Rozemuller AJM - Search Results

1

Three VCP Mutations in Patients with Frontotemporal Dementia.

Wong TH, Pottier C, Hondius DC, Meeter LHH, van Rooij JGJ, Melhem S; Netherlands Brain bank; van Minkelen R, van Duijn CM, Rozemuller AJM, Seelaar H, Rademakers R, van Swieten JC. Wong TH, et al. Among authors: rozemuller ajm. J Alzheimers Dis. 2018;65(4):1139-1146. doi: 10.3233/JAD-180301. J Alzheimers Dis. 2018. PMID: 30103325

2

Nrf2-induced antioxidant protection: a promising target to counteract ROS-mediated damage in neurodegenerative disease?

de Vries HE, Witte M, Hondius D, Rozemuller AJ, Drukarch B, Hoozemans J, van Horssen J. de Vries HE, et al. Free Radic Biol Med. 2008 Nov 15;45(10):1375-83. doi: 10.1016/j.freeradbiomed.2008.09.001. Epub 2008 Sep 13. Free Radic Biol Med. 2008. PMID: 18824091 Review.

3

[Human spongiform encephalopathies in the Netherlands].

Schuur M, Jansen C, Rozemuller AJ, van Gool WA, van Duijn CM. Schuur M, et al. Ned Tijdschr Geneeskd. 2009;153:A173. Ned Tijdschr Geneeskd. 2009. PMID: 19785856 Review. Dutch.

4

[Eleven years of autopsy on account of Creutzfeldt-Jakob disease in the Netherlands].

Jansen C, Schuur M, Spliet WG, van Gool WA, van Duijn CM, Rozemuller AJ. Jansen C, et al. Ned Tijdschr Geneeskd. 2009;153:A172. Ned Tijdschr Geneeskd. 2009. PMID: 19785859 Dutch.

5

Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

Jansen C, Parchi P, Capellari S, Vermeij AJ, Corrado P, Baas F, Strammiello R, van Gool WA, van Swieten JC, Rozemuller AJ. Jansen C, et al. Acta Neuropathol. 2010 Feb;119(2):189-97. doi: 10.1007/s00401-009-0609-x. Epub 2009 Nov 13. Acta Neuropathol. 2010. PMID: 19911184 Free PMC article.

6

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration.

Seelaar H, Klijnsma KY, de Koning I, van der Lugt A, Chiu WZ, Azmani A, Rozemuller AJ, van Swieten JC. Seelaar H, et al. J Neurol. 2010 May;257(5):747-53. doi: 10.1007/s00415-009-5404-z. Epub 2009 Nov 28. J Neurol. 2010. PMID: 19946779 Free PMC article.

7

Brain perfusion patterns in familial frontotemporal lobar degeneration.

Seelaar H, Papma JM, Garraux G, de Koning I, Reijs AE, Valkema R, Rozemuller AJ, Salmon E, van Swieten JC. Seelaar H, et al. Neurology. 2011 Jul 26;77(4):384-92. doi: 10.1212/WNL.0b013e3182270456. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753175

8

A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.

Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ. Jansen C, et al. J Neuropathol Exp Neurol. 2011 Aug;70(8):698-702. doi: 10.1097/NEN.0b013e3182270c54. J Neuropathol Exp Neurol. 2011. PMID: 21760536

9

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

Dopper EG, Seelaar H, Chiu WZ, de Koning I, van Minkelen R, Baker MC, Rozemuller AJ, Rademakers R, van Swieten JC. Dopper EG, et al. J Mol Neurosci. 2011 Nov;45(3):354-8. doi: 10.1007/s12031-011-9626-z. Epub 2011 Aug 24. J Mol Neurosci. 2011. PMID: 21863316 Free PMC article.

10

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

Simón-Sánchez J, Dopper EG, Cohn-Hokke PE, Hukema RK, Nicolaou N, Seelaar H, de Graaf JR, de Koning I, van Schoor NM, Deeg DJ, Smits M, Raaphorst J, van den Berg LH, Schelhaas HJ, De Die-Smulders CE, Majoor-Krakauer D, Rozemuller AJ, Willemsen R, Pijnenburg YA, Heutink P, van Swieten JC. Simón-Sánchez J, et al. Brain. 2012 Mar;135(Pt 3):723-35. doi: 10.1093/brain/awr353. Epub 2012 Feb 1. Brain. 2012. PMID: 22300876

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