-
1
-
-
9144221019
-
Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease
-
Steinhoff BJ, Zerr I, Glatting M, et al. Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease. Ann Neurol 2004;56:702-708.
-
(2004)
Ann Neurol
, vol.56
, pp. 702-708
-
-
Steinhoff, B.J.1
Zerr, I.2
Glatting, M.3
-
2
-
-
3543061151
-
Sporadic Creutzfeldt-Jakob disease: Magnetic resonance imaging and clinical findings
-
Meissner B, Köhler K, Körtner K, et al. Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings. Neurology 2004;63:450-456.
-
(2004)
Neurology
, vol.63
, pp. 450-456
-
-
Meissner, B.1
Köhler, K.2
Körtner, K.3
-
3
-
-
0033844156
-
Current clinical diagnosis in CJD: Identification of uncommon variants
-
Zerr I, Schulz-Schaeffer WJ, Giese A, et al. Current clinical diagnosis in CJD: identification of uncommon variants. Ann Neurol 2000;48:323-329.
-
(2000)
Ann Neurol
, vol.48
, pp. 323-329
-
-
Zerr, I.1
Schulz-Schaeffer, W.J.2
Giese, A.3
-
4
-
-
0034234437
-
Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia
-
Parchi P, Capellari S, Gambetti P. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia. Microsc Res Tech 2000;50:16-25.
-
(2000)
Microsc Res Tech
, vol.50
, pp. 16-25
-
-
Parchi, P.1
Capellari, S.2
Gambetti, P.3
-
5
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
-
Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996;39:767-778.
-
(1996)
Ann Neurol
, vol.39
, pp. 767-778
-
-
Parchi, P.1
Castellani, R.2
Capellari, S.3
-
6
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
-
Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;46:224-233.
-
(1999)
Ann Neurol
, vol.46
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
-
7
-
-
15144348474
-
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995
-
EU Collaborative Study Group for CJD
-
Will RG, Alpérovitch A, Poser S, et al. Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD. Ann Neurol 1998;43:763-767.
-
(1998)
Ann Neurol
, vol.43
, pp. 763-767
-
-
Will, R.G.1
Alpérovitch, A.2
Poser, S.3
-
8
-
-
0033562770
-
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
-
Alpérovitch A, Zerr I, Pocchiari M, et al. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease. Lancet 1999;353:1673-1674.
-
(1999)
Lancet
, vol.353
, pp. 1673-1674
-
-
Alpérovitch, A.1
Zerr, I.2
Pocchiari, M.3
-
9
-
-
4944246589
-
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
-
Pocchiari M, Poupolo M, Croes EA, et al. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain 2004;10:2348-2359.
-
(2004)
Brain
, vol.10
, pp. 2348-2359
-
-
Pocchiari, M.1
Poupolo, M.2
Croes, E.A.3
-
10
-
-
0342951746
-
A new variant of Creuczfeldt-Jakob disease in the UK
-
Will RG, Ironside JW, Zeidler M, et al. A new variant of Creuczfeldt-Jakob disease in the UK. Lancet 1996;347:921-925.
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
-
11
-
-
0031588170
-
New variant Creutzfeldt-Jakob disease: Psychiatric features
-
Zeidler M, Johnstone EC, Bamber RW, et al. New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet 1997;350:908-910.
-
(1997)
Lancet
, vol.350
, pp. 908-910
-
-
Zeidler, M.1
Johnstone, E.C.2
Bamber, R.W.3
-
12
-
-
0037157534
-
First hundred cases of variant Creutzfeldt-Jakob disease: Retrospective case note review of early psychiatric and neurological features
-
Spencer MD, Knight RS, Will RG. First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features. BMJ 2002;324:1479-1482.
-
(2002)
BMJ
, vol.324
, pp. 1479-1482
-
-
Spencer, M.D.1
Knight, R.S.2
Will, R.G.3
-
13
-
-
0034718472
-
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease
-
Zerr I, Pocchiari M, Collins S, et al. Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology 2000;55:811-815.
-
(2000)
Neurology
, vol.55
, pp. 811-815
-
-
Zerr, I.1
Pocchiari, M.2
Collins, S.3
-
14
-
-
0032553667
-
Human transmissible spongiform encephalopathies
-
WHO. Human transmissible spongiform encephalopathies. Wkly Epidemiol Rec 1998;47:361-365.
-
(1998)
Wkly Epidemiol Rec
, vol.47
, pp. 361-365
-
-
-
15
-
-
0032747378
-
How to improve the clinical diagnosis of Creutzfeldt-Jakob disease
-
Poser S, Mollenhauer B, Krauss A, et al. How to improve the clinical diagnosis of Creutzfeldt-Jakob disease. Brain 1999;122:2345-2351.
