Stefania Corti
Overview
Explore the profile of Stefania Corti including associated specialties, affiliations and a list of published articles.
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Articles
263
Citations
5330
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Recent Articles
1.
Lucchiari S, Magri F, Rimoldi M, Pagliarani S, Corti S, Comi G, et al.
Acta Myol
. 2025 Feb;
43(4):134-138.
PMID: 40017289
Objective: Myotonic dystrophy type 2 (DM2; PROMM) is characterized by myotonia and muscle dysfunction, episodic muscle pain, proximal and axial weakness of the neck flexors. We describe the case of...
2.
Cappelletti G, Brambilla L, Strizzi S, Limanaqi F, Melzi V, Rizzuti M, et al.
FASEB J
. 2025 Feb;
39(4):e70396.
PMID: 39950320
COVID-19 commonly leads to respiratory issues, yet numerous patients also exhibit a diverse range of neurological conditions, suggesting a detrimental impact of SARS-CoV-2 or the viral Spike protein on the...
3.
Corti S, Sansone V, Bitetti I, Brolatti N, Gadaleta G, Patanella A, et al.
Neuromuscul Disord
. 2025 Feb;
48:105278.
PMID: 39908680
The landscape of spinal muscular atrophy care is evolving with the emergence of disease-modifying therapies and newborn screening programs, leading to new phenotypes and changing patient needs. This necessitates a...
4.
5.
Pagliari E, Taiana M, Manzini P, Sali L, Quetti L, Bertolasi L, et al.
Cell Mol Life Sci
. 2024 Dec;
82(1):29.
PMID: 39725771
The development of ground-breaking Survival Motor Neuron (SMN) replacement strategies has revolutionized the field of Spinal Muscular Atrophy (SMA) research. However, the limitations of these therapies have now become evident,...
6.
Lucchiari S, Fortunato F, Meola G, Mignarri A, Pagliarani S, Corti S, et al.
Front Genet
. 2024 Dec;
15:1486977.
PMID: 39712484
Myotonia congenita, both in a dominant (Thomsen disease) and recessive form (Becker disease), is caused by molecular defects in that encodes the major skeletal muscle chloride channel, ClC-1. This channel...
7.
Abati E, Alberti C, Tambe V, Esseridou A, Comi G, Corti S, et al.
Front Neurol
. 2024 Dec;
15:1493570.
PMID: 39639989
Introduction: Non-invasive evaluation of myocardial tissue is a major goal of cardiac imaging. This is the case of myocardial fibrosis which is crucial in many myocardial diseases. Cardiac extracellular volume...
8.
Alberti C, Molitierno N, Iacobelli V, Velardo D, Comi G, Corti S, et al.
Ther Adv Neurol Disord
. 2024 Dec;
17:17562864241297086.
PMID: 39628849
Guillain-Barré syndrome (GBS) and its variants represent a spectrum of acute, immune-mediated polyneuropathies with heterogeneous clinical presentations and underlying etiologies. While infectious triggers are common precursors to these disorders, the...
9.
Frattini E, Faustini G, Lopez G, Carsana E, Tosi M, Trezzi I, et al.
Brain
. 2024 Nov;
PMID: 39570889
Fibrillary aggregation of α-synuclein in Lewy body inclusions and nigrostriatal dopaminergic neuron degeneration define Parkinson's disease neuropathology. Mutations in GBA1, encoding glucocerebrosidase, are the most frequent genetic risk factor for...
10.
Saez-Atienzar S, Souza C, Chia R, Beal S, Lorenzini I, Huang R, et al.
Cell Genom
. 2024 Oct;
4(11):100679.
PMID: 39437787
Repeat expansions in the C9orf72 gene are the most common genetic cause of (ALS) and frontotemporal dementia (FTD). Like other genetic forms of neurodegeneration, pinpointing the precise mechanism(s) by which...