-
1
-
-
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. Annals of Neurology 1996; 39: 767-778.
-
(1996)
Annals of Neurology
, vol.39
, pp. 767-778
-
-
Parchi, P.1
Castellani, R.2
Capellari, S.3
-
2
-
-
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. Annals of Neurology 1999; 46: 224-233.
-
(1999)
Annals of Neurology
, vol.46
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
-
3
-
-
3543049532
-
Sensitivity of 14-33 protein test varies in subtypes of sporadic Creutzfeldt - Jakob disease
-
Castellani RJ, Colucci M, Xie Z, et al. Sensitivity of 14-33 protein test varies in subtypes of sporadic Creutzfeldt - Jakob disease. Neurology 2004; 63: 436-442.
-
(2004)
Neurology
, vol.63
, pp. 436-442
-
-
Castellani, R.J.1
Colucci, M.2
Xie, Z.3
-
4
-
-
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. Annals of Neurology 2000; 48: 323-329.
-
(2000)
Annals of Neurology
, vol.48
, pp. 323-329
-
-
Zerr, I.1
Schulz-Schaeffer, W.J.2
Giese, A.3
-
5
-
-
33749237508
-
Clinical findings and diagnostic tests in the MV-2 subtype of sporadic CJD
-
Krasnianski A, Schulz-Schaeffer WJ, Kallenberg K, et al. Clinical findings and diagnostic tests in the MV-2 subtype of sporadic CJD. Brain 2006; 129: 2288-2296.
-
(2006)
Brain
, vol.129
, pp. 2288-2296
-
-
Krasnianski, A.1
Schulz-Schaeffer, W.J.2
Kallenberg, K.3
-
6
-
-
0026808879
-
Pulsatile brain movement and associated hydrodynamics studied by magnetic resonance phase imaging. The Monro-Kellie doctrine revisited
-
Greitz D, Wirestam R, Franck A, Nordell B, Thomsen C, Stahlberg F. Pulsatile brain movement and associated hydrodynamics studied by magnetic resonance phase imaging. The Monro-Kellie doctrine revisited. Neuroradiology 1992; 34: 370-380.
-
(1992)
Neuroradiology
, vol.34
, pp. 370-380
-
-
Greitz, D.1
Wirestam, R.2
Franck, A.3
Nordell, B.4
Thomsen, C.5
Stahlberg, F.6
-
7
-
-
0030731550
-
Brain magnetic resonance diffusion abnormalities in Creutzfeldt - Jakob disease
-
Bahn MM, Kido DK, Lin W, Pearlman AL. Brain magnetic resonance diffusion abnormalities in Creutzfeldt - Jakob disease. Archives of Neurology 1997; 54: 1411-1415.
-
(1997)
Archives of Neurology
, vol.54
, pp. 1411-1415
-
-
Bahn, M.M.1
Kido, D.K.2
Lin, W.3
Pearlman, A.L.4
-
8
-
-
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
-
9
-
-
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
-
12
-
-
32944463783
-
Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: High sensitivity and specificity for diagnosis
-
Young GS, Geschwind MD, Fischbein NJ, et al. Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis. American Journal of Neuroradiology 2005; 26: 1551-1562.
-
(2005)
American Journal of Neuroradiology
, vol.26
, pp. 1551-1562
-
-
Young, G.S.1
Geschwind, M.D.2
Fischbein, N.J.3
-
13
-
-
24344453861
-
et al.MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: A study on inter-observer agreement
-
Tschampa HJ, Kallenberg K, Urbach H, et al.MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: a study on inter-observer agreement. Brain 2005; 128(Pt 9): 2026-2033.
-
(2005)
Brain
, vol.128
, Issue.PART 9
, pp. 2026-2033
-
-
Tschampa, H.J.1
Kallenberg, K.2
Urbach, H.3
-
14
-
-
0034718472
-
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutz - feldt-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 Creutz - feldt-Jakob disease. Neurology 2000; 55: 811-815.
