Cathala F - Search Results

1

Why I joined the research laboratory of Prof. D. Carleton Gajdusek in 1968.

Cathala F. Cathala F. Philos Trans R Soc Lond B Biol Sci. 2008 Nov 27;363(1510):3631-2. doi: 10.1098/rstb.2008.4008. Philos Trans R Soc Lond B Biol Sci. 2008. PMID: 18849253 Free PMC article. No abstract available.

2

[Brief history of transmissible spongiform encephalopathies].

Brown P, Bradley R, Cathala F. Brown P, et al. Among authors: cathala f. Rev Prat. 1999 May 1;49(9):928-33. Rev Prat. 1999. PMID: 11865456 French.

3

Natural and experimental oral infection of nonhuman primates by bovine spongiform encephalopathy agents.

Bons N, Mestre-Frances N, Belli P, Cathala F, Gajdusek DC, Brown P. Bons N, et al. Among authors: cathala f. Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):4046-51. doi: 10.1073/pnas.96.7.4046. Proc Natl Acad Sci U S A. 1999. PMID: 10097160 Free PMC article.

4

[Human spongiform encephalopathies].

Cathala F. Cathala F. Pathol Biol (Paris). 1995 Jan;43(1):6-21. Pathol Biol (Paris). 1995. PMID: 7777378 Review. French.

5

[A funny story].

Cathala F. Cathala F. Pathol Biol (Paris). 1995 Jan;43(1):3-5. Pathol Biol (Paris). 1995. PMID: 7777376 French. No abstract available.

6

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family.

Goldfarb LG, Brown P, Vrbovská A, Baron H, McCombie WR, Cathala F, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: cathala f. J Neurol Sci. 1992 Sep;111(2):189-94. doi: 10.1016/0022-510x(92)90067-u. J Neurol Sci. 1992. PMID: 1431985

7

Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation.

Brown P, Goldfarb LG, Kovanen J, Haltia M, Cathala F, Sulima M, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. Among authors: cathala f. Ann Neurol. 1992 Mar;31(3):282-5. doi: 10.1002/ana.410310309. Ann Neurol. 1992. PMID: 1353342

8

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin.

Goldfarb LG, Brown P, Haltia M, Cathala F, McCombie WR, Kovanen J, Cervenáková L, Goldin L, Nieto A, Godec MS, et al. Goldfarb LG, et al. Among authors: cathala f. Ann Neurol. 1992 Mar;31(3):274-81. doi: 10.1002/ana.410310308. Ann Neurol. 1992. PMID: 1353341

9

The molecular genetics of familial Creutzfeldt-Jakob disease in France.

Brown P, Goldfarb LG, Cathala F, Vrbovská A, Sulima M, Nieto A, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. Among authors: cathala f. J Neurol Sci. 1991 Oct;105(2):240-6. doi: 10.1016/0022-510x(91)90151-v. J Neurol Sci. 1991. PMID: 1757800

10

[Analysis of the PrP gene in a Tunisian family with Creutzfeldt-Jakob disease].

Laplanche JL, Chatelain J, Thomas S, Brown P, Cathala F. Laplanche JL, et al. Among authors: cathala f. Rev Neurol (Paris). 1991;147(12):825-7. Rev Neurol (Paris). 1991. PMID: 1780610 French.

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