-
(1999)
Brain
, vol.122
, pp. 2345-2351
-
-
Poser, S.1
Mollenhauer, B.2
Krauss, A.3
-
16
-
-
0033874288
-
The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases
-
Schulz-Schaeffer WJ, Tschoke S, Kranefuss N, et al. The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases. Am J Pathol 2000;156:51-56.
-
(2000)
Am J Pathol
, vol.156
, pp. 51-56
-
-
Schulz-Schaeffer, W.J.1
Tschoke, S.2
Kranefuss, N.3
-
17
-
-
0032843132
-
Molecular generics of human prion diseases in Germany
-
Windl O, Giese A, Schulz-Schaeffer W, et al. Molecular generics of human prion diseases in Germany. Hum Genet 1999;105:244-252.
-
(1999)
Hum Genet
, vol.105
, pp. 244-252
-
-
Windl, O.1
Giese, A.2
Schulz-Schaeffer, W.3
-
18
-
-
0025372832
-
A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease
-
Brown P, Wolff A, Gajdusek DC. A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease. Neurology 1990;40:887-890.
-
(1990)
Neurology
, vol.40
, pp. 887-890
-
-
Brown, P.1
Wolff, A.2
Gajdusek, D.C.3
-
19
-
-
0026751775
-
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
-
Kitamoto T, Shin RW, Doh-Ura K, et al. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 1992;140:1285-1294.
-
(1992)
Am J Pathol
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.W.2
Doh-Ura, K.3
-
21
-
-
0030056269
-
Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease
-
Steinhoff BJ, Racker S, Herrendorf G, et al. Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol 1996;53:162-166.
-
(1996)
Arch Neurol
, vol.53
, pp. 162-166
-
-
Steinhoff, B.J.1
Racker, S.2
Herrendorf, G.3
-
22
-
-
0033671957
-
Magnetic resonance imaging (MRI) in the clinical diagnosis of Creutzfeldt-Jakob disease
-
Schroter A, Zerr I, Henkel K, et al. Magnetic resonance imaging (MRI) in the clinical diagnosis of Creutzfeldt-Jakob disease. Arch Neurol 2000;57:1751-1757.
-
(2000)
Arch Neurol
, vol.57
, pp. 1751-1757
-
-
Schroter, A.1
Zerr, I.2
Henkel, K.3
-
23
-
-
0031594134
-
MRI in sporadic Creutzfeldt-Jakob disease: Correlation with clinical and neuropathological data
-
Urbach H, Klisch J, Wolf HK, et al. MRI in sporadic Creutzfeldt-Jakob disease: correlation with clinical and neuropathological data. Neuroradiology 1998;40:65-70.
-
(1998)
Neuroradiology
, vol.40
, pp. 65-70
-
-
Urbach, H.1
Klisch, J.2
Wolf, H.K.3
-
24
-
-
3543144260
-
Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease
-
Shiga Y, Miyazawa K, Sato S, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Neurology 2004;63:443-449.
-
(2004)
Neurology
, vol.63
, pp. 443-449
-
-
Shiga, Y.1
Miyazawa, K.2
Sato, S.3
-
25
-
-
0031914675
-
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
-
Zerr I, Bodemer M, Gefeller O, et al. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol 1998;43:32-40.
-
(1998)
Ann Neurol
, vol.43
, pp. 32-40
-
-
Zerr, I.1
Bodemer, M.2
Gefeller, O.3
-
26
-
-
0032249499
-
Atypical case of sporadic Creutzfeldt-Jakob disease (CJD) in a young adult
-
Kozubski W, Wender M, Szczech J, et al. Atypical case of sporadic Creutzfeldt-Jakob disease (CJD) in a young adult. Folia Neuropathol 1998;36:225-228.
-
(1998)
Folia Neuropathol
, vol.36
, pp. 225-228
-
-
Kozubski, W.1
Wender, M.2
Szczech, J.3
-
28
-
-
0023243707
-
The epidemiology of Creutzfeldt-Jakob disease: Conclusion of a 15-year investigation in France and review of the world literature
-
Brown P, Cathala F, Raubertas RF, et al. The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature. Neurology 1987;37:895-904.
-
(1987)
Neurology
, vol.37
, pp. 895-904
-
-
Brown, P.1
Cathala, F.2
Raubertas, R.F.3
-
29
-
-
0028235176
-
Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
-
Brown P, Gibbs CJ Jr, Rodgers-Johnson P, et al. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 1994;35:513-529.
