Detalhe da pesquisa
1.
Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family.
Mult Scler
; 25(7): 909-917, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29873607
2.
High neurofilament levels are associated with clinically definite multiple sclerosis in children and adults with clinically isolated syndrome.
Mult Scler
; 25(7): 958-967, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29774770
3.
Fatigue after a first attack of suspected multiple sclerosis.
Mult Scler
; 24(7): 974-981, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28532229
4.
Genome-wide significant association with seven novel multiple sclerosis risk loci.
J Med Genet
; 52(12): 848-55, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26475045
5.
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.
Brain
; 136(Pt 6): 1778-82, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23739915
6.
EBNA-1 titer gradient in families with multiple sclerosis indicates a genetic contribution.
Neurol Neuroimmunol Neuroinflamm
; 7(6)2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32796079
7.
Smoking at time of CIS increases the risk of clinically definite multiple sclerosis.
J Neurol
; 265(5): 1010-1015, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29464378
8.
Application of the 2017 Revised McDonald Criteria for Multiple Sclerosis to Patients With a Typical Clinically Isolated Syndrome.
JAMA Neurol
; 75(11): 1392-1398, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30083703
9.
Soluble CD27 Levels in Cerebrospinal Fluid as a Prognostic Biomarker in Clinically Isolated Syndrome.
JAMA Neurol
; 74(3): 286-292, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28055081
10.
Burden of genetic risk variants in multiple sclerosis families in the Netherlands.
Mult Scler J Exp Transl Clin
; 2: 2055217316648721, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-28607725
11.
Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination.
Neurology
; 81(23): 1996-2001, 2013 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24198294
12.
Polymorphisms in CACNA1E and Camk2d are associated with seizure susceptibility of Sprague-Dawley rats.
Epilepsy Res
; 91(1): 28-34, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20638246