Beaudry P - Search Results

1

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

Laplanche JL, Delasnerie-Lauprêtre N, Brandel JP, Chatelain J, Beaudry P, Alpérovitch A, Launay JM. Laplanche JL, et al. Among authors: beaudry p. Neurology. 1994 Dec;44(12):2347-51. doi: 10.1212/wnl.44.12.2347. Neurology. 1994. PMID: 7991124

2

[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies].

Laplanche JL, Beaudry P, Ripoll L, Launay JM. Laplanche JL, et al. Among authors: beaudry p. Pathol Biol (Paris). 1995 Feb;43(2):104-13. Pathol Biol (Paris). 1995. PMID: 7777379 Review. French.

3

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.

Ripoll L, Laplanche JL, Salzmann M, Jouvet A, Planques B, Dussaucy M, Chatelain J, Beaudry P, Launay JM. Ripoll L, et al. Among authors: beaudry p. Neurology. 1993 Oct;43(10):1934-8. doi: 10.1212/wnl.43.10.1934. Neurology. 1993. PMID: 8105421

4

Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene.

Antoine JC, Laplanche JL, Mosnier JF, Beaudry P, Chatelain J, Michel D. Antoine JC, et al. Among authors: beaudry p. Neurology. 1996 Apr;46(4):1123-7. doi: 10.1212/wnl.46.4.1123. Neurology. 1996. PMID: 8780103

5

Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma.

Antoine JC, Michel D, Bertholon P, Mosnier JF, Laplanche JL, Beaudry P, Hauw JJ, Veyret C. Antoine JC, et al. Among authors: beaudry p. Neurology. 1997 May;48(5):1451-3. doi: 10.1212/wnl.48.5.1451. Neurology. 1997. PMID: 9153491

6

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.

Peoc'h K, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-Lauprêtre N, Laplanche JL. Peoc'h K, et al. Among authors: beaudry p. Hum Mutat. 2000 May;15(5):482. doi: 10.1002/(SICI)1098-1004(200005)15:5<482::AID-HUMU16>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10790216

7

14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients.

Brandel JP, Peoc'h K, Beaudry P, Welaratne A, Bottos C, Agid Y, Laplanche JL. Brandel JP, et al. Among authors: beaudry p. Ann Neurol. 2001 Feb;49(2):257-60. doi: 10.1002/1531-8249(20010201)49:2<257::aid-ana48>3.0.co;2-x. Ann Neurol. 2001. PMID: 11220747

8

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.

Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary JY, Laplanche JL. Beaudry P, et al. Eur J Neurol. 2002 Sep;9(5):457-62. doi: 10.1046/j.1468-1331.2002.00456.x. Eur J Neurol. 2002. PMID: 12220376

9

Creutzfeldt-Jakob disease and cerebral amyloid angiopathy.

Gray F, Chrétien F, Cesaro P, Chatelain J, Beaudry P, Laplanche JL, Mikol J, Bell J, Gambetti P, Degos JD. Gray F, et al. Among authors: beaudry p. Acta Neuropathol. 1994;88(1):106-11. doi: 10.1007/BF00294366. Acta Neuropathol. 1994. PMID: 7941967

10

French autochthonous scrapied sheep without the 136Val PrP polymorphism.

Laplanche JL, Chatelain J, Beaudry P, Dussaucy M, Bounneau C, Launay JM. Laplanche JL, et al. Among authors: beaudry p. Mamm Genome. 1993;4(8):463-4. doi: 10.1007/BF00296824. Mamm Genome. 1993. PMID: 8104061 No abstract available.

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