Rozemuller AJ - Search Results

1

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. Among authors: rozemuller aj. J Neuropathol Exp Neurol. 2011 Aug;70(8):698-702. doi: 10.1097/NEN.0b013e3182270c54. J Neuropathol Exp Neurol. 2011. PMID: 21760536

2

[The first patient with the new variant of Creutzfeldt-Jakob's disease in The Netherlands].

Jansen C, Houben MP, Hoff JI, Sanchez-Juan P, Rozemuller AJ, van Duijn CM. Jansen C, et al. Among authors: rozemuller aj. Ned Tijdschr Geneeskd. 2005 Dec 31;149(53):2949-54. Ned Tijdschr Geneeskd. 2005. PMID: 16425845 Dutch.

3

Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patients.

Jansen C, Head MW, Rozemuller AJ, Ironside JW. Jansen C, et al. Among authors: rozemuller aj. Neuropathol Appl Neurobiol. 2009 Jun;35(3):272-82. doi: 10.1111/j.1365-2990.2008.01004a.x. Neuropathol Appl Neurobiol. 2009. PMID: 19473294

4

[Human spongiform encephalopathies in the Netherlands].

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

5

[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. Among authors: rozemuller aj. Ned Tijdschr Geneeskd. 2009;153:A172. Ned Tijdschr Geneeskd. 2009. PMID: 19785859 Dutch.

6

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. Among authors: rozemuller aj. 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.

7

Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology.

Jansen C, van Swieten JC, Capellari S, Strammiello R, Parchi P, Rozemuller AJ. Jansen C, et al. Among authors: rozemuller aj. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1386-9. doi: 10.1136/jnnp.2008.169359. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917818

8

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. Among authors: rozemuller aj. 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.

9

A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.

Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, Wesseling P, Meulstee J, Baas F, van Gool WA, Ironside JW, Rozemuller AJ. Jansen C, et al. Among authors: rozemuller aj. Acta Neuropathol. 2011 Jan;121(1):59-68. doi: 10.1007/s00401-010-0656-3. Epub 2010 Mar 3. Acta Neuropathol. 2011. PMID: 20198483 Free PMC article. Review.

10

The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype.

Jansen C, Head MW, van Gool WA, Baas F, Yull H, Ironside JW, Rozemuller AJ. Jansen C, et al. Among authors: rozemuller aj. J Neurol Neurosurg Psychiatry. 2010 Sep;81(9):1052-5. doi: 10.1136/jnnp.2009.175646. Epub 2010 Jun 14. J Neurol Neurosurg Psychiatry. 2010. PMID: 20547632

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