Brown P - Search Results

1

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, et al. Goldfarb LG, et al. Among authors: brown p. Science. 1992 Oct 30;258(5083):806-8. doi: 10.1126/science.1439789. Science. 1992. PMID: 1439789

2

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. Ann Neurol. 1992 Mar;31(3):282-5. doi: 10.1002/ana.410310309. Ann Neurol. 1992. PMID: 1353342

3

The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease.

Brown P, Goldfarb LG, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. Eur J Epidemiol. 1991 Sep;7(5):469-76. doi: 10.1007/BF00143124. Eur J Epidemiol. 1991. PMID: 1684754

4

The transmissible spongiform encephalopathies.

Goldfarb LG, Brown P. Goldfarb LG, et al. Among authors: brown p. Annu Rev Med. 1995;46:57-65. doi: 10.1146/annurev.med.46.1.57. Annu Rev Med. 1995. PMID: 7598484 Review.

5

Molecular genetic studies of Creutzfeldt-Jakob disease.

Goldfarb LG, Brown P, Cervenakova L, Gajdusek DC. Goldfarb LG, et al. Among authors: brown p. Mol Neurobiol. 1994 Apr-Jun;8(2-3):89-97. doi: 10.1007/BF02780658. Mol Neurobiol. 1994. PMID: 7999318 Review.

6

Genetic analysis of Creutzfeldt-Jakob disease and related disorders.

Goldfarb LG, Brown P, Cervenakova L, Gajdusek DC. Goldfarb LG, et al. Among authors: brown p. Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):379-84. doi: 10.1098/rstb.1994.0032. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 8041803 Review.

7

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils.

Goldfarb LG, Brown P, Haltia M, Ghiso J, Frangione B, Gajdusek DC. Goldfarb LG, et al. Among authors: brown p. Proc Natl Acad Sci U S A. 1993 May 15;90(10):4451-4. doi: 10.1073/pnas.90.10.4451. Proc Natl Acad Sci U S A. 1993. PMID: 8506284 Free PMC article.

8

Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.

Cervenáková L, Goldfarb LG, Garruto R, Lee HS, Gajdusek DC, Brown P. Cervenáková L, et al. Among authors: brown p. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13239-41. doi: 10.1073/pnas.95.22.13239. Proc Natl Acad Sci U S A. 1998. PMID: 9789072 Free PMC article.

9

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG. Dagvadorj A, et al. Among authors: brown p. Ann Neurol. 2002 Sep;52(3):355-9. doi: 10.1002/ana.10267. Ann Neurol. 2002. PMID: 12205650

10

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: brown p. Ann Neurol. 1992 Mar;31(3):274-81. doi: 10.1002/ana.410310308. Ann Neurol. 1992. PMID: 1353341

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