Detalhe da pesquisa
1.
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study.
J Neurol Neurosurg Psychiatry
; 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38383154
2.
Bilateral Simultaneous Magnetic Resonance-Guided Focused Ultrasound Pallidotomy for Life-Threatening Status Dystonicus.
Mov Disord
; 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641910
3.
Distinct neural signatures of pulvinar in C9orf72 amyotrophic lateral sclerosis mutation carriers and noncarriers.
Eur J Neurol
; 31(6): e16266, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38469975
4.
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia.
Mov Disord
; 38(4): 665-675, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36799493
5.
A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI.
Alzheimers Dement
; 19(8): 3261-3271, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36749840
6.
Subtype Diagnosis of Sporadic Creutzfeldt-Jakob Disease with Diffusion Magnetic Resonance Imaging.
Ann Neurol
; 89(3): 560-572, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33274461
7.
Magnetic Resonance-Guided Focused Ultrasound Thalamotomy May Spare Dopaminergic Therapy in Early-Stage Tremor-Dominant Parkinson's Disease: A Pilot Study.
Mov Disord
; 37(11): 2289-2295, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36036203
8.
Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers.
Cerebellum
; 21(1): 133-144, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34106418
9.
The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy.
Neurol Sci
; 43(6): 3703-3716, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35088242
10.
Pain related to MRgFUS: a merely minor transient adverse event?
J Neurol Neurosurg Psychiatry
; 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641369
11.
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.
Neurol Sci
; 40(3): 561-570, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30604336
12.
Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675.
Int J Mol Sci
; 21(1)2019 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31861461
13.
Letter to the editor: A case of functional isolated tongue tremor-like dyskinesia after COVID-19 vaccine.
Psychiatry Clin Neurosci
; 77(2): 122-123, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36098902
14.
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome.
Int J Mol Sci
; 19(11)2018 11 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30463371
15.
Correction to: The cognitive phenotypes of CreutzfeldtJakob disease: comparison with secondary metabolic encephalopathy.
Neurol Sci
; 43(11): 6609, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35166978
16.
New MAPT variant in a FTD patient with Alzheimer's disease phenotype at onset.
Neurol Sci
; 42(5): 2111-2114, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33201364
17.
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Brain
; 136(Pt 3): 905-17, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23423669
18.
Substantia nigra in Parkinson's disease: a multimodal MRI comparison between early and advanced stages of the disease.
Neurol Sci
; 35(5): 753-8, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24337946
19.
Resting-state fMRI functional connectome of C9orf72 mutation status.
Ann Clin Transl Neurol
; 11(3): 686-697, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38234062
20.
The Optimal Targeting for Focused Ultrasound Thalamotomy Differs between Dystonic and Essential Tremor: A 12-Month Prospective Pilot Study.
Mov Disord Clin Pract
; 11(1): 69-75, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38291839