Detalhe da pesquisa
1.
MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy.
Neurol Sci
; 43(10): 6117-6120, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35690699
2.
Characteristics and outcomes of cerebral venous thrombosis associated with COVID-19.
Eur Stroke J
; : 23969873241241885, 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38572798
3.
Cytotoxic lesions of the corpus callosum during the course of ketotic hyperglycemia revealing type I diabetes: A case report.
SAGE Open Med Case Rep
; 11: 2050313X231172338, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37187493
4.
Intravascular large cell B lymphoma presenting as central nervous system pseudo-vasculitis: A rare diagnostic challenge.
Neuroradiol J
; : 19714009231212351, 2023 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37933603
5.
Neurological involvement in SARS-CoV-2 infection: A clinical systematic review.
Brain Behav Immun Health
; 5: 100094, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33521692
6.
p.Gly743Val Mutation in COL4A1 Is Responsible for Familial Porencephaly and Severe Hypermetropia.
Front Neurol
; 11: 827, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33013618
7.
Multimodal imaging for a TIPIC syndrome case.
Acta Neurol Belg
; 122(4): 1069-1071, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486716
8.
Headache, Bilateral Carotid Stenosis, and Hypoglossal Palsy Revealing Granulomatosis with Polyangiitis: An Innovative Application of Vessel-Wall MRI.
J Clin Neurol
; 17(1): 137-139, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33480211
9.
Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene.
J Neurol
; 260(4): 1116-21, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23196337