Brandel JP - Search Results

1

Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial.

Haïk S, Marcon G, Mallet A, Tettamanti M, Welaratne A, Giaccone G, Azimi S, Pietrini V, Fabreguettes JR, Imperiale D, Cesaro P, Buffa C, Aucan C, Lucca U, Peckeu L, Suardi S, Tranchant C, Zerr I, Houillier C, Redaelli V, Vespignani H, Campanella A, Sellal F, Krasnianski A, Seilhean D, Heinemann U, Sedel F, Canovi M, Gobbi M, Di Fede G, Laplanche JL, Pocchiari M, Salmona M, Forloni G, Brandel JP, Tagliavini F. Haïk S, et al. Among authors: brandel jp. Lancet Neurol. 2014 Feb;13(2):150-8. doi: 10.1016/S1474-4422(13)70307-7. Epub 2014 Jan 8. Lancet Neurol. 2014. PMID: 24411709 Clinical Trial.

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

Genetic prion disease: the EUROCJD experience.

Kovács GG, Puopolo M, Ladogana A, Pocchiari M, Budka H, van Duijn C, Collins SJ, Boyd A, Giulivi A, Coulthart M, Delasnerie-Laupretre N, Brandel JP, Zerr I, Kretzschmar HA, de Pedro-Cuesta J, Calero-Lara M, Glatzel M, Aguzzi A, Bishop M, Knight R, Belay G, Will R, Mitrova E; EUROCJD. Kovács GG, et al. Among authors: brandel jp. Hum Genet. 2005 Nov;118(2):166-74. doi: 10.1007/s00439-005-0020-1. Epub 2005 Nov 15. Hum Genet. 2005. PMID: 16187142

6

New ratios for the detection and classification of CJD in multisequence MRI of the brain.

Linguraru MG, Ayache N, González Ballester MA, Bardinet E, Galanaud D, Haïk S, Faucheux B, Cozzone P, Dormont D, Brandel JP. Linguraru MG, et al. Among authors: brandel jp. Med Image Comput Comput Assist Interv. 2005;8(Pt 2):492-9. doi: 10.1007/11566489_61. Med Image Comput Comput Assist Interv. 2005. PMID: 16685996

7

Iatrogenic Creutzfeldt-Jakob disease: the waning of an era.

Brown P, Brandel JP, Preece M, Sato T. Brown P, et al. Among authors: brandel jp. Neurology. 2006 Aug 8;67(3):389-93. doi: 10.1212/01.wnl.0000231528.65069.3f. Epub 2006 Jul 19. Neurology. 2006. PMID: 16855204

8

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

9

[Creutzfeldt-Jakob disease: what's new?].

Brandel JP. Brandel JP. Rev Prat. 2007 Oct 31;57(16):1745-7. Rev Prat. 2007. PMID: 18092714 French. No abstract available.

10

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

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