-
(2000)
Neurology
, vol.55
, pp. 811-815
-
-
Zerr, I.1
Pocchiari, M.2
Collins, S.3
-
15
-
-
0032553667
-
Human transmissible spongiform encephalopathies
-
WHO
-
WHO. Human transmissible spongiform encephalopathies. Weekly Epidemiological Record 1998; 47: 361-365.
-
(1998)
Weekly Epidemiological Record
, vol.47
, pp. 361-365
-
-
-
16
-
-
0030056269
-
Accuracy and reliability of periodic sharp wave complexes in Cre - utzfeldt-Jakob disease
-
Steinhoff BJ, Räcker S, Herrendorf G, et al. Accuracy and reliability of periodic sharp wave complexes in Cre - utzfeldt-Jakob disease. Archives of Neurology 1996; 53: 162-166.
-
(1996)
Archives of Neurology
, vol.53
, pp. 162-166
-
-
Steinhoff, B.J.1
Räcker, S.2
Herrendorf, G.3
-
17
-
-
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. Annals of Neurology 1998; 43:32-40.
-
(1998)
Annals of Neurology
, vol.43
, pp. 32-40
-
-
Zerr, I.1
Bodemer, M.2
Gefeller, O.3
-
18
-
-
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. The American Journal of Pathology 1992; 140: 1285-1294.
-
(1992)
The American Journal of Pathology
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.W.2
Doh-Ura, K.3
-
20
-
-
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. The American Journal of Pathology 2000; 156: 51-56.
-
(2000)
The American Journal of Pathology
, vol.156
, pp. 51-56
-
-
Schulz-Schaeffer, W.J.1
Tschoke, S.2
Kranefuss, N.3
-
21
-
-
0032843132
-
Molecular genetics of human prion diseases in Germany
-
Windl O, Giese A, Schulz-Schaeffer W, et al. Molecular genetics of human prion diseases in Germany. Human Genetics 1999; 105: 244-252.
-
(1999)
Human Genetics
, vol.105
, pp. 244-252
-
-
Windl, O.1
Giese, A.2
Schulz-Schaeffer, W.3
-
22
-
-
33746918622
-
MR intensity analysis to discriminate variant, sporadic CJD, and non-CJD dementia patients
-
Colchester ACF, Hojjat SA, Zerr I, Collie DA. MR intensity analysis to discriminate variant, sporadic CJD, and non-CJD dementia patients. Journal of Neurology, Neurosurgery, and Psychiatry 2004; 75: 41.
-
(2004)
Journal of Neurology, Neurosurgery, and Psychiatry
, vol.75
, pp. 41
-
-
Colchester, A.C.F.1
Hojjat, S.A.2
Zerr, I.3
Collie, D.A.4
-
23
-
-
33746927953
-
Differentiation of sCJD and vCJD forms by automated analysis of basal ganglia intensity distribution in multisequence MRI of the brain - definition and evaluation of new MRI-based ratios
-
Linguraru MG, Ayache N, Bardinet E, et al. Differentiation of sCJD and vCJD forms by automated analysis of basal ganglia intensity distribution in multisequence MRI of the brain - definition and evaluation of new MRI-based ratios. IEEE Transactions on Medical Imaging 2006; 25: 1052-1067.
-
(2006)
IEEE Transactions on Medical Imaging
, vol.25
, pp. 1052-1067
-
-
Linguraru, M.G.1
Ayache, N.2
Bardinet, E.3
-
24
-
-
28044438694
-
Sporadic Creutzfeldt-Jakob disease: Clinical and diagnostic characteristics of the rare VV1 type
-
Meissner B, Westner I, Kallenberg K, et al. Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type. Neurology 2005; 65: 1544-1550.
-
(2005)
Neurology
, vol.65
, pp. 1544-1550
-
-
Meissner, B.1
Westner, I.2
Kallenberg, K.3
-
25
-
-
27944483780
-
Genetic prion disease: The EUROCJD experience
-
Kovacs GG, Puopolo M, Ladogana A, et al. Genetic prion disease: the EUROCJD experience. Human Genetics 2005; 118: 166-174.
