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Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.
Zaharieva IT, Thor MG, Oates EC, van Karnebeek C, Hendson G, Blom E, Witting N, Rasmussen M, Gabbett MT, Ravenscroft G, Sframeli M, Suetterlin K, Sarkozy A, D'Argenzio L, Hartley L, Matthews E, Pitt M, Vissing J, Ballegaard M, Krarup C, Slørdahl A, Halvorsen H, Ye XC, Zhang LH, Løkken N, Werlauff U, Abdelsayed M, Davis MR, Feng L, Phadke R, Sewry CA, Morgan JE, Laing NG, Vallance H, Ruben P, Hanna MG, Lewis S, Kamsteeg EJ, Männikkö R, Muntoni F. Zaharieva IT, et al. Among authors: krarup c. Brain. 2016 Mar;139(Pt 3):674-91. doi: 10.1093/brain/awv352. Epub 2015 Dec 22. Brain. 2016. PMID: 26700687 Free PMC article.
Motor axon excitability during Wallerian degeneration.
Moldovan M, Alvarez S, Krarup C. Moldovan M, et al. Among authors: krarup c. Brain. 2009 Feb;132(Pt 2):511-23. doi: 10.1093/brain/awn332. Epub 2008 Dec 11. Brain. 2009. PMID: 19074190
Diagnosis of acute neuropathies.
Crone C, Krarup C. Crone C, et al. Among authors: krarup c. J Neurol. 2007 Sep;254(9):1151-69. doi: 10.1007/s00415-007-0532-9. Epub 2007 Sep 21. J Neurol. 2007. PMID: 18000737 Review.
129 results