-
1
-
-
0026481859
-
Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20
-
Brown P, Galvez S, Goldfarb LG, Nieto A, Cartier L, Gibbs CJ, Gajdusek DC (1992). Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20. J Neurol Sci 112:65-67.
-
(1992)
J Neurol Sci
, vol.112
, pp. 65-67
-
-
Brown, P.1
Galvez, S.2
Goldfarb, L.G.3
Nieto, A.4
Cartier, L.5
Gibbs, C.J.6
Gajdusek, D.C.7
-
2
-
-
0027404258
-
Inherited prion disease (PrP lysine 200) in Britain two cases reports
-
Collinge J, Palmer MS, Campbell T, Sidle KCL, Carroll D, Harding A (1993). Inherited prion disease (PrP lysine 200) in Britain two cases reports. Br Med J 306L:301-302.
-
(1993)
Br Med J
, vol.306 L
, pp. 301-302
-
-
Collinge, J.1
Palmer, M.S.2
Campbell, T.3
Sidle, K.C.L.4
Carroll, D.5
Harding, A.6
-
4
-
-
0018834536
-
Descriptive epidemiology of Creutzfeldt-Jakob in Chile
-
Galvez S, Masters C, Gajdusek DC (1980). Descriptive epidemiology of Creutzfeldt-Jakob in Chile. Arch Neurol 37:11-14.
-
(1980)
Arch Neurol
, vol.37
, pp. 11-14
-
-
Galvez, S.1
Masters, C.2
Gajdusek, D.C.3
-
5
-
-
0025280532
-
Identical mutation in unrelated patients with Creutzfeldt-Jakob disease
-
Goldfarb LG, Brown P, Goldgaber D, Garruto RM, Yanagihara R, Asher DM, Gajdusek DC (1990a). Identical mutation in unrelated patients with Creutzfeldt-Jakob disease. Lancet 336:174-175.
-
(1990)
Lancet
, vol.336
, pp. 174-175
-
-
Goldfarb, L.G.1
Brown, P.2
Goldgaber, D.3
Garruto, R.M.4
Yanagihara, R.5
Asher, D.M.6
Gajdusek, D.C.7
-
6
-
-
0024995430
-
Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
-
Goldfarb LG, Mitrova E, Brown P, Toh BH, Gajdusek DC (1990b). Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia. Lancet 336:514-515.
-
(1990)
Lancet
, vol.336
, pp. 514-515
-
-
Goldfarb, L.G.1
Mitrova, E.2
Brown, P.3
Toh, B.H.4
Gajdusek, D.C.5
-
7
-
-
0024992359
-
Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non Libyan origin
-
Goldfarb LG, Korczyn, AD, Brown P, Chapman J, Gajdusek DC (1990c). Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non Libyan origin. Lancet 336:637-638.
-
(1990)
Lancet
, vol.336
, pp. 637-638
-
-
Goldfarb, L.G.1
Korczyn, A.D.2
Brown, P.3
Chapman, J.4
Gajdusek, D.C.5
-
8
-
-
0025918142
-
Creutzfeldt-Jakob disease associated with the PRNP codon 200 mutation; an analysis of 45 families
-
Goldfarb LG, Brown P, Mitrova E, Cervenakova L, Goldin L, Korczyn AD, et al. (1991). Creutzfeldt-Jakob disease associated with the PRNP codon 200 mutation; an analysis of 45 families. Eur J Epidemiol 7:477-486.
-
(1991)
Eur J Epidemiol
, vol.7
, pp. 477-486
-
-
Goldfarb, L.G.1
Brown, P.2
Mitrova, E.3
Cervenakova, L.4
Goldin, L.5
Korczyn, A.D.6
-
9
-
-
0025869213
-
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
-
Hsiao K, Meiner Z, Kahana E, Cass C, Kahana I, Avrahami D, Scarlato G, et al (1991). Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. New Engl J Med 324:1091-1097.
-
(1991)
New Engl J Med
, vol.324
, pp. 1091-1097
-
-
Hsiao, K.1
Meiner, Z.2
Kahana, E.3
Cass, C.4
Kahana, I.5
Avrahami, D.6
Scarlato, G.7
-
10
-
-
0028206519
-
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
-
Inoue I, Kitamoto T, Doh-Ura K, Shii H, Goto I, Tateishi J (1994). Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene. Neurology 44:299-301.
