Brugman F - Search Results

1

Spastin mutations in sporadic adult-onset upper motor neuron syndromes.

Brugman F, Wokke JH, Scheffer H, Versteeg MH, Sistermans EA, van den Berg LH. Brugman F, et al. Ann Neurol. 2005 Dec;58(6):865-9. doi: 10.1002/ana.20652. Ann Neurol. 2005. PMID: 16240363

2

Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes.

Brugman F, Scheffer H, Schelhaas HJ, Nillesen WM, Wokke JH, van de Warrenburg BP, van den Berg LH. Brugman F, et al. J Neurol. 2009 May;256(5):824-6. doi: 10.1007/s00415-009-5009-6. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252810 No abstract available.

3

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.

Brugman F, Veldink JH, Franssen H, de Visser M, de Jong JM, Faber CG, Kremer BH, Schelhaas HJ, van Doorn PA, Verschuuren JJ, Bruyn RP, Kuks JB, Robberecht W, Wokke JH, van den Berg LH. Brugman F, et al. Arch Neurol. 2009 Apr;66(4):509-14. doi: 10.1001/archneurol.2009.19. Arch Neurol. 2009. PMID: 19364936

4

Primary lateral sclerosis as a phenotypic manifestation of familial ALS.

Brugman F, Wokke JH, Vianney de Jong JM, Franssen H, Faber CG, Van den Berg LH. Brugman F, et al. Neurology. 2005 May 24;64(10):1778-9. doi: 10.1212/01.WNL.0000162033.47893.F7. Neurology. 2005. PMID: 15911810

5

Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene.

Brugman F, Eymard-Pierre E, van den Berg LH, Wokke JH, Gauthier-Barichard F, Boespflug-Tanguy O. Brugman F, et al. Neurology. 2007 Aug 14;69(7):702-4. doi: 10.1212/01.wnl.0000267322.48364.76. Neurology. 2007. PMID: 17698795 No abstract available.

6

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: brugman f. J Neurol. 2008 Sep;255(9):1400-4. doi: 10.1007/s00415-008-0929-0. Epub 2008 Jun 30. J Neurol. 2008. PMID: 18575920

7

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. Neurology. 2008 Nov 4;71(19):1500-5. doi: 10.1212/01.wnl.0000319700.11606.21. Epub 2008 Sep 17. Neurology. 2008. PMID: 18799786

8

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: brugman f. J Neurol. 2013 Mar;260(3):869-75. doi: 10.1007/s00415-012-6723-z. Epub 2012 Oct 30. J Neurol. 2013. PMID: 23108492

9

Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging study.

van der Graaff MM, Sage CA, Caan MW, Akkerman EM, Lavini C, Majoie CB, Nederveen AJ, Zwinderman AH, Vos F, Brugman F, van den Berg LH, de Rijk MC, van Doorn PA, Van Hecke W, Peeters RR, Robberecht W, Sunaert S, de Visser M. van der Graaff MM, et al. Among authors: brugman f. Brain. 2011 Apr;134(Pt 4):1211-28. doi: 10.1093/brain/awr016. Epub 2011 Feb 28. Brain. 2011. PMID: 21362631

10

MR spectroscopy findings in early stages of motor neuron disease.

van der Graaff MM, Lavini C, Akkerman EM, Majoie ChB, Nederveen AJ, Zwinderman AH, Brugman F, van den Berg LH, de Jong JM, de Visser M. van der Graaff MM, et al. Among authors: brugman f. AJNR Am J Neuroradiol. 2010 Nov;31(10):1799-806. doi: 10.3174/ajnr.A2217. Epub 2010 Aug 26. AJNR Am J Neuroradiol. 2010. PMID: 20801763 Free PMC article. Clinical Trial.

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