-
(2005)
Human Genetics
, vol.118
, pp. 166-174
-
-
Kovacs, G.G.1
Puopolo, M.2
Ladogana, A.3
-
26
-
-
0035453360
-
MRI of Creutzfeldt-Jakob disease: Imaging features and recommended MRI protocol
-
Collie DA, Sellar RJ, Zeidler M, Colchester ACF, Knight R, Will RG. MRI of Creutzfeldt-Jakob disease: imaging features and recommended MRI protocol. Clinical Radiology 2001; 56: 726-739.
-
(2001)
Clinical Radiology
, vol.56
, pp. 726-739
-
-
Collie, D.A.1
Sellar, R.J.2
Zeidler, M.3
Colchester, A.C.F.4
Knight, R.5
Will, R.G.6
-
27
-
-
1842475846
-
False-positive pulvinar sign on MRI in sporadic Creutzfeldt-Jakob disease
-
Petzold GC, Westner I, Bohner G, Einhäupl KN, Kretzschmar H, Valdueza JN. False-positive pulvinar sign on MRI in sporadic Creutzfeldt-Jakob disease. Neurology 2004; 62: 1235-1236.
-
(2004)
Neurology
, vol.62
, pp. 1235-1236
-
-
Petzold, G.C.1
Westner, I.2
Bohner, G.3
Einhäupl, K.N.4
Kretzschmar, H.5
Valdueza, J.N.6
-
28
-
-
0036266988
-
Prion protein deposits match magnetic resonance imaging signal abnormalities in Creutzfeldt-Jakob disease
-
Haik S, Dormont D, Faucheux BA, Marsault C, Hauw JJ. Prion protein deposits match magnetic resonance imaging signal abnormalities in Creutzfeldt-Jakob disease. Annals ofNeurology 2002; 51: 797-799.
-
(2002)
Annals ofNeurology
, vol.51
, pp. 797-799
-
-
Haik, S.1
Dormont, D.2
Faucheux, B.A.3
Marsault, C.4
Hauw, J.J.5
-
29
-
-
0344942637
-
Clinical and radiological mimicry of vCJD in a valine homozygous PrP(Sc) type 1 sCJD patient
-
Rossetti AO, Glatzel M, Aguzzi A, Janzer R, Bogous - slavsky J. Clinical and radiological mimicry of vCJD in a valine homozygous PrP(Sc) type 1 sCJD patient. Journal of Neurology 2003; 250: 491-493.
-
(2003)
Journal of Neurology
, vol.250
, pp. 491-493
-
-
Rossetti, A.O.1
Glatzel, M.2
Aguzzi, A.3
Janzer, R.4
Bogous5
slavsky, J.6
-
30
-
-
1542407288
-
MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrP type 2 in Japan
-
Fukushima R, Shiga Y, Nakamura M, Fujimori J, Kit - amato T, Yoshida Y. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrP type 2 in Japan. Journal ofNeurol - ogy, Neurosurgery, and Psychiatry 2004; 75: 485-487.
-
(2004)
Journal ofNeurol - ogy, Neurosurgery, and Psychiatry
, vol.75
, pp. 485-487
-
-
Fukushima, R.1
Shiga, Y.2
Nakamura, M.3
Fujimori, J.4
Kit5
amato, T.6
Yoshida, Y.7
-
31
-
-
0038326556
-
Sporadic Creutzfeldt-Jakob disease mimicking variant Cre - utzfeldt-Jakob disease
-
Martindale J, Geschwind M, De Armond S, et al. Sporadic Creutzfeldt-Jakob disease mimicking variant Cre - utzfeldt-Jakob disease. Archives ofNeurology 2003; 60: 767-770.
-
(2003)
Archives ofNeurology
, vol.60
, pp. 767-770
-
-
Martindale, J.1
Geschwind, M.2
De Armond, S.3
|