Detalhe da pesquisa
1.
Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.
Neurogenetics
; 15(1): 31-40, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24218087
2.
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration.
Neurol Sci
; 33(1): 93-7, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21695656
3.
Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study.
Neurodegener Dis
; 9(3): 121-7, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22123177
4.
Amiodarone increases positive-strand RNA virus replication in vitro: implications for its use in patients with viral infections.
J Antimicrob Chemother
; 71(1): 280-1, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26429565
5.
Protective effects of the combination Bifidobacterium longum plus lactoferrin against NSAID-induced enteropathy.
Nutrition
; 70: 110583, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31739175
6.
A Prospective Evaluation of Two Rapid Phenotypical Antimicrobial Susceptibility Technologies for the Diagnostic Stewardship of Sepsis.
Biomed Res Int
; 2018: 6976923, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29862284
7.
Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139Arg.
Brain Pathol
; 28(1): 72-76, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27997711
8.
Pathophysiology of NSAID-Associated Intestinal Lesions in the Rat: Luminal Bacteria and Mucosal Inflammation as Targets for Prevention.
Front Pharmacol
; 9: 1340, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30555323
9.
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations.
Neurobiol Aging
; 49: 219.e5-219.e13, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27814992
10.
Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing.
Neurobiol Aging
; 40: 192.e7-192.e11, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26925509
11.
Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.
Neurobiol Aging
; 38: 215.e1-215.e12, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26652843
12.
C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.
J Alzheimers Dis
; 38(4): 799-808, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24064469
13.
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
Neurobiol Aging
; 35(2): 408-17, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24018212
14.
Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genome.
J Alzheimers Dis
; 33(4): 969-82, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23047372
15.
New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterization.
Neurobiol Aging
; 33(4): 834.e1-6, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21943955
16.
Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.
PLoS One
; 7(2): e31449, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22363650
17.
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene.
J Alzheimers Dis
; 26(3): 583-90, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21677378
18.
A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expression.
J Alzheimers Dis
; 23(1): 7-12, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20930271
19.
Amiodarone impairs trafficking through late endosomes inducing a Niemann-Pick C-like phenotype.
Biochem Pharmacol
; 82(9): 1234-49, 2011 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21878321
20.
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?
J Neurol Sci
; 359(1-2): 247-9, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26671122