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260 results

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Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD).
Goselink RJ, Schreuder TH, Mul K, Voermans NC, Pelsma M, de Groot IJ, van Alfen N, Franck B, Theelen T, Lemmers RJ, Mah JK, van der Maarel SM, van Engelen BG, Erasmus CE. Goselink RJ, et al. Among authors: voermans nc. BMC Neurol. 2016 Aug 17;16:138. doi: 10.1186/s12883-016-0664-6. BMC Neurol. 2016. PMID: 27530735 Free PMC article. Clinical Trial.
Adding quantitative muscle MRI to the FSHD clinical trial toolbox.
Mul K, Vincenten SCC, Voermans NC, Lemmers RJLF, van der Vliet PJ, van der Maarel SM, Padberg GW, Horlings CGC, van Engelen BGM. Mul K, et al. Among authors: voermans nc. Neurology. 2017 Nov 14;89(20):2057-2065. doi: 10.1212/WNL.0000000000004647. Epub 2017 Oct 13. Neurology. 2017. PMID: 29030457 Free PMC article.
A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1.
Wohlgemuth M, Lemmers RJ, Jonker M, van der Kooi E, Horlings CG, van Engelen BG, van der Maarel SM, Padberg GW, Voermans NC. Wohlgemuth M, et al. Among authors: voermans nc. Neurology. 2018 Jul 31;91(5):e444-e454. doi: 10.1212/WNL.0000000000005915. Epub 2018 Jul 11. Neurology. 2018. PMID: 29997197 Free PMC article.
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1.
Mul K, Voermans NC, Lemmers RJLF, Jonker MA, van der Vliet PJ, Padberg GW, van Engelen BGM, van der Maarel SM, Horlings CGC. Mul K, et al. Among authors: voermans nc. Clin Genet. 2018 Dec;94(6):521-527. doi: 10.1111/cge.13446. Epub 2018 Oct 8. Clin Genet. 2018. PMID: 30211448
260 results