-
(1994)
Ann Neurol
, vol.35
, pp. 513-529
-
-
Brown, P.1
Gibbs Jr., C.J.2
Rodgers-Johnson, P.3
-
30
-
-
20944445878
-
Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Austria and Canada
-
Ladogana A, Puopolo M, Croes EA, et al. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Austria and Canada. Neurology 2004;64:1586-1591.
-
(2004)
Neurology
, vol.64
, pp. 1586-1591
-
-
Ladogana, A.1
Puopolo, M.2
Croes, E.A.3
-
31
-
-
0027288618
-
Clinical characteristics of familial and sporadic Creutzfeldt-Jakob disease in Finland
-
Kovanen J. Clinical characteristics of familial and sporadic Creutzfeldt-Jakob disease in Finland. Acta Neurol Scand 1993;87:469-474.
-
(1993)
Acta Neurol Scand
, vol.87
, pp. 469-474
-
-
Kovanen, J.1
-
33
-
-
0042422345
-
Diagnosis of new variant Creutzfeldt-Jakob disease
-
Will RG, Zeidler M, Stewart GE, et al. Diagnosis of new variant Creutzfeldt-Jakob disease. Ann Neurol 2000;47:575-582.
-
(2000)
Ann Neurol
, vol.47
, pp. 575-582
-
-
Will, R.G.1
Zeidler, M.2
Stewart, G.E.3
-
34
-
-
0036080558
-
Sensory features of variant Creutzfeldt-Jakob disease
-
Macleod M-A, Stewart GE, Zeidler M, et al. Sensory features of variant Creutzfeldt-Jakob disease. J Neurol 2002;249:706-711.
-
(2002)
J Neurol
, vol.249
, pp. 706-711
-
-
Macleod, M.-A.1
Stewart, G.E.2
Zeidler, M.3
-
35
-
-
0035962356
-
Variant Creutzfeldt-Jakob disease in an elderly patient
-
Lorains JW, Henry C, Agbamu DA, et al. Variant Creutzfeldt-Jakob disease in an elderly patient. Lancet 2001;357:1339-1340.
-
(2001)
Lancet
, vol.357
, pp. 1339-1340
-
-
Lorains, J.W.1
Henry, C.2
Agbamu, D.A.3
-
36
-
-
0036218622
-
Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests
-
Zerr I, Poser S. Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests. APMIS 2002;110:88-98.
-
(2002)
APMIS
, vol.110
, pp. 88-98
-
-
Zerr, I.1
Poser, S.2
-
37
-
-
0031588178
-
New variant Creutzfekh-Jakob disease: Neurological features and diagnostic tests
-
Zeidler M, Stewart GE, Barraclough CR, et al. New variant Creutzfekh-Jakob disease: neurological features and diagnostic tests. Lancet 1997;350:903-907.
-
(1997)
Lancet
, vol.350
, pp. 903-907
-
-
Zeidler, M.1
Stewart, G.E.2
Barraclough, C.R.3
-
38
-
-
14544301414
-
The neuropsychology of variant CJD: A comparative study with inherited and sporadic forms of prion disease
-
Cordery RJ, Alner K, Cipolotti L, et al. The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease. J Neurol Neurosurg Psychiatry 2005;76:330-336.
-
(2005)
J Neurol Neurosurg Psychiatry
, vol.76
, pp. 330-336
-
-
Cordery, R.J.1
Alner, K.2
Cipolotti, L.3
-
39
-
-
0033779818
-
Clinicopathological phenotype of codon 129 valine homozygote sporadic CJD
-
Kovács GG, Head MW, Bunn TJ. Clinicopathological phenotype of codon 129 valine homozygote sporadic CJD. Neuropathol Appl Neurobiol 2000;26:463-472.
-
(2000)
Neuropathol Appl Neurobiol
, vol.26
, pp. 463-472
-
-
Kovács, G.G.1
Head, M.W.2
Bunn, T.J.3
-
40
-
-
0036845856
-
Clinical findings in sporadic Creutzfeldt-Jakob disease correlate with thalamic pathology
-
Tschampa HJ, Herms JW, Schulz-Schaeffer WJ, et al. Clinical findings in sporadic Creutzfeldt-Jakob disease correlate with thalamic pathology. Brain 2002;125:2558-2566.
-
(2002)
Brain
, vol.125
, pp. 2558-2566
-
-
Tschampa, H.J.1
Herms, J.W.2
Schulz-Schaeffer, W.J.3
-
41
-
-
25444461293
-
Prion protein genotype in Creutzfeldt-Jakob disease: The Edinburgh experience
-
de Silva R, Windl O, Dempster M, et al. Prion protein genotype in Creutzfeldt-Jakob disease: the Edinburgh experience. Ann Neurol 1994;36:272.
