-
1
-
-
0034916581
-
Prion diseases of humans and animals: Their causes and molecular basis
-
Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 2001;24:519-50.
-
(2001)
Annu Rev Neurosci
, vol.24
, pp. 519-550
-
-
Collinge, J.1
-
2
-
-
21344445937
-
Molecular neurology of prion disease
-
Collinge J. Molecular neurology of prion disease. J Neurol Neurosurg Psychiatry 2005;76:906-19.
-
(2005)
J Neurol Neurosurg Psychiatry
, vol.76
, pp. 906-919
-
-
Collinge, J.1
-
3
-
-
0037385558
-
Phenotypic variability in the brains of a family with a prion disease chracterized by a 144-base pair insertion in the prion protein gene
-
King A, Doey L, Rossor M, et al. Phenotypic variability in the brains of a family with a prion disease chracterized by a 144-base pair insertion in the prion protein gene. Neuropathol Appl Neurobiol 2003;29:98-105.
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 98-105
-
-
King, A.1
Doey, L.2
Rossor, M.3
-
4
-
-
15444352327
-
Prion encephalopathy with insertion of octapeptide repeats: The number of repeats determines the type of cerebellar deposits
-
Vital C, Gray F, Vital A, et al. Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. Neuropathol Appl Neurobiol 1998;24:125-30.
-
(1998)
Neuropathol Appl Neurobiol
, vol.24
, pp. 125-130
-
-
Vital, C.1
Gray, F.2
Vital, A.3
-
5
-
-
0035943060
-
Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia
-
Beck JA, Mead S, Campbell TA, et al. Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia. Neurology 2001;57:354-6.
-
(2001)
Neurology
, vol.57
, pp. 354-356
-
-
Beck, J.A.1
Mead, S.2
Campbell, T.A.3
-
6
-
-
0026636605
-
Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies
-
Poulter M, Baker FM, Frith CD, et al. Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies. Brain 1992;115:675-85.
-
(1992)
Brain
, vol.115
, pp. 675-685
-
-
Poulter, M.1
Baker, F.M.2
Frith, C.D.3
-
7
-
-
0026650443
-
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
-
Collinge J, Brown J, Hardy J, et al. Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. Brain 1992;115:687-710.
-
(1992)
Brain
, vol.115
, pp. 687-710
-
-
Collinge, J.1
Brown, J.2
Hardy, J.3
-
8
-
-
0028946529
-
Inherited Creutzfeldt-Jakob disease in a British family associated with novel 144 base pair insertion of the prion protein gene
-
Nicholl D, Windl O, de Silva R, et al. Inherited Creutzfeldt-Jakob disease in a British family associated with novel 144 base pair insertion of the prion protein gene. J Neurol Neurosurg Psychiatry 1995;58:65-9.
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 65-69
-
-
Nicholl, D.1
Windl, O.2
de Silva, R.3
-
9
-
-
0029004216
-
Prion disease with 144 base pair insertion in a Japanese family line
-
Oda T, Kitamoto T, Tateishi J, et al. Prion disease with 144 base pair insertion in a Japanese family line. Acta Neuropathol 1995;90:80-6.
-
(1995)
Acta Neuropathol
, vol.90
, pp. 80-86
-
-
Oda, T.1
Kitamoto, T.2
Tateishi, J.3
-
10
-
-
0030756021
-
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family
-
Capellari S, Vital C, Parchi P, et al. Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. Neurology 1997;49:133-41.
-
(1997)
Neurology
, vol.49
, pp. 133-141
-
-
Capellari, S.1
Vital, C.2
Parchi, P.3
-
11
-
-
0037456356
-
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease
-
Zanusso G, Ferrari S, Cardone F, et al. Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease. N Engl J Med 2003;348:711-19.
-
(2003)
N Engl J Med
, vol.348
, pp. 711-719
-
-
Zanusso, G.1
Ferrari, S.2
Cardone, F.3
|