Brown P - Search Results

1

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.

2

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

3

Comparison of cell-fusing activity of brain suspensions from patients with Creutzfeldt-Jakob disease and other degenerative neurological diseases.

Moreau-Dubois MC, Brown P, Gajdusek DC. Moreau-Dubois MC, et al. Among authors: brown p. Proc Natl Acad Sci U S A. 1979 Oct;76(10):5365-7. doi: 10.1073/pnas.76.10.5365. Proc Natl Acad Sci U S A. 1979. PMID: 388435 Free PMC article.

4

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

5

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

6

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

7

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

Brown P, Gálvez S, Goldfarb LG, Nieto A, Cartier L, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. J Neurol Sci. 1992 Oct;112(1-2):65-7. doi: 10.1016/0022-510x(92)90133-6. J Neurol Sci. 1992. PMID: 1469441

8

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, Cervenakova L, Baron H, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: brown p. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10926-30. doi: 10.1073/pnas.88.23.10926. Proc Natl Acad Sci U S A. 1991. PMID: 1683708 Free PMC article.

9

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

10

The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.

Brown P, Gajdusek DC. Brown P, et al. Curr Top Microbiol Immunol. 1991;172:1-20. doi: 10.1007/978-3-642-76540-7_1. Curr Top Microbiol Immunol. 1991. PMID: 1687378 Review. No abstract available.

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