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Treatment of Guillain-Barré syndrome with mycophenolate mofetil: a pilot study.
Garssen MP, van Koningsveld R, van Doorn PA, Merkies IS, Scheltens-de Boer M, van Leusden JA, van Schaik IN, Linssen WH, Visscher F, Boon AM, Faber CG, Meulstee J, Prick MJ, van den Berg LH, Franssen H, Hiel JA, van den Bergh PY, Sindic CJ. Garssen MP, et al. Among authors: faber cg. J Neurol Neurosurg Psychiatry. 2007 Sep;78(9):1012-3. doi: 10.1136/jnnp.2006.102731. J Neurol Neurosurg Psychiatry. 2007. PMID: 17702789 Free PMC article. Clinical Trial. No abstract available.
Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.
Trip J, Drost G, Ginjaar HB, Nieman FH, van der Kooi AJ, de Visser M, van Engelen BG, Faber CG. Trip J, et al. Among authors: faber cg. J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):647-52. doi: 10.1136/jnnp.2008.162396. Epub 2009 Feb 11. J Neurol Neurosurg Psychiatry. 2009. PMID: 19211598
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
240 results