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Maaike M van der Graaff

Explore the profile of Maaike M van der Graaff including associated specialties, affiliations and a list of published articles. Areas
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Articles 5
Citations 181
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Recent Articles
1.
Walgaard C, Jacobs B, Lingsma H, Steyerberg E, van den Berg B, Doets A, et al.
Lancet Neurol . 2021 Mar; 20(4):275-283. PMID: 33743237
Background: Treatment with one standard dose (2 g/kg) of intravenous immunoglobulin is insufficient in a proportion of patients with severe Guillain-Barré syndrome. Worldwide, around 25% of patients severely affected with...
2.
van der Graaff M, Sage C, Caan M, Akkerman E, Lavini C, Majoie C, et al.
Brain . 2011 Mar; 134(Pt 4):1211-28. PMID: 21362631
Motoneuron disease is a term encompassing three phenotypes defined largely by the balance of upper versus lower motoneuron involvement, namely amyotrophic lateral sclerosis, primary lateral sclerosis and progressive muscular atrophy....
3.
Caan M, van Vliet L, Majoie C, van der Graaff M, Grimbergen C, Vos F
IEEE Trans Biomed Eng . 2010 Dec; 58(9):2431-40. PMID: 21118765
Patient studies based on diffusion tensor images (DTI) require spatial correspondence between subjects. We propose to obtain the correspondence from white matter tracts, by introducing a new method for nonrigid...
4.
van der Graaff M, Grolman W, Westermann E, Boogaardt H, Koelman H, van der Kooi A, et al.
Arch Neurol . 2009 Nov; 66(11):1329-33. PMID: 19901163
We describe 4 patients with amyotrophic lateral sclerosis (ALS) and glottic narrowing due to vocal cord dysfunction, and review the literature found using the following search terms: amyotrophic lateral sclerosis,...
5.
Meredith C, Herrmann R, Parry C, Liyanage K, Dye D, Durling H, et al.
Am J Hum Genet . 2004 Aug; 75(4):703-8. PMID: 15322983
We previously linked Laing-type early-onset autosomal dominant distal myopathy (MPD1) to a 22-cM region of chromosome 14. One candidate gene in the region, MYH7, which is mutated in cardiomyopathy and...