Girolamo Aurelio Vitello
Overview
Explore the profile of Girolamo Aurelio Vitello including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
63
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Recent Articles
1.
Ceraolo G, Spoto G, Butera A, Spano M, Vinci M, Vitello G, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2024 Oct;
198(3):e33015.
PMID: 39440920
TRMT10A is related to a syndrome characterized by early-onset diabetes mellitus, microcephaly, epilepsy, and intellectual disability. We report a case of a patient showing spastic-ataxic paraparesis and Dandy-Walker variant associated...
2.
Musumeci A, Vinci M, Verbinnen I, Treccarichi S, Nigliato E, Chiavetta V, et al.
Gene
. 2024 Sep;
933:148945.
PMID: 39284558
Protein phosphatase 2A (PP2A) is a family of multifunctional enzymatic complexes crucial for cellular signalling, playing a pivotal role in brain function and development. Mutations in specific genes encoding PP2A...
3.
Cali F, Vinci M, Treccarichi S, Papa C, Gloria A, Musumeci A, et al.
Genes (Basel)
. 2024 Aug;
15(8).
PMID: 39202455
Hypoxic-ischemic brain damage presents a significant neurological challenge, often manifesting during the perinatal period. Specifically, periventricular leukomalacia (PVL) is emerging as a notable contributor to cerebral palsy and intellectual disabilities....
4.
Vinci M, Vitello G, Greco D, Treccarichi S, Ragalmuto A, Musumeci A, et al.
Curr Issues Mol Biol
. 2024 Feb;
46(2):1150-1163.
PMID: 38392191
Ion channelopathies result from impaired ion channel protein function, due to mutations affecting ion transport across cell membranes. Over 40 diseases, including neuropathy, pain, migraine, epilepsy, and ataxia, are associated...
5.
Pennisi M, Lanza G, Vitello G, Faro D, Fisicaro F, Cappellani F, et al.
Life (Basel)
. 2023 Dec;
13(12).
PMID: 38137907
Background: Clinically, there is considerable heterogeneity in the presentation of transthyretin amyloidosis (ATTR), which ranges from primarily cardiac and primarily neurologic to mixed disease, among other manifestations. Because of this...
6.
Butera A, Nicotera A, Di Rosa G, Musumeci S, Vitello G, Musumeci A, et al.
Int J Mol Sci
. 2022 Dec;
23(24).
PMID: 36555772
() gene, located in the short arm of chromosome 11, encodes for BHC80, a component of the Lysine Specific Demethylase 1, Corepressor of REST (LSD1-CoREST) complex. BHC80 is mainly expressed...
7.
Musumeci A, Cali F, Scuderi C, Vinci M, Vitello G, Musumeci S, et al.
Biomedicines
. 2022 Sep;
10(9).
PMID: 36140376
Recessive mutations in the POLR3A gene cause POLR3-HLD (the second-most-common form of childhood-onset hypomyelinating leukodystrophy), a neurodegenerative disorder featuring deficient cerebral myelin formation. To date, more than 140 POLR3A (NM_007055.3)...
8.
Vitello G, Federico C, Bruno F, Vinci M, Musumeci A, Ragalmuto A, et al.
Int J Mol Sci
. 2022 Aug;
23(16).
PMID: 36012436
During the first wave of COVID-19 infection in Italy, the number of cases and the mortality rates were among the highest compared to the rest of Europe and the world....
9.
Nicotera A, Di Rosa G, Turriziani L, Costanzo M, Stracuzzi E, Vitello G, et al.
Brain Sci
. 2021 Oct;
11(10).
PMID: 34679357
Antipsychotics (APDs) represent the main pharmacological strategy in the treatment of schizophrenia; however, their administration often may result in severe adverse effects, such as extrapyramidal symptoms. Typically, dystonic movements are...
10.
Vetri L, Elia M, Vitello G, Greco D, Gagliano C, Costanzo M, et al.
Perspect Psychiatr Care
. 2021 May;
57(3):1536-1537.
PMID: 34032288
No abstract available.