Maria Alessandra Sotgiu
Overview
Explore the profile of Maria Alessandra Sotgiu 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
17
Citations
243
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
11.
Forte G, Bocca B, Oggiano R, Clemente S, Asara Y, Sotgiu M, et al.
Neurol Sci
. 2017 Jun;
38(9):1609-1615.
PMID: 28601974
Sardinian (Italy) island population has a uniquely high incidence of amyotrophic lateral sclerosis (ALS). Essential trace element levels in blood, hair, and urine of ALS Sardinian patients were investigated in...
12.
DellAvvento S, Sotgiu M, Manca S, Sotgiu G, Sotgiu S
Eur J Pediatr
. 2015 Jul;
175(1):19-29.
PMID: 26156052
Conclusion: Our pMS data among Sardinians corroborate the epidemiological scenario described in the adult population being the incidence estimates significantly higher than those reported elsewhere. What Is Known: Sardinia is...
13.
Mandrile G, Gallus G, Mura G, Di Sapio A, Sotgiu M, Montella A, et al.
Neurol Sci
. 2014 Mar;
35(8):1303-5.
PMID: 24584636
No abstract available.
14.
Chio A, Restagno G, Brunetti M, Ossola I, Calvo A, Canosa A, et al.
J Neurol Neurosurg Psychiatry
. 2012 May;
83(7):730-3.
PMID: 22550220
Background: In the isolated population of Sardinia, a Mediterranean island, ∼25% of ALS cases carry either a p.A382T mutation of the TARDBP gene or a GGGGCC hexanucleotide repeat expansion in...
15.
Sabatelli M, Conforti F, Zollino M, Mora G, Monsurro M, Volanti P, et al.
Neurobiol Aging
. 2012 Mar;
33(8):1848.e15-20.
PMID: 22418734
It has been recently reported that a large proportion of patients with familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are associated with a hexanucleotide (GGGGCC) repeat expansion in...
16.
Chio A, Borghero G, Restagno G, Mora G, Drepper C, Traynor B, et al.
Brain
. 2012 Feb;
135(Pt 3):784-93.
PMID: 22366794
A large hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72, a gene located on chromosome 9p21, has been recently reported to be responsible for ~40% of familial amyotrophic...
17.
Madeddu R, Farace C, Tolu P, Solinas G, Asara Y, Sotgiu M, et al.
Neurol Sci
. 2012 Feb;
34(2):181-6.
PMID: 22362332
The axonal cytoskeleton is a finely organized system, essential for maintaining the integrity of the axon. Axonal degeneration is implicated in the pathogenesis of unremitting disability of multiple sclerosis (MS)....
18.
Sotgiu S, Pugliatti M, Fois M, Arru G, Sanna A, Sotgiu M, et al.
Neurobiol Dis
. 2004 Oct;
17(2):131-43.
PMID: 15474351
Multiple sclerosis (MS) is a chronic disease of the central nervous system affecting young adults and thus representing a major burden also for their families and communities. The etiology of...