Boito S - Search Results

1

Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?

Beltrami B, Cerasani J, Consales A, Villa R, Resta N, Loconte DC, Boito S, Caschera L, Bassi L, Colombo L, Iascone M, Bedeschi MF. Beltrami B, et al. Among authors: boito s. Clin Case Rep. 2022 Aug 22;10(8):e6256. doi: 10.1002/ccr3.6256. eCollection 2022 Aug. Clin Case Rep. 2022. PMID: 36017115 Free PMC article.

2

Customized Fetal Growth Charts for Parents' Characteristics, Race, and Parity by Quantile Regression Analysis: A Cross-sectional Multicenter Italian Study.

Ghi T, Cariello L, Rizzo L, Ferrazzi E, Periti E, Prefumo F, Stampalija T, Viora E, Verrotti C, Rizzo G; Società Italiana di Ecografia Ostetrica e Ginecologica Working Group on Fetal Biometric Charts. Ghi T, et al. J Ultrasound Med. 2016 Jan;35(1):83-92. doi: 10.7863/ultra.15.03003. Epub 2015 Dec 7. J Ultrasound Med. 2016. PMID: 26643757

3

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

4

Prenatal ultrasound factors and genetic disorders in pregnancies complicated by polyhydramnios.

Boito S, Crovetto F, Ischia B, Crippa BL, Fabietti I, Bedeschi MF, Lalatta F, Colombo L, Mosca F, Fedele L, Persico N. Boito S, et al. Prenat Diagn. 2016 Aug;36(8):726-30. doi: 10.1002/pd.4851. Epub 2016 Jun 24. Prenat Diagn. 2016. PMID: 27247190

5

Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome.

Peron A, Boito S, Rizzuti T, Borzani I, Baccarin M, Bedeschi MF, Lalatta F. Peron A, et al. Among authors: boito s. Genet Med. 2018 Nov;20(11):1483-1484. doi: 10.1038/gim.2018.19. Genet Med. 2018. PMID: 29517766 Free article. No abstract available.

6

Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis: insights from a multicentre study.

Conte G, Caschera L, Parazzini C, Cinnante C, Izzo G, Talenti G, Severino M, Ormitti F, Palumbo G, Pinelli L, Antonelli A, Manganaro L, Boito S, Rossi A, Triulzi F, Righini A. Conte G, et al. Among authors: boito s. Eur Radiol. 2020 Apr;30(4):2161-2170. doi: 10.1007/s00330-019-06538-5. Epub 2020 Jan 3. Eur Radiol. 2020. PMID: 31900695

7

Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome.

Rinaldi B, Cesaretti C, Boito S, Villa R, Guerneri S, Borzani I, Rizzuti T, Marchetti D, Conte G, Cinnante C, Triulzi F, Persico N, Iascone M, Natacci F. Rinaldi B, et al. Among authors: boito s. Prenat Diagn. 2022 Jun;42(7):927-933. doi: 10.1002/pd.6171. Epub 2022 May 27. Prenat Diagn. 2022. PMID: 35584264

8

Prenatal ultrasound findings associated with PIGW variants: One more piece in the FRYNS syndrome puzzle? PIGW-related prenatal findings.

Ronzoni L, Boito S, Meossi C, Cesaretti C, Rinaldi B, Agolini E, Rizzuti T, Pezzoli L, Silipigni R, Novelli A, Iascone M, Persico N, Natacci F. Ronzoni L, et al. Among authors: boito s. Prenat Diagn. 2022 Nov;42(12):1493-1502. doi: 10.1002/pd.6204. Epub 2022 Jul 19. Prenat Diagn. 2022. PMID: 35788948 Review.

9

Congenital diaphragmatic hernia in Coffin Siris syndrome: Further evidence from two cases.

Rimoldi M, Rinaldi B, Villa R, Cerasani J, Beltrami B, Iascone M, Silipigni R, Boito S, Gangi S, Colombo L, Porro M, Cesaretti C, Bedeschi MF. Rimoldi M, et al. Among authors: boito s. Am J Med Genet A. 2023 Feb;191(2):605-611. doi: 10.1002/ajmg.a.63054. Epub 2022 Nov 23. Am J Med Genet A. 2023. PMID: 36416235

10

CTNND1-Related Disorder: New Insight on Prenatal Phenotype.

Conti B, Di Napoli C, Hafdaoui S, Nicotra V, Cesaretti C, Runza L, Accurti V, Boito S, Iascone M, Marchetti D, Silipigni R, Finelli P, Natacci F. Conti B, et al. Among authors: boito s. Am J Med Genet A. 2024 Nov 1:e63921. doi: 10.1002/ajmg.a.63921. Online ahead of print. Am J Med Genet A. 2024. PMID: 39487033

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