Brown P - Search Results

1

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome.

Brown P, Goldfarb LG, Brown WT, Goldgaber D, Rubenstein R, Kascsak RJ, Guiroy DC, Piccardo P, Boellaard JW, Gajdusek DC. Brown P, et al. Among authors: brown wt. Neurology. 1991 Mar;41(3):375-9. doi: 10.1212/wnl.41.3.375. Neurology. 1991. PMID: 1672447

2

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

3

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

4

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

5

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.

6

A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease.

Brown P, Wolff A, Gajdusek DC. Brown P, et al. Neurology. 1990 Jun;40(6):887-90. doi: 10.1212/wnl.40.6.887. Neurology. 1990. PMID: 1693181

7

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene.

Brown P, Goldfarb LG, McCombie WR, Nieto A, Squillacote D, Sheremata W, Little BW, Godec MS, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. Neurology. 1992 Feb;42(2):422-7. doi: 10.1212/wnl.42.2.422. Neurology. 1992. PMID: 1736177

8

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome.

Goldfarb LG, Brown P, Goldgaber D, Asher DM, Rubenstein R, Brown WT, Piccardo P, Kascsak RJ, Boellaard JW, Gajdusek DC. Goldfarb LG, et al. Among authors: brown wt, brown p. Exp Neurol. 1990 Jun;108(3):247-50. doi: 10.1016/0014-4886(90)90130-k. Exp Neurol. 1990. PMID: 2190844

9

Coexistence of Creutzfeldt-Jakob disease and Alzheimer's disease in the same patient.

Brown P, Jannotta F, Gibbs CJ Jr, Baron H, Guiroy DC, Gajdusek DC. Brown P, et al. Neurology. 1990 Feb;40(2):226-8. doi: 10.1212/wnl.40.2.226. Neurology. 1990. PMID: 2405293

10

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.

Goldgaber D, Goldfarb LG, Brown P, Asher DM, Brown WT, Lin S, Teener JW, Feinstone SM, Rubenstein R, Kascsak RJ, et al. Goldgaber D, et al. Among authors: brown wt, brown p. Exp Neurol. 1989 Nov;106(2):204-6. doi: 10.1016/0014-4886(89)90095-2. Exp Neurol. 1989. PMID: 2572450

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