Rizzuti T - Search Results

1

Histological characterization of placenta in COVID19 pregnant women.

Cribiù FM, Croci GA, Del Gobbo A, Rizzuti T, Iurlaro E, Tondo M, Viscardi A, Bosari S, Ferrero S. Cribiù FM, et al. Among authors: rizzuti t. Eur J Obstet Gynecol Reprod Biol. 2020 Sep;252:619-621. doi: 10.1016/j.ejogrb.2020.06.041. Epub 2020 Jun 23. Eur J Obstet Gynecol Reprod Biol. 2020. PMID: 32654788 Free PMC article. No abstract available.

2

Diagnostic challenge of intrathoracic tissue misplacements: a thymic choristoma in a fetal lung.

Lopez G, Croci R, Rizzuti T, Ferrero S, Fusco N. Lopez G, et al. Among authors: rizzuti t. Thorax. 2019 Jun;74(6):624. doi: 10.1136/thoraxjnl-2019-213242. Epub 2019 Apr 2. Thorax. 2019. PMID: 30940769 No abstract available.

3

High resolution post-mortem MRI of non-fixed in situ foetal brain in the second trimester of gestation: Normal foetal brain development.

Scola E, Conte G, Palumbo G, Avignone S, Cinnante CM, Boito S, Persico N, Rizzuti T, Triulzi F. Scola E, et al. Among authors: rizzuti t. Eur Radiol. 2018 Jan;28(1):363-371. doi: 10.1007/s00330-017-4965-y. Epub 2017 Jul 28. Eur Radiol. 2018. PMID: 28755056

4

Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene.

Gentilin B, Forzano F, Bedeschi MF, Rizzuti T, Faravelli F, Izzi C, Lituania M, Rodriguez-Perez C, Bondioni MP, Savoldi G, Grosso E, Botta G, Viora E, Baffico AM, Lalatta F. Gentilin B, et al. Among authors: rizzuti t. Ultrasound Obstet Gynecol. 2010 Sep;36(3):315-23. doi: 10.1002/uog.7761. Ultrasound Obstet Gynecol. 2010. PMID: 20812307 Free article.

5

SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis.

Fiandrino G, Arossa A, Ghirardello S, Kalantari S, Rossi C, Bonasoni MP, Cesari S, Rizzuti T, Giorgio E, Bassanese F, Scatigno AL, Meroni A, Melito C, Feltri M, Longo S, Figar TA, Andorno A, Gelli MC, Bertozzi M, Spinillo A, Riccipetitoni G, Valente EM, Paulli M, Sirchia F. Fiandrino G, et al. Among authors: rizzuti t. Placenta. 2022 Aug;126:119-124. doi: 10.1016/j.placenta.2022.06.011. Epub 2022 Jun 30. Placenta. 2022. PMID: 35796063

6

An additional piece in the TBX6 gene dosage model: A novel nonsense variant in a fetus with severe spondylocostal dysostosis.

Errichiello E, Arossa A, Iasci A, Villa R, Ischia B, Pavesi MA, Rizzuti T, Bedeschi MF, Zuffardi O. Errichiello E, et al. Among authors: rizzuti t. Clin Genet. 2020 Dec;98(6):628-629. doi: 10.1111/cge.13854. Epub 2020 Oct 14. Clin Genet. 2020. PMID: 33058178 No abstract available.

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: rizzuti t. Prenat Diagn. 2022 Jun;42(7):927-933. doi: 10.1002/pd.6171. Epub 2022 May 27. Prenat Diagn. 2022. PMID: 35584264

8

Norman-Roberts syndrome: characterization of the phenotype in early fetal life.

Natacci F, Bedeschi MF, Righini A, Inverardi F, Rizzuti T, Boschetto C, Triulzi F, Spreafico R, Frassoni C, Lalatta F. Natacci F, et al. Among authors: rizzuti t. Prenat Diagn. 2007 Jun;27(6):568-72. doi: 10.1002/pd.1728. Prenat Diagn. 2007. PMID: 17367103

9

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: rizzuti t. Genet Med. 2018 Nov;20(11):1483-1484. doi: 10.1038/gim.2018.19. Genet Med. 2018. PMID: 29517766 Free article. No abstract available.

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

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