Brown P - Search Results

1

Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description.

Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R, et al. Haltia M, et al. Among authors: brown p. Ann Neurol. 1994 Sep;36(3):362-7. doi: 10.1002/ana.410360307. Ann Neurol. 1994. PMID: 8080244

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

Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.

Haltia M, Kovanen J, Goldfarb LG, Brown P, Gajdusek DC. Haltia M, et al. Among authors: brown p. Eur J Epidemiol. 1991 Sep;7(5):494-500. doi: 10.1007/BF00143128. Eur J Epidemiol. 1991. PMID: 1684756

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

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.

6

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.

7

A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype.

Majtényi C, Brown P, Cervenáková L, Goldfarb LG, Tateishi J. Majtényi C, et al. Among authors: brown p. Neurology. 2000 Jun 13;54(11):2133-7. doi: 10.1212/wnl.54.11.2133. Neurology. 2000. PMID: 10851377

8

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

9

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

10

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

Brown P, Gibbs CJ Jr, Rodgers-Johnson P, Asher DM, Sulima MP, Bacote A, Goldfarb LG, Gajdusek DC. Brown P, et al. Ann Neurol. 1994 May;35(5):513-29. doi: 10.1002/ana.410350504. Ann Neurol. 1994. PMID: 8179297

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