Hauw JJ - Search Results

1

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.

2

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

3

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

4

Dementia, the fate of brain? Neuropathological point of view.

Hauw JJ, Duyckaerts C. Hauw JJ, et al. C R Biol. 2002 Jun;325(6):655-64. doi: 10.1016/s1631-0691(02)01479-8. C R Biol. 2002. PMID: 12365416 Free article. Review.

5

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

6

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

7

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

8

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.

9

[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. Among authors: hauw jj. 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.

10

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.

Peoc'h K, Levavasseur E, Delmont E, De Simone A, Laffont-Proust I, Privat N, Chebaro Y, Chapuis C, Bedoucha P, Brandel JP, Laquerriere A, Kemeny JL, Hauw JJ, Borg M, Rezaei H, Derreumaux P, Laplanche JL, Haïk S. Peoc'h K, et al. Among authors: hauw jj. Hum Mol Genet. 2012 Dec 15;21(26):5417-28. doi: 10.1093/hmg/dds377. Epub 2012 Sep 10. Hum Mol Genet. 2012. PMID: 22965875

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