Bruson A - Search Results

1

Reply to the Letter - "The development of Brugada syndrome phenotype is multifactorial, combining genetic and environmental factors".

Maltese PE, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli M. Maltese PE, et al. Among authors: bruson a. Eur Rev Med Pharmacol Sci. 2020 Apr;24(7):3446-3447. doi: 10.26355/eurrev_202004_20800. Eur Rev Med Pharmacol Sci. 2020. PMID: 32329816 Free article. No abstract available.

2

Putative role of Brugada syndrome genes in familial atrial fibrillation.

Maltese PE, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli M. Maltese PE, et al. Among authors: bruson a. Eur Rev Med Pharmacol Sci. 2019 Sep;23(17):7582-7598. doi: 10.26355/eurrev_201909_18880. Eur Rev Med Pharmacol Sci. 2019. PMID: 31539150 Free article.

3

Vascular anomalies: molecular bases, genetic testing and therapeutic approaches.

Paolacci S, Zulian A, Bruson A, Manara E, Michelini S, Mattassi RE, Lee BB, Amato B, Bertelli M. Paolacci S, et al. Among authors: bruson a. Int Angiol. 2019 Apr;38(2):157-170. doi: 10.23736/S0392-9590.19.04154-3. Epub 2019 Apr 1. Int Angiol. 2019. PMID: 30938497 Free article. Review.

4

Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.

Maltese PE, Michelini S, Ricci M, Maitz S, Fiorentino A, Serrani R, Lazzerotti A, Bruson A, Paolacci S, Benedetti S, Bertelli M. Maltese PE, et al. Among authors: bruson a. Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18. Am J Med Genet A. 2019. PMID: 31215153

5

Variant discovery in patients with Mendelian vascular anomalies by next-generation sequencing and their use in patient clinical management.

Mattassi R, Manara E, Colombo PG, Manara S, Porcella A, Bruno G, Bruson A, Bertelli M. Mattassi R, et al. Among authors: bruson a. J Vasc Surg. 2018 Mar;67(3):922-932.e11. doi: 10.1016/j.jvs.2017.02.034. Epub 2017 Jun 24. J Vasc Surg. 2018. PMID: 28655553 Free article.

6

Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.

Michelini S, Vettori A, Maltese PE, Cardone M, Bruson A, Fiorentino A, Cappellino F, Sainato V, Guerri G, Marceddu G, Tezzele S, Bertelli M. Michelini S, et al. Among authors: bruson a. Lymphology. 2016 Jun;49(2):57-72. Lymphology. 2016. PMID: 29906362

7

Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy.

Iarossi G, Bertelli M, Maltese PE, Gusson E, Marchini G, Bruson A, Benedetti S, Volpetti S, Catena G, Buzzonetti L, Ziccardi L. Iarossi G, et al. Among authors: bruson a. J Ophthalmol. 2017;2017:3080245. doi: 10.1155/2017/3080245. Epub 2017 Jul 5. J Ophthalmol. 2017. PMID: 28758032 Free PMC article.

8

Corrigendum to "Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy".

Iarossi G, Bertelli M, Maltese PE, Gusson E, Marchini G, Bruson A, Benedetti S, Volpetti S, Catena G, Buzzonetti L, Ziccardi L. Iarossi G, et al. Among authors: bruson a. J Ophthalmol. 2017;2017:7969364. doi: 10.1155/2017/7969364. Epub 2017 Nov 30. J Ophthalmol. 2017. PMID: 29333293 Free PMC article.

9

A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene.

Michelini S, Cardone M, Haag M, Agga O, Bruson A, Maltese PE, Bonizzato A, Bertelli M. Michelini S, et al. Among authors: bruson a. Lymphology. 2016 Mar;49(1):15-20. Lymphology. 2016. PMID: 29906059

10

Is CFTR 621+3 A>G a cystic fibrosis causing mutation?

Forzan M, Salviati L, Pertegato V, Casarin A, Bruson A, Trevisson E, Di Gianantonio E, Clementi M. Forzan M, et al. Among authors: bruson a. J Hum Genet. 2010 Jan;55(1):23-6. doi: 10.1038/jhg.2009.115. Epub 2009 Nov 6. J Hum Genet. 2010. PMID: 19893581

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