Gajdusek DC - Search Results

1

Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus.

Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G. Lunkes A, et al. Among authors: gajdusek dc. Exp Neurol. 1994 Apr;126(2):310-2. doi: 10.1006/exnr.1994.1070. Exp Neurol. 1994. PMID: 7925830

2

Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.

Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC. Goldfarb LG, et al. Among authors: gajdusek dc. Ann Neurol. 1996 Apr;39(4):500-6. doi: 10.1002/ana.410390412. Ann Neurol. 1996. PMID: 8619528

3

Olivopontocerebellar atrophy in a large Iakut kinship in eastern Siberia.

Goldfarb LG, Chumakov MP, Petrov PA, Fedorova NI, Gajdusek DC. Goldfarb LG, et al. Among authors: gajdusek dc. Neurology. 1989 Nov;39(11):1527-30. doi: 10.1212/wnl.39.11.1527. Neurology. 1989. PMID: 2812335

4

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: gajdusek dc. Neurology. 1992 Jun;42(6):1249-50. doi: 10.1212/wnl.42.6.1249-a. Neurology. 1992. PMID: 1351274 No abstract available.

5

Viliuisk encephalomyelitis in the Iakut people of Siberia.

Goldfarb LG, Gajdusek DC. Goldfarb LG, et al. Among authors: gajdusek dc. Brain. 1992 Aug;115 ( Pt 4):961-78. doi: 10.1093/brain/115.4.961. Brain. 1992. PMID: 1393513

6

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: gajdusek dc. Neurology. 1996 Mar;46(3):758-61. doi: 10.1212/wnl.46.3.758. Neurology. 1996. PMID: 8618678

7

APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies.

Chapman J, Cervenáková L, Petersen RB, Lee HS, Estupinan J, Richardson S, Vnencak-Jones CL, Gajdusek DC, Korczyn AD, Brown P, Goldfarb LG. Chapman J, et al. Among authors: gajdusek dc. Neurology. 1998 Aug;51(2):548-53. doi: 10.1212/wnl.51.2.548. Neurology. 1998. PMID: 9710033

8

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: gajdusek dc. JAMA. 1992 Nov 4;268(17):2413-5. JAMA. 1992. PMID: 1404799

9

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: gajdusek dc. 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.

10

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: gajdusek dc. Neurology. 1991 Mar;41(3):375-9. doi: 10.1212/wnl.41.3.375. Neurology. 1991. PMID: 1672447

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