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Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands.
Stunnenberg BC, Raaphorst J, Deenen JCW, Links TP, Wilde AA, Verbove DJ, Kamsteeg EJ, van den Wijngaard A, Faber CG, van der Wilt GJ, van Engelen BGM, Drost G, Ginjaar HB. Stunnenberg BC, et al. Among authors: ginjaar hb. Neuromuscul Disord. 2018 May;28(5):402-407. doi: 10.1016/j.nmd.2018.03.006. Epub 2018 Mar 9. Neuromuscul Disord. 2018. PMID: 29606556
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: ginjaar hb. 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
[From gene to diseases; hypokalemic periodic paralysis].
Links TP, Ginjaar HB, van der Hoeven JH. Links TP, et al. Among authors: ginjaar hb. Ned Tijdschr Geneeskd. 2004 May 22;148(21):1035-8. Ned Tijdschr Geneeskd. 2004. PMID: 15185439 Review. Dutch.
45 results