-
(1994)
Neurology
, vol.44
, pp. 299-301
-
-
Inoue, I.1
Kitamoto, T.2
Doh-Ura, K.3
Shii, H.4
Goto, I.5
Tateishi, J.6
-
11
-
-
0016389681
-
Creutzfeldt-Jakob disease: Focus among Libyan Jews in Israel
-
Kahana E, Alter M, Braham J, Sofer D (1973). Creutzfeldt-Jakob disease: focus among Libyan Jews in Israel. Science 183:90-91.
-
(1973)
Science
, vol.183
, pp. 90-91
-
-
Kahana, E.1
Alter, M.2
Braham, J.3
Sofer, D.4
-
12
-
-
85046112812
-
Creutzfeldt-Jakob disease in a 52-year-old woman with florid plaques
-
Kopp N, Streichenberger N, Deslys JP, Laplanche JL, Chazot G (1996). Creutzfeldt-Jakob disease in a 52-year-old woman with florid plaques. Lancet 348:1240-1241.
-
(1996)
Lancet
, vol.348
, pp. 1240-1241
-
-
Kopp, N.1
Streichenberger, N.2
Deslys, J.P.3
Laplanche, J.L.4
Chazot, G.5
-
13
-
-
0028131841
-
Molecular genetics of prion diseases in France
-
Laplanche JL, Delasnerie-Laupretre N, Brandel JP, Chatelain J, Beaudry P, Alperovitch A, Launay JM (1994). Molecular genetics of prion diseases in France. Neurology 44:2347-2357.
-
(1994)
Neurology
, vol.44
, pp. 2347-2357
-
-
Laplanche, J.L.1
Delasnerie-Laupretre, N.2
Brandel, J.P.3
Chatelain, J.4
Beaudry, P.5
Alperovitch, A.6
Launay, J.M.7
-
14
-
-
0019778656
-
Creutzfeldt-Jakob disease virus isolation from Gerstmann-Sträussler syndrome with an analysis of the various form of amyloid plaque deposition in the virus-induced spongiform encephalopathies
-
Masters CL, Gajdusek DC, Gibbs CJ (1981). Creutzfeldt-Jakob disease virus isolation from Gerstmann-Sträussler syndrome with an analysis of the various form of amyloid plaque deposition in the virus-induced spongiform encephalopathies. Brain 104:559-588.
-
(1981)
Brain
, vol.104
, pp. 559-588
-
-
Masters, C.L.1
Gajdusek, D.C.2
Gibbs, C.J.3
-
15
-
-
0025990503
-
Some new aspects of CJD epidemiology in Slovakia
-
Mitrova E (1991). Some new aspects of CJD epidemiology in Slovakia. Eur J Epidemiol 7:439-449.
-
(1991)
Eur J Epidemiol
, vol.7
, pp. 439-449
-
-
Mitrova, E.1
-
16
-
-
0026015263
-
Focal accumulation of CJD in Slovakia: Retrospective investigation of a new rural familial cluster
-
Mitrova E, Brown P, Hroncova D, Tatara M, Zilak J (1991). Focal accumulation of CJD in Slovakia: retrospective investigation of a new rural familial cluster. Eur J Epidemioly 7:487-489.
-
(1991)
Eur J Epidemioly
, vol.7
, pp. 487-489
-
-
Mitrova, E.1
Brown, P.2
Hroncova, D.3
Tatara, M.4
Zilak, J.5
-
17
-
-
0030478022
-
Molecular biology and pathogenesis of prion diseases
-
Prusiner SB (1996). Molecular biology and pathogenesis of prion diseases. Trends Biochem Sci 21:482-487.
-
(1996)
Trends Biochem Sci
, vol.21
, pp. 482-487
-
-
Prusiner, S.B.1
-
18
-
-
0027425690
-
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease
-
Ripoll L, Laplanche JL, Salzmann M, Jouvet A, Planques B, Dussaucy M, et al. (1993). A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease. Neurology 43:1934-1938.
-
(1993)
Neurology
, vol.43
, pp. 1934-1938
-
-
Ripoll, L.1
Laplanche, J.L.2
Salzmann, M.3
Jouvet, A.4
Planques, B.5
Dussaucy, M.6
-
19
-
-
0030054675
-
Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease
-
Salvatore M, Pocchiari M, Cardone F, Petraroli R, D'Alessandro M, Galvez S, et al. (1996). Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiat 61:111-123.
-
(1996)
J Neurol Neurosurg Psychiat
, vol.61
, pp. 111-123
-
-
Salvatore, M.1
Pocchiari, M.2
Cardone, F.3
Petraroli, R.4
D'Alessandro, M.5
Galvez, S.6
|