-
1
-
-
0022447484
-
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
-
Lugaresi E, Medori R, Montagna P, et al. Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei. N Engl J Med 1986;315:997-1003.
-
(1986)
N Engl J Med
, vol.315
, pp. 997-1003
-
-
Lugaresi, E.1
Medori, R.2
Montagna, P.3
-
2
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
-
Medori R, Tritschler HJ, LeBlanc A, et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med 1992;326:444-449.
-
(1992)
N Engl J Med
, vol.326
, pp. 444-449
-
-
Medori, R.1
Tritschler, H.J.2
LeBlanc, A.3
-
3
-
-
0026496257
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism
-
Goldfarb LG, Petersen RB, Tabaton M, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science 1992; 258:806-808.
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
Petersen, R.B.2
Tabaton, M.3
-
4
-
-
0026690906
-
Fatal familial insomnia: A second kindred with mutation of prion gene at codon 178
-
Medori R, Montagna P, Tritschler HJ, et al. Fatal familial insomnia: a second kindred with mutation of prion gene at codon 178. Neurology 1992;42:669-670.
-
(1992)
Neurology
, vol.42
, pp. 669-670
-
-
Medori, R.1
Montagna, P.2
Tritschler, H.J.3
-
5
-
-
0026785544
-
Analysis of the prion gene in thalamic dementia
-
Petersen RB, Tabaton M, Berg L, et al. Analysis of the prion gene in thalamic dementia. Neurology 1992;42:1859-1863.
-
(1992)
Neurology
, vol.42
, pp. 1859-1863
-
-
Petersen, R.B.1
Tabaton, M.2
Berg, L.3
-
6
-
-
0027763639
-
Fatal familial insomnia and the widening spectrum of prion diseases
-
Gambetti P, Petersen R, Monari L, et al. Fatal familial insomnia and the widening spectrum of prion diseases. Br Med Bull 1993;49:980-994.
-
(1993)
Br Med Bull
, vol.49
, pp. 980-994
-
-
Gambetti, P.1
Petersen, R.2
Monari, L.3
-
7
-
-
0026801958
-
A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease
-
Bosque PJ, Vnencak-Jones C, Johnson MD, Whitlock JA, McLean MJ. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease. Neurology 1992;42:1864-1870.
-
(1992)
Neurology
, vol.42
, pp. 1864-1870
-
-
Bosque, P.J.1
Vnencak-Jones, C.2
Johnson, M.D.3
Whitlock, J.A.4
McLean, M.J.5
-
8
-
-
0029031422
-
Clinical and genetic studies of fatal familial insomnia
-
Reder AT, Mednick AS, Brown P, et al. Clinical and genetic studies of fatal familial insomnia. Neurology 1995;45:1068-1075.
-
(1995)
Neurology
, vol.45
, pp. 1068-1075
-
-
Reder, A.T.1
Mednick, A.S.2
Brown, P.3
-
9
-
-
0029961971
-
Fatal familial insomnia with a mutation at codon 178 of the prion protein gene
-
Nagayama M, Shinohara Y, Furukawa H, Kitamoto T. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene. Neurology 1996;47:1313-1316.
-
(1996)
Neurology
, vol.47
, pp. 1313-1316
-
-
Nagayama, M.1
Shinohara, Y.2
Furukawa, H.3
Kitamoto, T.4
-
10
-
-
0029143542
-
Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy
-
Brown P, Kenney K, Little B, et al. Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy. Ann Neurol 1995;38:245-253.
-
(1995)
Ann Neurol
, vol.38
, pp. 245-253
-
-
Brown, P.1
Kenney, K.2
Little, B.3
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