Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gaia Citterio"'
Autor:
Letizia Corinna Morlacchi, Gianfranco Alicandro, Sara Uceda Renteria, Nunzio Zignani, Giovanni Giacomel, Valeria Rossetti, Michele Sagasta, Gaia Citterio, Andrea Lombardi, Clara Dibenedetto, Barbara Antonelli, Lorenzo Rosso, Pietro Lampertico, Ferruccio Ceriotti, Francesco Blasi, Maria Francesca Donato
Publikováno v:
Transplant International, Vol 37 (2024)
This study assessed humoral and T cell-mediated immune responses to the BNT162b2 vaccine in orthotopic liver transplant (OLT) and lung transplant (LUT) recipients who received three doses of the vaccine from March 2021 at our institution. Serum sampl
Externí odkaz:
https://doaj.org/article/3eed1a63e1c14d2f933350818295bc51
Publikováno v:
Neurobiology of Disease, Vol 140, Iss , Pp 104870- (2020)
Spinal muscular atrophy (SMA) is a severe, inherited disease characterized by the progressive degeneration and death of motor neurons of the anterior horns of the spinal cord, which results in muscular atrophy and weakness of variable severity. Its e
Externí odkaz:
https://doaj.org/article/03e1e58c91ec4b4ea2982632424356ea
Autor:
Elena Abati, Monica Sciacco, Eleonora Mauri, Eleonora Piccin, Luca Andreoli, Luigia Scudeller, Nereo Bresolin, Megi Meneri, Stefania Corti, Roberta Brusa, Delia Gagliardi, Gaia Citterio, Francesca Magri, Daniele Velardo, Gianluca Costamagna, Giacomo P. Comi
Publikováno v:
Muscle & Nerve
Introduction:/Aims Patients with neuromuscular disorders (NMDs), including many elderly, immunosuppressed, and disabled individuals, may have been particularly affected during the coronavirus disease 2019 (COVID‐19) pandemic in Lombardy, a COVID‐
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6f168dd716033f1374214ab5e5223f
https://doi.org/10.1002/mus.27378
https://doi.org/10.1002/mus.27378
Autor:
Giacomo P. Comi, Monica Nizzardo, Roberta De Gioia, Stefania Corti, Gaia Citterio, Elena Abati, Federica Rizzo, Nereo Bresolin
Publikováno v:
Molecular Neurobiology
Charcot–Marie–Tooth disease type 2A (CMT2A), arising from mitofusin 2 (MFN2) gene mutations, is the most common inherited axonal neuropathy affecting motor and sensory neurons. The cellular and molecular mechanisms by whichMFN2mutations determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06a53b5592a2a93fd02926f4f256d35e
http://europepmc.org/articles/PMC7541381
http://europepmc.org/articles/PMC7541381
Autor:
Gaia Citterio, Roberta De Gioia, Giacomo P. Comi, Monica Nizzardo, Elena Abati, Federica Rizzo, Nereo Bresolin, Stefania Corti, Fabio Biella
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 3103, p 3103 (2020)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Neurodegenerative diseases are disabling and fatal neurological disorders that currently lack effective treatment. Neural stem cell (NSC) transplantation has been studied as a potential therapeutic approach and appears to exert a beneficial effect ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc3a7cc3646b05bd7952afddd2f64ad9
https://www.mdpi.com/1422-0067/21/9/3103
https://www.mdpi.com/1422-0067/21/9/3103