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'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation.
Boissé Lomax L, Bayly MA, Hjalgrim H, Møller RS, Vlaar AM, Aaberg KM, Marquardt I, Gandolfo LC, Willemsen M, Kamsteeg EJ, O'Sullivan JD, Korenke GC, Bloem BR, de Coo IF, Verhagen JM, Said I, Prescott T, Stray-Pedersen A, Rasmussen M, Vears DF, Lehesjoki AE, Corbett MA, Bahlo M, Gecz J, Dibbens LM, Berkovic SF. Boissé Lomax L, et al. Among authors: willemsen m. Brain. 2013 Apr;136(Pt 4):1146-54. doi: 10.1093/brain/awt021. Epub 2013 Feb 28. Brain. 2013. PMID: 23449775
Prospective assessment of falls in Parkinson's disease.
Bloem BR, Grimbergen YA, Cramer M, Willemsen M, Zwinderman AH. Bloem BR, et al. Among authors: willemsen m. J Neurol. 2001 Nov;248(11):950-8. doi: 10.1007/s004150170047. J Neurol. 2001. PMID: 11757958
The Multiple Tasks Test: development and normal strategies.
Bloem BR, Valkenburg VV, Slabbekoorn M, Willemsen MD. Bloem BR, et al. Among authors: willemsen md. Gait Posture. 2001 Dec;14(3):191-202. doi: 10.1016/s0966-6362(01)00141-2. Gait Posture. 2001. PMID: 11600322
OTULIN haploinsufficiency predisposes to environmentally directed inflammation.
Staels F, Bücken L, De Vuyst L, Willemsen M, Van Nieuwenhove E, Gerbaux M, Neumann J, Malviya V, Van Meerbeeck L, Haughton J, Seldeslachts L, Gouwy M, Martinod K, Vande Velde G, Proost P, Yshii L, Schlenner S, Schrijvers R, Liston A, Humblet-Baron S. Staels F, et al. Among authors: willemsen m. Front Immunol. 2024 May 21;15:983686. doi: 10.3389/fimmu.2024.983686. eCollection 2024. Front Immunol. 2024. PMID: 38827742 Free PMC article.
Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals.
Dingemans AJM, Jansen S, van Reeuwijk J, de Leeuw N, Pfundt R, Schuurs-Hoeijmakers J, van Bon BW, Marcelis C, Ockeloen CW, Willemsen M, van der Sluijs PJ, Santen GWE, Kooy RF, Vulto-van Silfhout AT, Kleefstra T, Koolen DA, Vissers LELM, de Vries BBA. Dingemans AJM, et al. Among authors: willemsen m. Nat Med. 2024 May 14. doi: 10.1038/s41591-024-03005-7. Online ahead of print. Nat Med. 2024. PMID: 38745008
Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants.
Wortmann SB, Feichtinger RG, Abela L, van Gemert LA, Aubart M, Dufeu-Berat CM, Boddaert N, de Coo R, Stühn L, Hebbink J, Heinritz W, Hildebrandt J, Himmelreich N, Korenke C, Lehman A, Leyland T, Makowski C, Martinez Marin RJ, Marzin P, Mühlhausen C, Rio M, Rotig A, Roux CJ, Schiff M, Haack TB, Syrbe S, Zylicz SA, Thiel C, Veiga da Cunha M, van Schaftingen E, Wagner M, Mayr JA, Wevers RA, Boltshauser E, Willemsen MA. Wortmann SB, et al. Among authors: willemsen ma. Neurol Genet. 2024 Apr 5;10(2):e200146. doi: 10.1212/NXG.0000000000200146. eCollection 2024 Apr. Neurol Genet. 2024. PMID: 38617198 Free PMC article.
640 results