Monia Ginevrino
Overview
Explore the profile of Monia Ginevrino including associated specialties, affiliations and a list of published articles.
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Articles
35
Citations
353
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0
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Recent Articles
1.
David C, Badonyi M, Kechiche R, Insalaco A, Zecca M, De Benedetti F, et al.
J Clin Immunol
. 2024 Feb;
44(2):60.
PMID: 38324161
TLR7 recognizes pathogen-derived single-stranded RNA (ssRNA), a function integral to the innate immune response to viral infection. Notably, TLR7 can also recognize self-derived ssRNA, with gain-of-function mutations in human TLR7...
2.
Moran-Alvarez P, Gianviti A, Diomedi-Camassei F, Ginevrino M, De Benedetti F, Bracaglia C
Pediatr Rheumatol Online J
. 2024 Jan;
22(1):17.
PMID: 38238724
Background: Childhood systemic lupus erythematosus (cSLE) has been considered as a polygenic autoimmune disease; however, a monogenic lupus-like phenotype is emerging with the recent recognition of several related novel high-penetrance...
3.
Nuovo S, Baglioni V, De Mori R, Tardivo S, Caputi C, Ginevrino M, et al.
Hum Mutat
. 2021 Nov;
43(1):67-73.
PMID: 34747546
Biallelic mutations in the BRAT1 gene, encoding BRCA1-associated ATM activator 1, result in variable phenotypes, from rigidity and multifocal seizure syndrome, lethal neonatal to neurodevelopmental disorder, and cerebellar atrophy with...
4.
Fontana P, Ginevrino M, Bejo K, Cantalupo G, Ciavarella M, Lombardi C, et al.
Eur J Med Genet
. 2021 Aug;
64(11):104321.
PMID: 34461323
Several patients with chromosomal deletions including ZFHX4 gene have been described, whereas point mutations are very rare. This gene encodes for a transcription factor involved in the development of several...
5.
Nuovo S, Micalizzi A, Romaniello R, Arrigoni F, Ginevrino M, Casella A, et al.
J Med Genet
. 2021 Jun;
59(4):399-409.
PMID: 34085948
Background: Pontocerebellar hypoplasias (PCH) comprise a group of genetically heterogeneous disorders characterised by concurrent hypoplasia of the pons and the cerebellum and variable clinical and imaging features. The current classification...
6.
Picillo M, Ginevrino M, Dati G, Scannapieco S, Vallelunga A, Siano P, et al.
Parkinsonism Relat Disord
. 2021 Feb;
84:82-90.
PMID: 33601107
Objective: To perform the genetic characterization of a cohort with familial parkinsonism and cognitive-behavioral syndrome. Methods: A Next Generation Sequencing - based targeted sequencing of 32 genes associated to various...
7.
Picillo M, Scannapieco S, Iavarone A, Ginevrino M, Valente E, Barone P
BMC Neurol
. 2021 Jan;
21(1):17.
PMID: 33435912
Background: Glucocerebrosidase (GBA) heterozygous variants are the most important genetic risk factor for the development of alpha-synucleinopathies (i.e., Parkinson's disease and Dementia with Lewy Bodies). Herein, we report for the...
8.
Abate F, Dati G, Ginevrino M, Valente E, Barone P, Picillo M
Mov Disord Clin Pract
. 2020 Oct;
7(7):849-851.
PMID: 33043082
No abstract available.
9.
Guerra A, Asci F, Zampogna A, DOnofrio V, Petrucci S, Ginevrino M, et al.
Clin Neurophysiol
. 2020 Oct;
131(11):2691-2699.
PMID: 33002731
Objective: The main limitation of neuromodulation techniques is inter-subject variability. Combining theta-burst stimulation (TBS) with gamma-transcranial alternating current stimulation (γ-tACS) allows to shape cortical plasticity. However, it is unknown whether...
10.
Heterozygous variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders
Nicita F, Ginevrino M, Travaglini L, DArrigo S, Zorzi G, Borgatti R, et al.
J Med Genet
. 2020 Aug;
58(7):475-483.
PMID: 32737135
Background: Dominant and recessive variants in the gene on chromosome 2q37.3 are associated with several phenotypes, although only three syndromes are currently listed in the OMIM classification: hereditary sensory and...