Detalhe da pesquisa
1.
Intravenous thrombolysis in CADASIL: report of two cases and a systematic review.
Neurol Sci
; 44(2): 491-498, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36255541
2.
Fabry-Stroke Italian Registry (FSIR): a nationwide, prospective, observational study about incidence and characteristics of Fabry-related stroke in young-adults. Presentation of the study protocol.
Neurol Sci
; 43(4): 2433-2439, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34609660
3.
Constructional Impairments and Their Neural Correlates in Nondemented Adults With Cerebral Autosomal-dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.
Cogn Behav Neurol
; 35(4): 247-254, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36149396
4.
Coverage of the requirements of first and second level stroke unit in Italy.
Neurol Sci
; 42(3): 1073-1079, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32737805
5.
Maternal germline mosaicism in Fabry disease.
Neurol Sci
; 40(6): 1279-1281, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30762167
6.
First report of a homozygous mutation on exon 24 of the NOTCH3 gene in a paucisymptomatic CADASIL elderly patient.
Neurol Sci
; 43(2): 1457-1458, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34739617
7.
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.
Neurol Sci
; 37(6): 875-81, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26850715
8.
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.
Stroke
; 45(4): 968-72, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24578207
9.
Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry.
J Neurol Sci
; 457: 122905, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38295534
10.
Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutation.
Stroke
; 44(4): 1147-9, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23412372
11.
"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation.
Neurol Sci
; 34(11): 1947-53, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23572112
12.
The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale: a screening tool to select patients for NOTCH3 gene analysis.
Stroke
; 43(11): 2871-6, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22996955
13.
Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL).
Neurogenetics
; 12(4): 337-43, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21881852
14.
Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstration.
Clin Neurophysiol
; 119(2): 351-5, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18065265
15.
First report of a Tunisian CADASIL patient.
Neurol Sci
; 34(7): 1239-42, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22955859
16.
CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.
Brain Behav
; 7(3): e00624, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28293466
17.
Cutaneous sensory and autonomic denervation in CADASIL.
Neurology
; 86(11): 1039-44, 2016 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26873958
18.
Cutaneous Sensory and Autonomic Small Fiber Neuropathy in HTRA1-Related Cerebral Small Vessel Disease.
J Neuropathol Exp Neurol
; 80(7): 713-716, 2021 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33313782
19.
APOE É2 is associated with white matter hyperintensity volume in CADASIL.
J Cereb Blood Flow Metab
; 36(1): 199-203, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25920955
20.
CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients.
J Neurol
; 262(1): 134-41, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344745