Laplanche JL - Search Results

1

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

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

2

[Molecular genetics of familial and sporadic forms of human prion diseases].

Laplanche JL, Launay JM, Dreux C. Laplanche JL, et al. Ann Pharm Fr. 1995;53(5):193-200. Ann Pharm Fr. 1995. PMID: 7503507 Review. French.

3

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. Neurology. 1994 Dec;44(12):2347-51. doi: 10.1212/wnl.44.12.2347. Neurology. 1994. PMID: 7991124

4

PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis.

Laplanche JL, Chatelain J, Westaway D, Thomas S, Dussaucy M, Brugere-Picoux J, Launay JM. Laplanche JL, et al. Genomics. 1993 Jan;15(1):30-7. doi: 10.1006/geno.1993.1006. Genomics. 1993. PMID: 8094373

5

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: laplanche jl. Neurology. 1993 Oct;43(10):1934-8. doi: 10.1212/wnl.43.10.1934. Neurology. 1993. PMID: 8105421

6

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases.

Peoc'h K, Guérin C, Brandel JP, Launay JM, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Neurosci Lett. 2000 Jun 2;286(2):144-8. doi: 10.1016/s0304-3940(00)01100-9. Neurosci Lett. 2000. PMID: 10825657

7

A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease.

Rodriguez MM, Peoc'h K, Haïk S, Bouchet C, Vernengo L, Mañana G, Salamano R, Carrasco L, Lenne M, Beaudry P, Launay JM, Laplanche JL. Rodriguez MM, et al. Among authors: laplanche jl. Neurology. 2005 Apr 26;64(8):1455-7. doi: 10.1212/01.WNL.0000158618.39527.93. Neurology. 2005. PMID: 15851745

8

Deletion in prion protein gene in a Moroccan family.

Laplanche JL, Chatelain J, Launay JM, Gazengel C, Vidaud M. Laplanche JL, et al. Nucleic Acids Res. 1990 Nov 25;18(22):6745. doi: 10.1093/nar/18.22.6745. Nucleic Acids Res. 1990. PMID: 1979164 Free PMC article.

9

Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie.

Clouscard C, Beaudry P, Elsen JM, Milan D, Dussaucy M, Bounneau C, Schelcher F, Chatelain J, Launay JM, Laplanche JL. Clouscard C, et al. Among authors: laplanche jl. J Gen Virol. 1995 Aug;76 ( Pt 8):2097-101. doi: 10.1099/0022-1317-76-8-2097. J Gen Virol. 1995. PMID: 7636494

10

Two novel insertions in the prion protein gene in patients with late-onset dementia.

Laplanche JL, Delasnerie-Lauprêtre N, Brandel JP, Dussaucy M, Chatelain J, Launay JM. Laplanche JL, et al. Hum Mol Genet. 1995 Jun;4(6):1109-11. doi: 10.1093/hmg/4.6.1109. Hum Mol Genet. 1995. PMID: 7655470 No abstract available.

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