Search details
1.
Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.
Ann Neurol
; 89(5): 884-894, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33704824
2.
Antiviral treatment with fluoxetine for rituximab-associated chronic echovirus 13 meningoencephalitis and myofasciitis.
Eur J Neurol
; 29(10): 3117-3123, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35763378
3.
Non-specific symptoms and post-treatment Lyme disease syndrome in patients with Lyme borreliosis: a prospective cohort study in Belgium (2016-2020).
BMC Infect Dis
; 22(1): 756, 2022 Sep 28.
Article
in English
| MEDLINE | ID: mdl-36171561
4.
A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease.
Hum Mol Genet
; 28(8): 1369-1380, 2019 04 15.
Article
in English
| MEDLINE | ID: mdl-30541027
5.
CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity.
Ann Neurol
; 87(4): 633-645, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31997416
6.
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
Brain
; 141(3): 786-796, 2018 03 01.
Article
in English
| MEDLINE | ID: mdl-29361022
7.
Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.
Mult Scler
; 24(13): 1773-1775, 2018 11.
Article
in English
| MEDLINE | ID: mdl-29303040
8.
New insights into the burden and costs of multiple sclerosis in Europe: Results for Belgium.
Mult Scler
; 23(2_suppl): 29-40, 2017 Aug.
Article
in English
| MEDLINE | ID: mdl-28643598
9.
Power estimation for non-standardized multisite studies.
Neuroimage
; 134: 281-294, 2016 07 01.
Article
in English
| MEDLINE | ID: mdl-27039700
10.
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Hum Mol Genet
; 23(7): 1916-22, 2014 Apr 01.
Article
in English
| MEDLINE | ID: mdl-24234648
11.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
Brain
; 138(Pt 3): 632-43, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25616667
12.
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.
Nat Genet
; 39(9): 1083-91, 2007 Sep.
Article
in English
| MEDLINE | ID: mdl-17660817
13.
Burden of risk variants correlates with phenotype of multiple sclerosis.
Mult Scler
; 21(13): 1670-80, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-25948629
14.
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.
Ann Neurol
; 73(1): 86-94, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23225573
15.
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis.
Ann Neurol
; 73(3): 433-7, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23483640
16.
HLA-E restricted CD8+ T cell subsets are phenotypically altered in multiple sclerosis patients.
Mult Scler
; 20(7): 790-801, 2014 06.
Article
in English
| MEDLINE | ID: mdl-24144875
17.
Multiple Sclerosis Multidisciplinary Care: A National Survey and Lessons for the Global Community.
Mult Scler Relat Disord
; 85: 105540, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38489948
18.
Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party.
Blood
; 118(6): 1693-8, 2011 Aug 11.
Article
in English
| MEDLINE | ID: mdl-21596847
19.
Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease.
Mult Scler
; 19(9): 1132-6, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23325590
20.
Optical coherence tomography as a prognostic tool for disability progression in MS: a systematic review.
J Neurol
; 270(2): 1178-1186, 2023 Feb.
Article
in English
| MEDLINE | ID: mdl-36372866