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Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes.
Brugman F, Scheffer H, Wokke JH, Nillesen WM, de Visser M, Aronica E, Veldink JH, van den Berg LH. Brugman F, et al. Among authors: scheffer h. Neurology. 2008 Nov 4;71(19):1500-5. doi: 10.1212/01.wnl.0000319700.11606.21. Epub 2008 Sep 17. Neurology. 2008. PMID: 18799786
ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes.
de Bot ST, Veldink JH, Vermeer S, Mensenkamp AR, Brugman F, Scheffer H, van den Berg LH, Kremer HP, Kamsteeg EJ, van de Warrenburg BP. de Bot ST, et al. Among authors: scheffer h. J Neurol. 2013 Mar;260(3):869-75. doi: 10.1007/s00415-012-6723-z. Epub 2012 Oct 30. J Neurol. 2013. PMID: 23108492
Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis.
Piepers S, Veldink JH, de Jong SW, van der Tweel I, van der Pol WL, Uijtendaal EV, Schelhaas HJ, Scheffer H, de Visser M, de Jong JM, Wokke JH, Groeneveld GJ, van den Berg LH. Piepers S, et al. Among authors: scheffer h. Ann Neurol. 2009 Aug;66(2):227-34. doi: 10.1002/ana.21620. Ann Neurol. 2009. PMID: 19743466 Clinical Trial.
A natural history study of late onset spinal muscular atrophy types 3b and 4.
Piepers S, van den Berg LH, Brugman F, Scheffer H, Ruiterkamp-Versteeg M, van Engelen BG, Faber CG, de Visser M, van der Pol WL, Wokke JH. Piepers S, et al. Among authors: scheffer h. J Neurol. 2008 Sep;255(9):1400-4. doi: 10.1007/s00415-008-0929-0. Epub 2008 Jun 30. J Neurol. 2008. PMID: 18575920
322 results