Detalhe da pesquisa
1.
DNA Methylation in the Anti-Mullerian Hormone Gene and the Risk of Disease Activity in Multiple Sclerosis.
Ann Neurol
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747444
2.
Assessment of the genetic contribution to brain magnetic resonance imaging lesion load and atrophy measures in multiple sclerosis patients.
Eur J Neurol
; 28(8): 2513-2522, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864731
3.
A pharmacogenetic study implicates NINJ2 in the response to Interferon-ß in multiple sclerosis.
Mult Scler
; 26(9): 1074-1082, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31221001
4.
Laser capture microdissection for transcriptomic profiles in human skin biopsies.
BMC Mol Biol
; 19(1): 7, 2018 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29921228
5.
NLRP3 polymorphisms and response to interferon-beta in multiple sclerosis patients.
Mult Scler
; 24(11): 1507-1510, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29117789
6.
COL6A5 variants in familial neuropathic chronic itch.
Brain
; 140(3): 555-567, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28073787
7.
A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity.
Ann Neurol
; 78(1): 115-27, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25914168
8.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
Brain
; 138(Pt 3): 632-43, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25616667
9.
Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis.
Mult Scler
; 21(11): 1463-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25533292
10.
The burden of multiple sclerosis variants in continental Italians and Sardinians.
Mult Scler
; 21(11): 1385-95, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26438306
11.
Genetic burden of common variants in progressive and bout-onset multiple sclerosis.
Mult Scler
; 20(7): 802-11, 2014 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24277324
12.
Risk HLA Variants Affect the T-Cell Repertoire in Multiple Sclerosis.
Neurol Neuroimmunol Neuroinflamm
; 10(3)2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36792371
13.
Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach.
J Pers Med
; 13(1)2023 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36675783
14.
Voltage-dependent ionic channels in differentiating neural precursor cells collected from adult mouse brains six hours post-mortem.
J Neurosci Res
; 90(4): 751-8, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22183987
15.
A genome-wide association study in progressive multiple sclerosis.
Mult Scler
; 18(10): 1384-94, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22457343
16.
Transcriptional effects of fingolimod treatment on peripheral T cells in relapsing remitting multiple sclerosis patients.
Pharmacogenomics
; 23(3): 161-171, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35068175
17.
BDNF Val66Met Polymorphism Is Associated With Motor Recovery After Rehabilitation in Progressive Multiple Sclerosis Patients.
Front Neurol
; 13: 790360, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35265024
18.
Involvement of NINJ2 Protein in Inflammation and Blood-Brain Barrier Transmigration of Monocytes in Multiple Sclerosis.
Genes (Basel)
; 13(11)2022 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36360183
19.
Clinical and pathological findings in neurolymphomatosis: Preliminary association with gene expression profiles in sural nerves.
Front Oncol
; 12: 974751, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36226068
20.
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility.
Genes (Basel)
; 13(12)2022 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36553660