Detalhe da pesquisa
1.
Patients' Disalignment in Two Different Healthcare Settings.
Health Commun
; 36(9): 1068-1079, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32204615
2.
Acid sensing ion channel 2: A new potential player in the pathophysiology of multiple sclerosis.
Eur J Neurosci
; 49(10): 1233-1243, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30549327
3.
Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.
Mult Scler
; 24(14): 1815-1824, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28933650
4.
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
Neurogenetics
; 12(3): 203-9, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21667065
5.
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations.
Muscle Nerve
; 44(5): 703-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21953594
6.
Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach.
Front Bioeng Biotechnol
; 8: 397, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32432099
7.
Percutaneous Endoscopic Transgastric Jejunostomy (PEG-J) Tube Placement for Levodopa-Carbidopa Intrajejunal Gel Therapy in the Interventional Radiology Suite: A Long-term Follow-up.
Mov Disord Clin Pract
; 5(2): 191-194, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30363413
8.
Posterior Reversible Encephalopathy Syndrome with Bilateral Independent Epileptic Foci Precipitated By Guillain-Barrè Syndrome.
Case Rep Neurol Med
; 2016: 5913840, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27403359
9.
TBK1 is associated with ALS and ALS-FTD in Sardinian patients.
Neurobiol Aging
; 43: 180.e1-5, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27156075
10.
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry.
Neurobiol Aging
; 36(10): 2906.e1-5, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26208502
11.
A novel LIPE nonsense mutation found using exome sequencing in siblings with late-onset familial partial lipodystrophy.
Can J Cardiol
; 30(12): 1649-54, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25475467
12.
Genetic architecture of ALS in Sardinia.
Neurobiol Aging
; 35(12): 2882.e7-2882.e12, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25123918
13.
Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995-2009.
J Neurol
; 260(2): 572-9, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23052600
14.
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD.
Neurobiol Aging
; 32(12): 2327.e1-5, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21803454
15.
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene.
Arch Neurol
; 68(5): 594-8, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21220647
16.
Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations.
Arch Neurol
; 67(8): 1002-9, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20697052
17.
Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia.
PLoS One
; 4(8): e6526, 2009 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19654877
18.
Partial status epilepticus related to independent occipital foci in posterior reversible encephalopathy syndrome (PRES).
Neurol Sci
; 29(6): 455-8, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19066721
19.
Aquaporin-4 antibody neuromyelitis optica following anti-NMDA receptor encephalitis.
J Neurol
; 260(12): 3185-7, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24253480
20.
Association between the ACCN1 gene and multiple sclerosis in Central East Sardinia.
PLoS One
; 2(5): e480, 2007 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-17534430