-
(1994)
Ann Neurol
, vol.36
, pp. 272
-
-
De Silva, R.1
Windl, O.2
Dempster, M.3
-
43
-
-
0032585594
-
Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies
-
Johnson RT, Gibbs CJ Jr. Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies. N Engl J Med 1998;339:1994-2004.
-
(1998)
N Engl J Med
, vol.339
, pp. 1994-2004
-
-
Johnson, R.T.1
Gibbs Jr., C.J.2
-
44
-
-
0034991599
-
Severe brain atrophy in a case of thalamic variant of sporadic CJD with plaque-like PrP deposition
-
Yamashita M, Yamamoto T, Nishinaka K, et al. Severe brain atrophy in a case of thalamic variant of sporadic CJD with plaque-like PrP deposition. Neuropathology 2001;21:138-143.
-
(2001)
Neuropathology
, vol.21
, pp. 138-143
-
-
Yamashita, M.1
Yamamoto, T.2
Nishinaka, K.3
-
45
-
-
0034793570
-
Creutzfeldt-Jakob disease in unusually young patients who consumed venison
-
Belay E, Gambetti P, Lawrence B. Creutzfeldt-Jakob disease in unusually young patients who consumed venison. Arch Neurol 2001;58:1673-1678.
-
(2001)
Arch Neurol
, vol.58
, pp. 1673-1678
-
-
Belay, E.1
Gambetti, P.2
Lawrence, B.3
-
46
-
-
0024223734
-
Progressive neurological deterioration in a 14-year-old girl
-
Berman PH, Davidson GS, Becker LE. Progressive neurological deterioration in a 14-year-old girl. Pediatr Neurosci 1988;14:42-49.
-
(1988)
Pediatr Neurosci
, vol.14
, pp. 42-49
-
-
Berman, P.H.1
Davidson, G.S.2
Becker, L.E.3
-
48
-
-
0018824163
-
Creutzfeldt-Jakob disease in a 20-year-old woman
-
Packer RJ, Cornblath DR, Gonatas NK, et al. Creutzfeldt-Jakob disease in a 20-year-old woman. Neurology 1980;30:492-449.
-
(1980)
Neurology
, vol.30
, pp. 492-1449
-
-
Packer, R.J.1
Cornblath, D.R.2
Gonatas, N.K.3
-
49
-
-
0022405270
-
Epidemiologic implications of Cteutzfeldt-Jakob disease in a 19 year-old girl
-
Brown P, Cathala F, Labauge R, et al. Epidemiologic implications of Cteutzfeldt-Jakob disease in a 19 year-old girl. Eur J Epidemiol 1985;1:42-47.
-
(1985)
Eur J Epidemiol
, vol.1
, pp. 42-47
-
-
Brown, P.1
Cathala, F.2
Labauge, R.3
-
50
-
-
0034909904
-
Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: Atypical molecular phenotype
-
Head MW, Tissingh G, Uitdehaag BM, et al. Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotype. Ann Neurol 2001;50:258-261.
-
(2001)
Ann Neurol
, vol.50
, pp. 258-261
-
-
Head, M.W.1
Tissingh, G.2
Uitdehaag, B.M.3
-
52
-
-
0036902936
-
Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease
-
Snowden JS, Mann DMA, Neary D. Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry 2002;73:686-694.
-
(2002)
J Neurol Neurosurg Psychiatry
, vol.73
, pp. 686-694
-
-
Snowden, J.S.1
Mann, D.M.A.2
Neary, D.3
-
53
-
-
0032697989
-
Creutzfeldt-Jakob disease appearing as paranoid psychosis
-
Dunn NR, Alfonso CA, Young RA, et al. Creutzfeldt-Jakob disease appearing as paranoid psychosis. Am J Psychiatry 1999;156:2016-2017.
-
(1999)
Am J Psychiatry
, vol.156
, pp. 2016-2017
-
-
Dunn, N.R.1
Alfonso, C.A.2
Young, R.A.3
-
54
-
-
0038326556
-
Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease
-
Martindale J, Geschwind M, De Armond S, et al. Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease. Arch Neurol 2003;60:767-770.
-
(2003)
Arch Neurol
, vol.60
, pp. 767-770
-
-
Martindale, J.1
Geschwind, M.2
De Armond, S.3
-
55
-
-
0344942637
-
Clinical and radiological mimicry of vCJD in a valine homozygous PrP(Sc) type 1 sCJD patient
-
Rossetti AO, Glatzel M, Aguzzi A, et al. Clinical and radiological mimicry of vCJD in a valine homozygous PrP(Sc) type 1 sCJD patient. J Neurol 2003;250:491-493.
-
(2003)
J Neurol
, vol.250
, pp. 491-493
-
-
Rossetti, A.O.1
Glatzel, M.2
Aguzzi, A.3
|