Search details
1.
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation.
Eur J Neurol
; 27(12): 2630-2634, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32894632
2.
Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola Disease.
Cytokine
; 116: 115-119, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30690291
3.
Repetitive element hypermethylation in multiple sclerosis patients.
BMC Genet
; 17(1): 84, 2016 06 18.
Article
in English
| MEDLINE | ID: mdl-27317098
4.
Inflammatory molecules in Frontotemporal Dementia: cerebrospinal fluid signature of progranulin mutation carriers.
Brain Behav Immun
; 49: 182-7, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26021560
5.
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study.
Mult Scler
; 21(8): 1013-24, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25680984
6.
Binge eating and fast cognitive worsening in an early-onset bvFTD patient carrying C9ORF72 expansion.
Neurocase
; 21(5): 543-7, 2015.
Article
in English
| MEDLINE | ID: mdl-25158292
7.
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.
Mol Biol Evol
; 29(6): 1599-613, 2012 Jun.
Article
in English
| MEDLINE | ID: mdl-22319148
8.
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect.
Geroscience
; 45(3): 1557-1571, 2023 06.
Article
in English
| MEDLINE | ID: mdl-36725819
9.
Salivary proteomic profile of young healthy subjects.
Front Mol Biosci
; 10: 1327233, 2023.
Article
in English
| MEDLINE | ID: mdl-38099196
10.
Response of renal parenchyma and interstitium of Rana snk. esculenta to environmental pollution.
Ecotoxicol Environ Saf
; 74(5): 1381-90, 2011 Jul.
Article
in English
| MEDLINE | ID: mdl-21497903
11.
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.
Genes Immun
; 11(6): 497-503, 2010 Sep.
Article
in English
| MEDLINE | ID: mdl-20463744
12.
The CST3 B haplotype is associated with frontotemporal lobar degeneration.
Eur J Neurol
; 17(1): 143-6, 2010 Jan.
Article
in English
| MEDLINE | ID: mdl-19674067
13.
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort.
Eur J Neurol
; 17(5): 740-5, 2010 May.
Article
in English
| MEDLINE | ID: mdl-20067515
14.
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Eur J Neurol
; 16(1): 37-42, 2009 Jan.
Article
in English
| MEDLINE | ID: mdl-19087148
15.
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
Eur J Neurol
; 16(7): 870-3, 2009 Jul.
Article
in English
| MEDLINE | ID: mdl-19473369
16.
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration.
Rejuvenation Res
; 11(4): 773-80, 2008 Aug.
Article
in English
| MEDLINE | ID: mdl-18729809
17.
The functional MAOA-uVNTR promoter polymorphism in patients with frontotemporal dementia.
Eur J Neurol
; 15(6): 637-9, 2008 Jun.
Article
in English
| MEDLINE | ID: mdl-18474080
18.
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
Eur J Neurol
; 15(1): 77-81, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-18042235
19.
Novel exon 1 progranulin gene variant in Alzheimer's disease.
Eur J Neurol
; 15(10): 1111-7, 2008 Oct.
Article
in English
| MEDLINE | ID: mdl-18752597
20.
A histochemical approach to the evaluation of the in vivo cytotoxicity of the nitrobutadienes (1E,3E)-1,4-bis(1-naphthyl)-2,3-dinitro-1,3-butadiene and methyl (2Z,4E)-2-methylsulfanyl-5-(1-naphthyl)-4-nitro-2,4-pentadienoate in mice liver and kidney.
Anticancer Res
; 28(2A): 813-23, 2008.
Article
in English
| MEDLINE | ID: mdl-18507024