Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Maria Grazia Salluzzo"'
Autor:
Maria P. Mogavero, Michele Salemi, Giuseppe Lanza, Antonio Rinaldi, Giovanna Marchese, Maria Ravo, Maria Grazia Salluzzo, Amedeo Antoci, Lourdes M. DelRosso, Oliviero Bruni, Luigi Ferini-Strambi, Raffaele Ferri
Publikováno v:
iScience, Vol 27, Iss 4, Pp 109568- (2024)
Summary: The aim of this study was to analyze signaling pathways associated with differentially expressed messenger RNAs in people with restless legs syndrome (RLS). Seventeen RLS patients and 18 controls were enrolled. Coding RNA expression profilin
Externí odkaz:
https://doaj.org/article/d016dab7cce84c0c8114e7ed975040eb
Autor:
Michele Salemi, Francesca A. Schillaci, Giuseppe Lanza, Giovanna Marchese, Maria Grazia Salluzzo, Angela Cordella, Salvatore Caniglia, Maria Grazia Bruccheri, Anna Truda, Donatella Greco, Raffaele Ferri, Corrado Romano
Publikováno v:
Biomedicines, Vol 12, Iss 7, p 1402 (2024)
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 inflammatory, oxidative st
Externí odkaz:
https://doaj.org/article/3bc02b36d093489b8790b79eaf40386c
Autor:
Gisella M. Di Mari, Mario Scuderi, Giuseppe Lanza, Maria Grazia Salluzzo, Michele Salemi, Filippo Caraci, Elena Bruno, Vincenzina Strano, Salvo Mirabella, Antonino Scandurra
Publikováno v:
Nanomaterials, Vol 14, Iss 2, p 170 (2024)
Analytical methods for the early detection of the neurodegenerative biomarker for Parkinson’s disease (PD), α-synuclein, are time-consuming and invasive, and require skilled personnel and sophisticated and expensive equipment. Thus, a pain-free, p
Externí odkaz:
https://doaj.org/article/12306b48c27943d68d36eb98165f8f5c
Autor:
Michele Salemi, Giuseppe Lanza, Maria Grazia Salluzzo, Francesca A. Schillaci, Francesco Domenico Di Blasi, Angela Cordella, Salvatore Caniglia, Bartolo Lanuzza, Manuela Morreale, Pietro Marano, Mariangela Tripodi, Raffaele Ferri
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3118 (2023)
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 126 patient
Externí odkaz:
https://doaj.org/article/893d101c178f4f3fa6ef37daefda1f4d
Autor:
Michele Salemi, Filomena Cosentino, Giuseppe Lanza, Mariagiovanna Cantone, Maria Grazia Salluzzo, Giorgio Giurato, Eugenia Borgione, Giovanna Marchese, Sandro Santa Paola, Bartolo Lanuzza, Corrado Romano, Raffaele Ferri
Publikováno v:
Archives of Medical Science, Vol 19, Iss 3, Pp 678-686 (2021)
Introduction Parkinson’s disease (PD) is a common adult-onset neurodegenerative disorder caused by a progressive loss of dopaminergic neurons due to the accumulation of α-synuclein in the substantia nigra. Mitochondria are known to play a key role
Externí odkaz:
https://doaj.org/article/e7728c5ae8434c2f9d8469dd775aaa7d
Autor:
Michele Salemi, Federico Ridolfo, Maria Grazia Salluzzo, Francesca A. Schillaci, Salvatore Caniglia, Bartolo Lanuzza, Mariagiovanna Cantone, Raffaele Ferri
Publikováno v:
Molecular Biology Reports. 50:2943-2949
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13f11aa77002c08dfe54a96312a3e096
https://doi.org/10.1007/s11033-022-08132-3
https://doi.org/10.1007/s11033-022-08132-3
Autor:
Michele Salemi, Giovanna Marchese, Giuseppe Lanza, Filomena I. I. Cosentino, Maria Grazia Salluzzo, Francesca A. Schillaci, Giovanna Maria Ventola, Angela Cordella, Maria Ravo, Raffaele Ferri
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 1; Pages: 712
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 (miRNAs), has also been highlighted in P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f29adcc836561b3b2d3c93a421cd67
https://hdl.handle.net/20.500.11769/550425
https://hdl.handle.net/20.500.11769/550425
Autor:
Michele Salemi, Giuseppe Lanza, Maria Paola Mogavero, Filomena I. I. Cosentino, Eugenia Borgione, Roberta Iorio, Giovanna Maria Ventola, Giovanna Marchese, Maria Grazia Salluzzo, Maria Ravo, Raffaele Ferri
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1535
International Journal of Molecular Sciences, Vol 23, Iss 1535, p 1535 (2022)
International Journal of Molecular Sciences, Vol 23, Iss 1535, p 1535 (2022)
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. Clinical symptoms include the progressive loss of dopamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48ba0352df7195bef0393ded999ac91
http://hdl.handle.net/20.500.11769/521965
http://hdl.handle.net/20.500.11769/521965
Autor:
Corrado Romano, Aldo E. Calogero, Concetta Barone, Maria Grazia Salluzzo, Giovanna Marchese, Rossella Cannarella, Maria Ravo, Michele Salemi, Mariangela Lo Giudice
Publikováno v:
Human cell. 34(6)
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, hypotonia, congenital heart disease, and autoimmune diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b9ec4f52eafb7489c36c822b42d9677
https://pubmed.ncbi.nlm.nih.gov/34510387
https://pubmed.ncbi.nlm.nih.gov/34510387
Autor:
Roberto Castiglione, Salvatore Caniglia, Michele Salemi, Corrado Romano, Maria Grazia Salluzzo, Giovanna Marchese, Aldo E. Calogero, Rossella Cannarella, Alda Ragalmuto, Maria Ravo, Concetta Barone, Angela Cordella
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 disease. C-C chemokine receptor type 3 (CCR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577ce18d4b22ecb26d3a34ea89dfef63
http://hdl.handle.net/20.500.11769/524365
http://hdl.handle.net/20.500.11769/524365