Alessia Azzarà - Search Results

Year	Number of Results
2013	1
2014	1
2015	1
2016	3
2017	6
2019	3
2020	2
2021	3
2022	5
2023	7
2024	2

1

Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders.

Lintas C, Cassano I, Azzarà A, Stigliano MG, Gregorj C, Sacco R, Stoccoro A, Coppedè F, Gurrieri F. Lintas C, et al. Among authors: azzara a. Genes (Basel). 2023 Feb 25;14(3):585. doi: 10.3390/genes14030585. Genes (Basel). 2023. PMID: 36980856 Free PMC article.

2

Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?

Azzarà A, Cassano I, Lintas C, Pilato F, Capone F, Di Lazzaro V, Gurrieri F. Azzarà A, et al. Genes (Basel). 2023 Jul 20;14(7):1482. doi: 10.3390/genes14071482. Genes (Basel). 2023. PMID: 37510386 Free PMC article.

3

Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations.

Lintas C, Bottillo I, Sacco R, Azzarà A, Cassano I, Ciccone MP, Grammatico P, Gurrieri F. Lintas C, et al. Among authors: azzara a. Genes (Basel). 2022 Dec 1;13(12):2266. doi: 10.3390/genes13122266. Genes (Basel). 2022. PMID: 36553533 Free PMC article.

4

Role of oxidative stress, genome damage and DNA methylation as determinants of pathological conditions in the newborn: an overview from conception to early neonatal stage.

Scarpato R, Testi S, Colosimo V, Garcia Crespo C, Micheli C, Azzarà A, Tozzi MG, Ghirri P. Scarpato R, et al. Among authors: azzara a. Mutat Res Rev Mutat Res. 2020 Jan-Mar;783:108295. doi: 10.1016/j.mrrev.2019.108295. Epub 2019 Dec 26. Mutat Res Rev Mutat Res. 2020. PMID: 32192649 Review.

5

RADX Gene Variant May Predispose to Familial Asperger Syndrome.

Azzarà A, Rumore R, Brugnoletti F, Tabolacci E, Bottillo I, Sangiorgi E, Gurrieri F. Azzarà A, et al. Genes (Basel). 2023 Jan 23;14(2):301. doi: 10.3390/genes14020301. Genes (Basel). 2023. PMID: 36833228 Free PMC article.

6

Genotype-Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results.

Lintas C, Sacco R, Azzarà A, Cassano I, Gurrieri F. Lintas C, et al. Among authors: azzara a. J Clin Med. 2021 Oct 29;10(21):5060. doi: 10.3390/jcm10215060. J Clin Med. 2021. PMID: 34768579 Free PMC article. Review.

7

Vincristine-induced bystander effect in human lymphocytes.

Testi S, Azzarà A, Giovannini C, Lombardi S, Piaggi S, Facioni MS, Scarpato R. Testi S, et al. Among authors: azzara a. Mutat Res. 2016 Jul;789:39-47. doi: 10.1016/j.mrfmmm.2016.03.001. Epub 2016 Mar 25. Mutat Res. 2016. PMID: 27050754

8

Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families.

Azzarà A, Cassano I, Paccagnella E, Tirindelli MC, Nobile C, Schittone V, Lintas C, Sacco R, Gurrieri F. Azzarà A, et al. PLoS One. 2022 Oct 13;17(10):e0275988. doi: 10.1371/journal.pone.0275988. eCollection 2022. PLoS One. 2022. PMID: 36228008 Free PMC article.

9

Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing Study.

Azzarà A, Risi Ambrogioni L, Cassano I, Lintas C, Longo UG, Denaro V, Gurrieri F. Azzarà A, et al. Biology (Basel). 2022 Oct 25;11(11):1565. doi: 10.3390/biology11111565. Biology (Basel). 2022. PMID: 36358266 Free PMC article.

10

Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers.

Sangiorgi E, Azzarà A, Rumore R, Cassano I, Verrecchia E, Giacò L, Tullio MA, Gurrieri F, Manna R. Sangiorgi E, et al. Among authors: azzara a. Genes (Basel). 2023 Jun 21;14(7):1310. doi: 10.3390/genes14071310. Genes (Basel). 2023. PMID: 37510214 Free PMC article.

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