Goldfarb LG - Search Results

1

Kuru: genes, cannibals and neuropathology.

Liberski PP, Sikorska B, Lindenbaum S, Goldfarb LG, McLean C, Hainfellner JA, Brown P. Liberski PP, et al. Among authors: goldfarb lg. J Neuropathol Exp Neurol. 2012 Feb;71(2):92-103. doi: 10.1097/NEN.0b013e3182444efd. J Neuropathol Exp Neurol. 2012. PMID: 22249461 Free PMC article. Review.

2

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: goldfarb lg. Neurology. 2000 Jun 13;54(11):2133-7. doi: 10.1212/wnl.54.11.2133. Neurology. 2000. PMID: 10851377

3

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. Exp Neurol. 1990 Jun;108(3):247-50. doi: 10.1016/0014-4886(90)90130-k. Exp Neurol. 1990. PMID: 2190844

4

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: goldfarb lg. Neurology. 1998 Aug;51(2):548-53. doi: 10.1212/wnl.51.2.548. Neurology. 1998. PMID: 9710033

5

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: goldfarb lg. Eur J Epidemiol. 1991 Sep;7(5):494-500. doi: 10.1007/BF00143128. Eur J Epidemiol. 1991. PMID: 1684756

6

The transmissible spongiform encephalopathies.

Goldfarb LG, Brown P. Goldfarb LG, et al. Annu Rev Med. 1995;46:57-65. doi: 10.1146/annurev.med.46.1.57. Annu Rev Med. 1995. PMID: 7598484 Review.

7

Creutzfeldt-Jakob disease in a husband and wife.

Brown P, Cervenáková L, McShane L, Goldfarb LG, Bishop K, Bastian F, Kirkpatrick J, Piccardo P, Ghetti B, Gajdusek DC. Brown P, et al. Among authors: goldfarb lg. Neurology. 1998 Mar;50(3):684-8. doi: 10.1212/wnl.50.3.684. Neurology. 1998. PMID: 9521256

8

Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation.

Cochran EJ, Bennett DA, Cervenáková L, Kenney K, Bernard B, Foster NL, Benson DF, Goldfarb LG, Brown P. Cochran EJ, et al. Among authors: goldfarb lg. Neurology. 1996 Sep;47(3):727-33. doi: 10.1212/wnl.47.3.727. Neurology. 1996. PMID: 8797471

9

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. Among authors: goldfarb lg. Ann Neurol. 1994 May;35(5):513-29. doi: 10.1002/ana.410350504. Ann Neurol. 1994. PMID: 8179297

10

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

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