Hauw JJ - Search Results

1

Prion protein deposits match magnetic resonance imaging signal abnormalities in Creutzfeldt-Jakob disease.

Haïk S, Dormont D, Faucheux BA, Marsault C, Hauw JJ. Haïk S, et al. Among authors: hauw jj. Ann Neurol. 2002 Jun;51(6):797-9. doi: 10.1002/ana.10195. Ann Neurol. 2002. PMID: 12112094 No abstract available.

2

The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease.

Haïk S, Faucheux BA, Sazdovitch V, Privat N, Kemeny JL, Perret-Liaudet A, Hauw JJ. Haïk S, et al. Among authors: hauw jj. Nat Med. 2003 Sep;9(9):1121-3. doi: 10.1038/nm922. Epub 2003 Aug 24. Nat Med. 2003. PMID: 12937415

3

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: hauw jj. PLoS One. 2008 Jul 30;3(7):e2786. doi: 10.1371/journal.pone.0002786. PLoS One. 2008. PMID: 18665216 Free PMC article.

4

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. Among authors: hauw jj. Ann Neurol. 2009 Mar;65(3):249-56. doi: 10.1002/ana.21583. Ann Neurol. 2009. PMID: 19334063

5

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: hauw jj. J Neuropathol Exp Neurol. 2009 Aug;68(8):892-901. doi: 10.1097/NEN.0b013e3181af7f23. J Neuropathol Exp Neurol. 2009. PMID: 19606064

6

Different chromogranin immunoreactivity between prion and a-beta amyloid plaque.

Rangon CM, Haïk S, Faucheux BA, Metz-Boutigue MH, Fierville F, Fuchs JP, Hauw JJ, Aunis D. Rangon CM, et al. Among authors: hauw jj. Neuroreport. 2003 Apr 15;14(5):755-8. doi: 10.1097/00001756-200304150-00019. Neuroreport. 2003. PMID: 12692477

7

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: hauw jj. 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.

8

Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques.

Basset-Leobon C, Uro-Coste E, Peoc'h K, Haik S, Sazdovitch V, Rigal M, Andreoletti O, Hauw JJ, Delisle MB. Basset-Leobon C, et al. Among authors: hauw jj. Arch Neurol. 2006 Mar;63(3):449-52. doi: 10.1001/archneur.63.3.449. Arch Neurol. 2006. PMID: 16533975

9

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: hauw jj. Arch Neurol. 2008 Apr;65(4):545-9. doi: 10.1001/archneur.65.4.545. Arch Neurol. 2008. PMID: 18413481

10

Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14-3-3 protein, France, 1992 to 2009.

Peckeu L, Delasnerie-Lauprètre N, Brandel JP, Salomon D, Sazdovitch V, Laplanche JL, Duyckaerts C, Seilhean D, Haïk S, Hauw JJ. Peckeu L, et al. Among authors: hauw jj. Euro Surveill. 2017 Oct;22(41):16-00715. doi: 10.2807/1560-7917.ES.2017.22.41.16-00715. Euro Surveill. 2017. PMID: 29043964 Free PMC article.

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