Brandel JP - Search Results

1

V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation.

Chasseigneaux S, Haïk S, Laffont-Proust I, De Marco O, Lenne M, Brandel JP, Hauw JJ, Laplanche JL, Peoc'h K. Chasseigneaux S, et al. Among authors: brandel jp. Neurosci Lett. 2006 Nov 20;408(3):165-9. doi: 10.1016/j.neulet.2006.08.008. Epub 2006 Oct 9. Neurosci Lett. 2006. PMID: 17029785

2

Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998.

D'Aignaux JH, Cousens SN, Delasnerie-Lauprêtre N, Brandel JP, Salomon D, Laplanche JL, Hauw JJ, Alpérovitch A. D'Aignaux JH, et al. Among authors: brandel jp. Int J Epidemiol. 2002 Apr;31(2):490-5. Int J Epidemiol. 2002. PMID: 11980824

3

Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK.

Brandel JP, Preece M, Brown P, Croes E, Laplanche JL, Agid Y, Will R, Alpérovitch A. Brandel JP, et al. Lancet. 2003 Jul 12;362(9378):128-30. doi: 10.1016/S0140-6736(03)13867-6. Lancet. 2003. PMID: 12867116

4

Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.

Haïk S, Peoc'h K, Brandel JP, Privat N, Laplanche JL, Faucheux BA, Hauw JJ. Haïk S, et al. Among authors: brandel jp. Ann Neurol. 2004 Dec;56(6):909-10; author reply 910-1. doi: 10.1002/ana.20327. Ann Neurol. 2004. PMID: 15562434 No abstract available.

5

Differentiation of sCJD and vCJD forms by automated analysis of basal ganglia intensity distribution in multisequence MRI of the brain--definition and evaluation of new MRI-based ratios.

Linguraru MG, Ayache N, Bardinet E, Ballester MA, Galanaud D, Haïk S, Faucheux B, Hauw JJ, Cozzone P, Dormont D, Brandel JP. Linguraru MG, et al. Among authors: brandel jp. IEEE Trans Med Imaging. 2006 Aug;25(8):1052-67. doi: 10.1109/tmi.2006.876133. IEEE Trans Med Imaging. 2006. PMID: 16894998

6

In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.

Haïk S, Galanaud D, Linguraru MG, Peoc'h K, Privat N, Faucheux BA, Ayache N, Hauw JJ, Dormont D, Brandel JP. Haïk S, et al. Among authors: brandel jp. Arch Neurol. 2008 Apr;65(4):545-9. doi: 10.1001/archneur.65.4.545. Arch Neurol. 2008. PMID: 18413481

7

Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.

Levavasseur E, Laffont-Proust I, Morain E, Faucheux BA, Privat N, Peoc'h K, Sazdovitch V, Brandel JP, Hauw JJ, Haïk S. Levavasseur E, et al. Among authors: brandel jp. PLoS One. 2008 Jul 30;3(7):e2786. doi: 10.1371/journal.pone.0002786. PLoS One. 2008. PMID: 18665216 Free PMC article.

8

[Creutzfeldt-Jakob disease in patients before and after 80 years of age].

Brandel JP, Salomon D, Hauw JJ, Haïk S, Alpérovitch A. Brandel JP, et al. Psychol Neuropsychiatr Vieil. 2008 Sep;6(3):219-24. doi: 10.1684/pnv.2008.0143. Psychol Neuropsychiatr Vieil. 2008. PMID: 18786881 Free article. Review. French.

9

Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain.

Brandel JP, Heath CA, Head MW, Levavasseur E, Knight R, Laplanche JL, Langeveld JP, Ironside JW, Hauw JJ, Mackenzie J, Alpérovitch A, Will RG, Haïk S. Brandel JP, et al. Ann Neurol. 2009 Mar;65(3):249-56. doi: 10.1002/ana.21583. Ann Neurol. 2009. PMID: 19334063

10

Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob disease.

Faucheux BA, Privat N, Brandel JP, Sazdovitch V, Laplanche JL, Maurage CA, Hauw JJ, Haïk S. Faucheux BA, et al. Among authors: brandel jp. J Neuropathol Exp Neurol. 2009 Aug;68(8):892-901. doi: 10.1097/NEN.0b013e3181af7f23. J Neuropathol Exp Neurol. 2009. PMID: 19606064

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