Ellen Corsmit
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Explore the profile of Ellen Corsmit including associated specialties, affiliations and a list of published articles.
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997
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Recent Articles
1.
Barbe B, Corsmit E, Jans J, Kaur K, Baets R, Jacobs J, et al.
Diagnostics (Basel)
. 2022 Mar;
12(3).
PMID: 35328168
Bloodstream infections and antimicrobial resistance are an increasing problem in low-income countries. There is a clear need for adapted diagnostic tools. To address this need, we developed a simple, universal...
2.
Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, et al.
Neurology
. 2014 Oct;
83(21):1906-13.
PMID: 25326098
Objectives: The objective of this study is to clarify the role of (G4C2)n expansions in the etiology of Parkinson disease (PD) in the worldwide multicenter Genetic Epidemiology of Parkinson's Disease...
3.
Sieben A, Danek A, Martin J, Vandenberghe R, De Deyn P, Corsmit E, et al.
Hum Mutat
. 2012 Nov;
34(2):363-73.
PMID: 23111906
We assessed the geographical distribution of C9orf72 G(4) C(2) expansions in a pan-European frontotemporal lobar degeneration (FTLD) cohort (n = 1,205), ascertained by the European Early-Onset Dementia (EOD) consortium. Next,...
4.
Theuns J, Crosiers D, Debaene L, Nuytemans K, Meeus B, Sleegers K, et al.
Mov Disord
. 2012 Sep;
27(11):1451-6.
PMID: 22976901
Background: Autosomal dominant dopa-responsive dystonia (AD-DRD) is caused by a biochemical defect primarily resulting from guanosine triphosphate cyclohydrolase 1 gene (GCH1) mutations. Few families have been reported without mutations in...
5.
Verstraeten A, Wauters E, Crosiers D, Meeus B, Corsmit E, Elinck E, et al.
Neurobiol Aging
. 2012 Feb;
33(8):1844.e11-3.
PMID: 22336192
VPS35 was recently identified as a novel autosomal dominant gene for Parkinson disease. In this study, we aimed to determine the contribution of simple and complex VPS35 variations to the...
6.
Gijselinck I, Van Langenhove T, van der Zee J, Sleegers K, Philtjens S, Kleinberger G, et al.
Lancet Neurol
. 2011 Dec;
11(1):54-65.
PMID: 22154785
Background: Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are extremes of a clinically, pathologically, and genetically overlapping disease spectrum. A locus on chromosome 9p21 has been associated with...
7.
Meeus B, Verstraeten A, Crosiers D, Engelborghs S, Van den Broeck M, Mattheijssens M, et al.
Neurobiol Aging
. 2011 Nov;
33(3):629.e5-629.e18.
PMID: 22118943
Based on the substantial overlap in clinical and pathological characteristics of dementia with Lewy bodies (DLB) and Parkinson disease with dementia (PDD) with Alzheimer disease (AD) and Parkinson disease (PD)...
8.
Comprehensive genetic and mutation analysis of familial dementia with Lewy bodies linked to 2q35-q36
Meeus B, Nuytemans K, Crosiers D, Engelborghs S, Peeters K, Mattheijssens M, et al.
J Alzheimers Dis
. 2010 Feb;
20(1):197-205.
PMID: 20164589
The second most frequent form of neurodegenerative dementia after Alzheimer's disease is dementia with Lewy bodies (DLB). Since informative DLB families are scarce, little is presently known about the molecular...
9.
Nuytemans K, Meeus B, Crosiers D, Brouwers N, Goossens D, Engelborghs S, et al.
Hum Mutat
. 2009 May;
30(7):1054-61.
PMID: 19405094
The relative contribution of simple mutations and copy number variations (CNVs) in SNCA, PARK2, PINK1, PARK7, and LRRK2 to the genetic etiology of Parkinson disease (PD) is still unclear because...
10.
Meeus B, Nuytemans K, Crosiers D, Engelborghs S, Pals P, Pickut B, et al.
Neurobiol Aging
. 2009 Mar;
32(2):308-12.
PMID: 19321232
Missense mutations were identified in the Grb10-Interacting GYF Protein-2 gene (GIGYF2), located in the chromosomal region 2q36-q37, in familial Parkinson disease (PD) patients of European descent. To determine the contribution...