Detalhe da pesquisa
1.
Familial Alzheimer's disease associated with heterozygous NPC1 mutation.
J Med Genet
; 61(4): 332-339, 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37989569
2.
Clinically relevant increases in serum neurofilament light chain and glial fibrillary acidic protein in patients with Susac syndrome.
Eur J Neurol
; 30(10): 3256-3264, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37335505
3.
Brain neuronal and glial damage during acute COVID-19 infection in absence of clinical neurological manifestations.
J Neurol Neurosurg Psychiatry
; 93(12): 1343-1348, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36137741
4.
Primary familial brain calcification with mild phenotype due to a new PDGFB mutation.
Neurol Sci
; 43(10): 6091-6093, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35750946
5.
Vitamin D in Neurological Diseases.
Int J Mol Sci
; 24(1)2022 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36613531
6.
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia.
Neurol Sci
; 42(12): 5365-5368, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34386887
7.
24S-Hydroxycholesterol and Cerebellar Degeneration: Insights from SCA2.
Cerebellum
; 22(5): 1020-1022, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35851639
8.
Neurofilament light chain and glial fibrillary acid protein levels are elevated in post-mild COVID-19 or asymptomatic SARS-CoV-2 cases.
Sci Rep
; 14(1): 6429, 2024 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38499607
9.
B Lymphocytes in Alzheimer's Disease-A Comprehensive Review.
J Alzheimers Dis
; 88(4): 1241-1262, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35754274
10.
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 gene.
Clin Neurol Neurosurg
; 207: 106763, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34157508