Brown P - Search Results

1

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

2

Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.

Chapman J, Brown P, Rabey JM, Goldfarb LG, Inzelberg R, Gibbs CJ Jr, Gajdusek DC, Korczyn AD. Chapman J, et al. Among authors: brown p. Neurology. 1992 Jun;42(6):1249-50. doi: 10.1212/wnl.42.6.1249-a. Neurology. 1992. PMID: 1351274 No abstract available.

3

Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy.

Bertoni JM, Brown P, Goldfarb LG, Rubenstein R, Gajdusek DC. Bertoni JM, et al. Among authors: brown p. JAMA. 1992 Nov 4;268(17):2413-5. JAMA. 1992. PMID: 1404799

4

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.

5

Alzheimer's disease and transmissible virus dementia (Creutzfeldt-Jakob disease).

Brown P, Salazar AM, Gibbs CJ Jr, Gajdusek DC. Brown P, et al. Ann N Y Acad Sci. 1982;396:131-43. doi: 10.1111/j.1749-6632.1982.tb26849.x. Ann N Y Acad Sci. 1982. PMID: 6758661

6

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

Chapman J, Brown P, Goldfarb LG, Arlazoroff A, Gajdusek DC, Korczyn AD. Chapman J, et al. Among authors: brown p. J Neurol Neurosurg Psychiatry. 1993 Oct;56(10):1109-12. doi: 10.1136/jnnp.56.10.1109. J Neurol Neurosurg Psychiatry. 1993. PMID: 8105028 Free PMC article.

7

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD. Chapman J, et al. Among authors: brown p. Neurology. 1996 Mar;46(3):758-61. doi: 10.1212/wnl.46.3.758. Neurology. 1996. PMID: 8618678

8

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.

9

Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968--1977.

Brown P, Cathala F, Sadowsky D, Gajdusek DC. Brown P, et al. Ann Neurol. 1979 Nov;6(5):430-7. doi: 10.1002/ana.410060510. Ann Neurol. 1979. PMID: 391141

10

Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968--1977.

Brown P, Cathala F, Gajdusek DC. Brown P, et al. Ann Neurol. 1979 Nov;6(5):438-46. doi: 10.1002/ana.410060511. Ann Neurol. 1979. PMID: 391142

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