Maria Brigida Lioi - Search Results

Year	Number of Results
2005	1
2008	2
2009	1
2011	2
2012	3
2013	4
2014	2
2015	1
2019	4
2021	1
2022	4
2024	0

1

Radiofrequency Electromagnetic Field Exposure and Apoptosis: A Scoping Review of In Vitro Studies on Mammalian Cells.

Romeo S, Zeni O, Scarfì MR, Poeta L, Lioi MB, Sannino A. Romeo S, et al. Among authors: lioi mb. Int J Mol Sci. 2022 Feb 19;23(4):2322. doi: 10.3390/ijms23042322. Int J Mol Sci. 2022. PMID: 35216437 Free PMC article. Review.

2

Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male.

Pescatore A, Spinosa E, Casale C, Lioi MB, Ursini MV, Fusco F. Pescatore A, et al. Among authors: lioi mb. Int J Mol Sci. 2022 Jan 21;23(3):1179. doi: 10.3390/ijms23031179. Int J Mol Sci. 2022. PMID: 35163099 Free PMC article. Review.

3

Clinical utility gene card: for incontinentia pigmenti.

Fusco F, Pescatore A, Steffann J, Bonnefont JP, De Oliveira J, Lioi MB, Ursini MV. Fusco F, et al. Among authors: lioi mb. Eur J Hum Genet. 2019 Dec;27(12):1894-1900. doi: 10.1038/s41431-019-0463-9. Epub 2019 Jul 9. Eur J Hum Genet. 2019. PMID: 31289372 Free PMC article. No abstract available.

4

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Poeta L, Malacarne M, Padula A, Drongitis D, Verrillo L, Lioi MB, Chiariello AM, Bianco S, Nicodemi M, Piccione M, Salzano E, Coviello D, Miano MG. Poeta L, et al. Among authors: lioi mb. Int J Mol Sci. 2022 Mar 13;23(6):3084. doi: 10.3390/ijms23063084. Int J Mol Sci. 2022. PMID: 35328505 Free PMC article. Review.

5

EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammation.

Fusco F, Pescatore A, Conte MI, Mirabelli P, Paciolla M, Esposito E, Lioi MB, Ursini MV. Fusco F, et al. Among authors: lioi mb. Int Rev Immunol. 2015;34(6):445-59. doi: 10.3109/08830185.2015.1055331. Epub 2015 Aug 13. Int Rev Immunol. 2015. PMID: 26269396 Review.

6

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Drongitis D, Caterino M, Verrillo L, Santonicola P, Costanzo M, Poeta L, Attianese B, Barra A, Terrone G, Lioi MB, Paladino S, Di Schiavi E, Costa V, Ruoppolo M, Miano MG. Drongitis D, et al. Among authors: lioi mb. Hum Mol Genet. 2022 Jun 4;31(11):1884-1908. doi: 10.1093/hmg/ddac028. Hum Mol Genet. 2022. PMID: 35094084 Free PMC article.

7

Treatment with 3-Aminobenzamide Negates the Radiofrequency-Induced Adaptive Response in Two Cell Models.

Sannino A, Zeni O, Romeo S, Lioi MB, Scarfì MR. Sannino A, et al. Among authors: lioi mb. Int J Environ Res Public Health. 2019 Aug 2;16(15):2768. doi: 10.3390/ijerph16152768. Int J Environ Res Public Health. 2019. PMID: 31382475 Free PMC article.

8

Incontinentia pigmenti: report on data from 2000 to 2013.

Fusco F, Paciolla M, Conte MI, Pescatore A, Esposito E, Mirabelli P, Lioi MB, Ursini MV. Fusco F, et al. Among authors: lioi mb. Orphanet J Rare Dis. 2014 Jun 24;9:93. doi: 10.1186/1750-1172-9-93. Orphanet J Rare Dis. 2014. PMID: 24961275 Free PMC article.

9

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Poeta L, Padula A, Lioi MB, van Bokhoven H, Miano MG. Poeta L, et al. Among authors: lioi mb. Genes (Basel). 2021 Jul 18;12(7):1088. doi: 10.3390/genes12071088. Genes (Basel). 2021. PMID: 34356104 Free PMC article.

10

The Incontinentia Pigmenti Genetic Biobank: study design and cohort profile to facilitate research into a rare disease worldwide.

Fusco F, Valente V, Fergola D, Pescatore A, Lioi MB, Ursini MV. Fusco F, et al. Among authors: lioi mb. Eur J Hum Genet. 2019 Oct;27(10):1509-1518. doi: 10.1038/s41431-019-0451-0. Epub 2019 Jun 23. Eur J Hum Genet. 2019. PMID: 31231133 Free PMC article.

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