palma S, Ferrari F, Percesepe A. Lugli L, et al. Among authors: ferrari f. Clin Dysmorphol. 2015 Jan;24(1):17-20. doi: 10.1097/MCD.0000000000000061. Clin Dysmorphol. 2015. PMID: 25325184 No abstract available.

6

Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester.

Bertucci E, Mazza V, Lugli L, Ferrari F, Stanghellini I, Percesepe A. Bertucci E, et al. Among authors: ferrari f. J Obstet Gynaecol Res. 2015 Nov;41(11):1831-4. doi: 10.1111/jog.12791. Epub 2015 Jul 30. J Obstet Gynaecol Res. 2015. PMID: 26227013

7

Massive thymic hemorrhage and hemothorax occurring in utero.

Gargano G, Paltrinieri AL, Gallo C, Di Pancrazio L, Roversi MF, Ferrari F. Gargano G, et al. Among authors: ferrari f. Ital J Pediatr. 2015 Nov 14;41:88. doi: 10.1186/s13052-015-0196-5. Ital J Pediatr. 2015. PMID: 26568429 Free PMC article.

8

Pre- and post-natal growth in two sisters with 3-M syndrome.

Lugli L, Bertucci E, Mazza V, Elmakky A, Ferrari F, Neuhaus C, Percesepe A. Lugli L, et al. Among authors: ferrari f. Eur J Med Genet. 2016 Apr;59(4):232-6. doi: 10.1016/j.ejmg.2016.01.009. Epub 2016 Feb 2. Eur J Med Genet. 2016. PMID: 26850509

9

Persistent intestinal bleeding due to severe CMV-related thrombocytopenia in a preterm newborn.

Berardi A, Spaggiari E, Cattelani C, Roversi MF, Pecorari M, Lazzarotto T, Ferrari F. Berardi A, et al. Among authors: ferrari f. J Matern Fetal Neonatal Med. 2018 May;31(9):1246-1249. doi: 10.1080/14767058.2017.1312331. Epub 2017 Apr 11. J Matern Fetal Neonatal Med. 2018. PMID: 28395563

10

Foot-to-Foot Contact Among Initial Goal-Directed Movements Supports the Prognostic Value of Fidgety Movements in HIE-Cooled Infants.

Ferrari F, Bedetti L, Bertoncelli N, Roversi MF, Della Casa E, Guidotti I, Ori L, D'Amico R, Valeri L, Lugli L, Lucaccioni L, Berardi A. Ferrari F, et al. Front Pediatr. 2022 Jan 5;9:731021. doi: 10.3389/fped.2021.731021. eCollection 2021. Front Pediatr. 2022. PMID: 35071123 Free PMC article.

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