Fogliani R - Search Results

1

Author's reply regarding "Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome".

Baffero GM, Somigliana E, Crovetto F, Paffoni A, Persico N, Guerneri S, Lalatta F, Fogliani R, Fedele L. Baffero GM, et al. Among authors: fogliani r. Prenat Diagn. 2013 Mar;33(3):303-4. doi: 10.1002/pd.4046. Prenat Diagn. 2013. PMID: 23456997 No abstract available.

2

Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome.

Baffero GM, Somigliana E, Crovetto F, Paffoni A, Persico N, Guerneri S, Lalatta F, Fogliani R, Fedele L. Baffero GM, et al. Among authors: fogliani r. Prenat Diagn. 2012 Nov;32(11):1102-8. doi: 10.1002/pd.3965. Epub 2012 Sep 7. Prenat Diagn. 2012. PMID: 22961322

3

Prenatal ultrasound predictors of postnatal major cerebral abnormalities in fetuses with apparently isolated mild ventriculomegaly.

Baffero GM, Crovetto F, Fabietti I, Boito S, Fogliani R, Fumagalli M, Triulzi F, Mosca F, Fedele L, Persico N. Baffero GM, et al. Among authors: fogliani r. Prenat Diagn. 2015 Aug;35(8):783-8. doi: 10.1002/pd.4607. Epub 2015 May 24. Prenat Diagn. 2015. PMID: 25900107

4

Prenatal confirmation of trisomy 12 mosaicism by fetal skin biopsy.

Cartolano R, Guerneri S, Fogliani R, Galimberti A, Nicolini U. Cartolano R, et al. Among authors: fogliani r. Prenat Diagn. 1993 Nov;13(11):1057-9. doi: 10.1002/pd.1970131110. Prenat Diagn. 1993. PMID: 8140069

5

Prenatal diagnosis of genetic syndromes may be facilitated by serendipitous findings at fetal blood sampling.

Lalatta F, Salmona S, Fogliani R, Rizzuti T, Nicolini U. Lalatta F, et al. Among authors: fogliani r. Prenat Diagn. 1998 Aug;18(8):834-7. Prenat Diagn. 1998. PMID: 9742573

6

Prenatal and postnatal findings in five cases of Fryns syndrome.

Peron A, Bedeschi MF, Fabietti I, Baffero GM, Fogliani R, Ciralli F, Mosca F, Rizzuti T, Leva E, Lalatta F. Peron A, et al. Among authors: fogliani r. Prenat Diagn. 2014 Dec;34(12):1227-30. doi: 10.1002/pd.4447. Epub 2014 Jul 22. Prenat Diagn. 2014. PMID: 24996149 No abstract available.

7

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: fogliani r. 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.

8

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: fogliani r. 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.

9

Unusual prenatal presentation of Rubinstein-Taybi syndrome: a case report.

Bedeschi MF, Crippa BL, Colombo L, Guez S, Cerruti M, Fogliani R, Gervasini C, Lalatta F. Bedeschi MF, et al. Among authors: fogliani r. Am J Med Genet A. 2014 Oct;164A(10):2663-6. doi: 10.1002/ajmg.a.36684. Epub 2014 Jul 29. Am J Med Genet A. 2014. PMID: 25073882

10

Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.

Lalatta F, Folliero E, Cavallari U, Di Segni M, Gentilin B, Fogliani R, Quagliarini D, Vizziello P, Monti F, Gargantini L. Lalatta F, et al. Among authors: fogliani r. Ital J Pediatr. 2012 Oct 3;38:52. doi: 10.1186/1824-7288-38-52. Ital J Pediatr. 2012. PMID: 23034220 Free PMC article.

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