Detalhe da pesquisa
1.
Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis.
Eur J Neurol
; 30(5): 1312-1319, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36746650
2.
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies.
Int J Mol Sci
; 24(4)2023 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36834829
3.
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome.
Hum Mol Genet
; 28(23): 3921-3927, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31600784
4.
Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination.
J Autoimmun
; 124: 102728, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34592707
5.
Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum: the first report.
J Thromb Thrombolysis
; 51(1): 176-179, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32458317
6.
Targeting the Autonomic Nervous System for Risk Stratification, Outcome Prediction and Neuromodulation in Ischemic Stroke.
Int J Mol Sci
; 22(5)2021 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33652990
7.
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG.
BMC Neurol
; 20(1): 316, 2020 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32847536
8.
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy.
Am J Hum Genet
; 97(1): 186-93, 2015 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26094573
9.
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1.
J Neurosci Res
; 96(9): 1576-1585, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30113722
10.
Massive cerebral venous thrombosis due to vaccine-induced immune thrombotic thrombocytopenia.
Haematologica
; 106(11): 3021-3024, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34261296
11.
Expanding the genotypic and phenotypic spectrum of Beta-propeller protein-associated neurodegeneration.
Eur J Neurol
; 28(3): e25-e27, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314449
12.
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.
Brain
; 136(Pt 10): 3119-39, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24030950
13.
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patients.
Pharmacol Res
; 65(4): 472-9, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22306844
14.
New Insights into Cerebral Vessel Disease Landscapes at Single-Cell Resolution: Pathogenetic and Therapeutic Perspectives.
Biomedicines
; 10(7)2022 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35884997
15.
Spinal direct current stimulation (tsDCS) in hereditary spastic paraplegias (HSP): A sham-controlled crossover study.
J Spinal Cord Med
; 44(1): 46-53, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30508408
16.
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study.
Front Neurol
; 12: 729252, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34557155
17.
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?
Intern Emerg Med
; 16(5): 1247-1252, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33565035
18.
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.
Neurogenetics
; 11(1): 91-100, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19593598
19.
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.
J Neurol Neurosurg Psychiatry
; 81(8): 840-3, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20682717
20.
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency.
Ann Clin Transl Neurol
; 7(5): 839-845, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32329585