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Activities of daily living in myotonic dystrophy type 1.
Landfeldt E, Nikolenko N, Jimenez-Moreno C, Cumming S, Monckton DG, Faber CG, Merkies ISJ, Gorman G, Turner C, Lochmüller H. Landfeldt E, et al. Among authors: faber cg. Acta Neurol Scand. 2020 May;141(5):380-387. doi: 10.1111/ane.13215. Epub 2020 Jan 21. Acta Neurol Scand. 2020. PMID: 31889295 Free article.
Intraepidermal nerve fiber density and its application in sarcoidosis.
Bakkers M, Merkies IS, Lauria G, Devigili G, Penza P, Lombardi R, Hermans MC, van Nes SI, De Baets M, Faber CG. Bakkers M, et al. Among authors: faber cg. Neurology. 2009 Oct 6;73(14):1142-8. doi: 10.1212/WNL.0b013e3181bacf05. Neurology. 2009. PMID: 19805731 Free article.
Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
Braida C, Stefanatos RK, Adam B, Mahajan N, Smeets HJ, Niel F, Goizet C, Arveiler B, Koenig M, Lagier-Tourenne C, Mandel JL, Faber CG, de Die-Smulders CE, Spaans F, Monckton DG. Braida C, et al. Among authors: faber cg. Hum Mol Genet. 2010 Apr 15;19(8):1399-412. doi: 10.1093/hmg/ddq015. Epub 2010 Jan 15. Hum Mol Genet. 2010. PMID: 20080938
Hereditary muscular dystrophies and the heart.
Hermans MC, Pinto YM, Merkies IS, de Die-Smulders CE, Crijns HJ, Faber CG. Hermans MC, et al. Among authors: faber cg. Neuromuscul Disord. 2010 Aug;20(8):479-92. doi: 10.1016/j.nmd.2010.04.008. Neuromuscul Disord. 2010. PMID: 20627570 Review.
252 results