Brown P - Search Results

1

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.

2

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.

3

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

4

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

5

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: brown p. J Neurol Sci. 1992 Sep;111(2):189-94. doi: 10.1016/0022-510x(92)90067-u. J Neurol Sci. 1992. PMID: 1431985

6

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

7

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

8

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.

Goldfarb LG, Brown P, Mitrovà E, Cervenáková L, Goldin L, Korczyn AD, Chapman J, Gálvez S, Cartier L, Rubenstein R, et al. Goldfarb LG, et al. Among authors: brown p. Eur J Epidemiol. 1991 Sep;7(5):477-86. doi: 10.1007/BF00143125. Eur J Epidemiol. 1991. PMID: 1684755

9

A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin.

Korczyn AD, Chapman J, Goldfarb LG, Brown P, Gajdusek DC. Korczyn AD, et al. Among authors: brown p. Ann N Y Acad Sci. 1991;640:171-6. doi: 10.1111/j.1749-6632.1991.tb00211.x. Ann N Y Acad Sci. 1991. PMID: 1685643

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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