Giovanna Marchese
Overview
Explore the profile of Giovanna Marchese including associated specialties, affiliations and a list of published articles.
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Articles
34
Citations
383
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0
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Recent Articles
11.
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...
12.
Salemi M, Lanza G, Mogavero M, Cosentino F, Borgione E, Iorio R, et al.
Int J Mol Sci
. 2022 Feb;
23(3).
PMID: 35163455
Parkinson's disease (PD) is the second most common neurodegenerative disorder. The number of cases of PD is expected to double by 2030, representing a heavy burden on the healthcare system....
13.
Pepe P, Vatrano S, Cannarella R, Calogero A, Marchese G, Ravo M, et al.
Mol Biol Rep
. 2021 Oct;
48(11):7627-7631.
PMID: 34628580
Background: Prostate cancer (PCa) is one of the leading causes of death in Western countries. Environmental and genetic factors play a pivotal role in PCa etiology. Timely identification of the...
14.
Salemi M, Cannarella R, Marchese G, Salluzzo M, Ravo M, Barone C, et al.
Hum Cell
. 2021 Sep;
34(6):1662-1670.
PMID: 34510387
Down syndrome (DS) is defined by the presence of a third copy of chromosome 21. Several comorbidities can be found in these patients, such as intellectual disability (ID), muscle weakness,...
15.
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...
16.
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...
17.
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...
18.
Salemi M, Marchese G, Cordella A, Cannarella R, Barone C, Salluzzo M, et al.
Int J Med Sci
. 2020 Jul;
17(10):1315-1319.
PMID: 32624686
Trisomy 21, also known as Down Syndrome (DS), is the most common chromosome abnormality and causes intellectual disability. Long non-coding RNA (lncRNA) growth arrest-specific 5 (), whose differential expression has...
19.
Pierri L, Saggese P, Guercio Nuzio S, Troisi J, Di Stasi M, Poeta M, et al.
Clin Res Hepatol Gastroenterol
. 2018 May;
42(4):387-390.
PMID: 29773420
No abstract available.
20.
Cimino L, Salemi M, Cannarella R, Condorelli R, Giurato G, Marchese G, et al.
Sci Rep
. 2017 Dec;
7(1):16672.
PMID: 29192217
The widelyvariable phenotypic spectrum and the different severity of symptoms in men with Klinefelter syndrome (KS) suggest a role for epigenetic mediators. Therefore, the aim of this study is to...