Graziano C - Search Results

1

Coronary Artery Aneurysms in Patients With Marfan Syndrome: Frequent, Progressive, and Relevant.

Mariucci E, Bonori L, Lovato L, Graziano C, Ciuca C, Pacini D, Di Marco L, Angeli E, Careddu L, Gargiulo G, Donti A. Mariucci E, et al. Among authors: graziano c. Can J Cardiol. 2021 Aug;37(8):1225-1231. doi: 10.1016/j.cjca.2021.03.002. Epub 2021 Mar 9. Can J Cardiol. 2021. PMID: 33711475

2

High prevalence of arterial dissection in patients with Loeys-Dietz syndrome and cerebral aneurysm.

Spinardi L, Mariucci E, Vornetti G, Stagni S, Graziano C, Faccioli L, Pastore Trossello M, Donti A. Spinardi L, et al. Among authors: graziano c. Vasc Med. 2020 Jun;25(3):218-220. doi: 10.1177/1358863X19900923. Epub 2020 Mar 4. Vasc Med. 2020. PMID: 32129152 No abstract available.

3

Aortic arch geometry predicts outcome in patients with Loeys-Dietz syndrome independent of the causative gene.

Mariucci E, Spinardi L, Stagni S, Graziano C, Lovato L, Pacini D, Di Marco L, Careddu L, Angeli E, Ciuca C, Wischmeijer A, Gargiulo G, Donti A. Mariucci E, et al. Among authors: graziano c. Am J Med Genet A. 2020 Jul;182(7):1673-1680. doi: 10.1002/ajmg.a.61608. Epub 2020 Apr 30. Am J Med Genet A. 2020. PMID: 32352226

4

Intracranial Arterial Tortuosity in Marfan Syndrome and Loeys-Dietz Syndrome: Tortuosity Index Evaluation Is Useful in the Differential Diagnosis.

Spinardi L, Vornetti G, De Martino S, Golfieri R, Faccioli L, Pastore Trossello M, Graziano C, Mariucci E, Donti A. Spinardi L, et al. Among authors: graziano c. AJNR Am J Neuroradiol. 2020 Oct;41(10):1916-1922. doi: 10.3174/ajnr.A6732. Epub 2020 Aug 20. AJNR Am J Neuroradiol. 2020. PMID: 32819908 Free PMC article.

5

Increased intracranial arterial tortuosity is associated with worse cardiovascular outcome in patients with Loeys-Dietz syndrome.

Vornetti G, Spinardi L, Mariucci E, Graziano C, Baroni MC, Faccioli L, Donti A. Vornetti G, et al. Among authors: graziano c. J Clin Neurosci. 2022 Feb;96:38-42. doi: 10.1016/j.jocn.2021.12.020. Epub 2021 Dec 30. J Clin Neurosci. 2022. PMID: 34974246

6

MR Brain Screening in ADPKD Patients : To Screen or not to Screen?

Capelli I, Zoli M, Righini M, Faccioli L, Aiello V, Spinardi L, Gori D, Friso F, Rustici A, Bortolotti C, Graziano C, Mantovani V, Sciascia N, Mazzatenta D, Seri M, Pastore Trossello M, La Manna G. Capelli I, et al. Among authors: graziano c. Clin Neuroradiol. 2022 Mar;32(1):69-78. doi: 10.1007/s00062-021-01050-0. Epub 2021 Sep 29. Clin Neuroradiol. 2022. PMID: 34586427 Free PMC article.

7

Chromosomal Microarray Analysis Identifies a Novel SALL1 Deletion, Supporting the Association of Haploinsufficiency with a Mild Phenotype of Townes-Brocks Syndrome.

Innoceta AM, Olivucci G, Parmeggiani G, Scarano E, Pragliola A, Graziano C. Innoceta AM, et al. Among authors: graziano c. Genes (Basel). 2023 Jan 19;14(2):258. doi: 10.3390/genes14020258. Genes (Basel). 2023. PMID: 36833185 Free PMC article. Review.

8

There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss.

Morgan A, Faletra F, Severi G, La Bianca M, Licchetta L, Gasparini P, Graziano C, Girotto G. Morgan A, et al. Among authors: graziano c. Biomedicines. 2021 Dec 22;10(1):12. doi: 10.3390/biomedicines10010012. Biomedicines. 2021. PMID: 35052694 Free PMC article.

9

New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer.

Severi G, Bernardini L, Briuglia S, Bigoni S, Buldrini B, Magini P, Dentici ML, Cordelli DM, Arrigo T, Franzoni E, Fini S, Italyankina E, Loddo I, Novelli A, Graziano C. Severi G, et al. Among authors: graziano c. Am J Med Genet A. 2016 Jan;170A(1):162-9. doi: 10.1002/ajmg.a.37346. Epub 2015 Sep 3. Am J Med Genet A. 2016. PMID: 26333654

10

A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature.

Graziano C, Gusson E, Severi G, Isidori F, Wischmeijer A, Brugnara M, Seri M, Rossi C. Graziano C, et al. Ophthalmic Genet. 2017 Dec;38(6):590-592. doi: 10.1080/13816810.2017.1318927. Epub 2017 May 4. Ophthalmic Genet. 2017. PMID: 28471317 No abstract available.

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