Angela Cordella
Overview
Explore the profile of Angela Cordella including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
22
Citations
328
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Salemi M, Di Stefano V, Schillaci F, Marchese G, Salluzzo M, Cordella A, et al.
Diagnostics (Basel)
. 2025 Feb;
15(4).
PMID: 40002561
: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by the expansion of the CAG nucleotide repeat in the first exon of the huntingtin () gene. The disease...
2.
Salemi M, Schillaci F, Lanza G, Marchese G, Salluzzo M, Cordella A, et al.
Biomedicines
. 2024 Jul;
12(7).
PMID: 39061976
ASD is a complex condition primarily rooted in genetics, although influenced by environmental, prenatal, and perinatal risk factors, ultimately leading to genetic and epigenetic alterations. These mechanisms may manifest as...
3.
Costantini M, Esposito R, Ruocco N, Caramiello D, Cordella A, Ventola G, et al.
Int J Mol Sci
. 2024 Feb;
25(3).
PMID: 38338963
The Mediterranean purple sea urchin (Lamarck 1816) is a remarkable model system for molecular, evolutionary and cell biology studies, particularly in the field of developmental biology. We sequenced the genome,...
4.
Salemi M, Lanza G, Salluzzo M, Schillaci F, Di Blasi F, Cordella A, et al.
Biomedicines
. 2023 Dec;
11(12).
PMID: 38137339
Parkinson's disease (PD) is a multisystem and multifactorial disorder and, therefore, the application of modern genetic techniques may assist in unraveling its complex pathophysiology. We conducted a clinical-demographic evaluation of...
5.
Salemi M, Mandara L, Salluzzo M, Schillaci F, Castiglione R, Cordella A, et al.
Mol Biol Rep
. 2023 Oct;
50(11):9715-9720.
PMID: 37812352
Background: Gerstmann Sträussler Scheinker (GSS) is an inherited, invariably fatal prion disease. Like other human prion diseases, GSS is caused by missense mutations in the prion protein (PrP) gene (PRNP),...
6.
Salemi M, Marchese G, Lanza G, Cosentino F, Salluzzo M, Schillaci F, et al.
Int J Mol Sci
. 2023 Jan;
24(1).
PMID: 36614153
Parkinson's disease (PD) is a neurodegenerative synucleinopathy that has a not yet fully understood molecular pathomechanism behind it. The role of risk genes regulated by small non-coding RNAs, or microRNAs...
7.
Salemi M, Cannarella R, Marchese G, Salluzzo M, Ravo M, Barone C, et al.
Mol Biol Rep
. 2021 Jun;
48(6):5335-5338.
PMID: 34184200
Chromosome 21 trisomy or Down syndrome (DS) is the most common genetic cause of intellectual disability (ID). DS is also associated with hypotonia, muscle weakness, autoimmune diseases, and congenital heart...
8.
Salemi M, Cannarella R, Cimino L, Condorelli R, Giurato G, Marchese G, et al.
Minerva Endocrinol (Torino)
. 2020 Dec;
46(4):384-388.
PMID: 33331742
Background: The etiology of azoospermia in patients with Klinefelter Syndrome (KS) is still unknown. The protein codified by the G protein-couple receptor 56 (GPR56) belongs to the adhesion family of...
9.
Gentile M, Ranieri C, Loconte D, Ponzi E, Ficarella R, Volpe P, et al.
Clin Genet
. 2020 Nov;
99(3):425-429.
PMID: 33236357
mTOR dysregulation has been described in pathological conditions, such as cardiovascular and overgrowth disorders. Here we report on the first case of a patient with a complex congenital heart disease...
10.
Cannarella R, Salemi M, Condorelli R, Cimino L, Giurato G, Marchese G, et al.
Asian J Androl
. 2020 Oct;
23(2):157-162.
PMID: 33109779
Klinefelter syndrome (KS) is the most common sex chromosome disorder in men. It is characterized by germ cell loss and other variable clinical features, including autoimmunity. The sex-determining region of...