-
1
-
-
20944445878
-
Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada
-
DOI 10.1212/01.WNL.0000160117.56690.B2
-
Ladogana A, Puopolo M, Croes EA, et al: Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology 2005; 64: 1586-1591. (Pubitemid 40617696)
-
(2005)
Neurology
, vol.64
, Issue.9
, pp. 1586-1591
-
-
Ladogana, A.1
Puopolo, M.2
Croes, E.A.3
Budka, H.4
Jarius, C.5
Collins, S.6
Klug, G.M.7
Sutcliffe, T.8
Giulivi, A.9
Alperovitch, A.10
Delasnerie-Laupretre, N.11
Brandel, J.-P.12
Poser, S.13
Kretzschmar, H.14
Rietveld, I.15
Mitrova, E.16
De Pedro Cuesta, J.17
Martinez-Martin, P.18
Glatzel, M.19
Aguzzi, A.20
Knight, R.21
Ward, H.22
Pocchiari, M.23
Van Duijn, C.M.24
Will, R.G.25
Zerr, I.26
more..
-
2
-
-
84855679278
-
Contribución al conocimiento de la degeneración corticoespinal o 'pseudoesclerosis espástica de Jakob'
-
Dimitri V, Aranovich J: Contribución al conocimiento de la degeneración corticoespinal o 'pseudoesclerosis espástica de Jakob'. Rev Neurol Arg 1945; 10: 225-228.
-
(1945)
Rev Neurol Arg
, vol.10
, pp. 225-228
-
-
Dimitri, V.1
Aranovich, J.2
-
4
-
-
0024894291
-
Creutzfeldt Jakob disease Report of 10 neuropathologically verified cases in Argentina
-
Taratuto AL, Piccardo P, Leiguarda R, et al: Creutzfeldt Jakob disease. Report of 10 neuropathologically verified cases in Argentina. Medicina 1989; 4: 293-303.
-
(1989)
Medicina
, vol.4
, pp. 293-303
-
-
Taratuto, A.L.1
Piccardo, P.2
Leiguarda, R.3
-
5
-
-
0030580788
-
WHO consultation on public health issues related to BSE and the emergence of a new variant of Creutzfeldt-Jakob disease
-
Bovine Spongiform Encephalopathy (BSE)
-
Bovine Spongiform Encephalopathy (BSE). WHO consultation on public health issues related to BSE and the emergence of a new variant of Creutzfeldt-Jakob disease. Wkly Epidemiol Rec 1996; 71: 113-115.
-
(1996)
Wkly Epidemiol Rec
, vol.71
, pp. 113-115
-
-
-
6
-
-
0037069259
-
Creutzfeldt-Jakob disease in Australia 1970-1999
-
Collins S, Boyd A, Lee JS, et al: Creutzfeldt- Jakob disease in Australia 1970-1999. Neurology 2002; 59: 1365-1371. (Pubitemid 35285988)
-
(2002)
Neurology
, vol.59
, Issue.9
, pp. 1365-1371
-
-
Collins, S.1
Boyd, A.2
Lee, J.S.3
Lewis, V.4
Fletcher, A.5
McLean, C.A.6
Law, M.7
Kaldor, J.8
Smith, M.J.9
Masters, C.L.10
-
7
-
-
22044441644
-
Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles
-
DOI 10.1212/01.wnl.0000167188.65787.a0
-
Lewis V, Hill AF, Klug GM, Boyd A, Masters CL, Collins SJ: Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles. Neurology 2005; 65: 113-118. (Pubitemid 40967785)
-
(2005)
Neurology
, vol.65
, Issue.1
, pp. 113-118
-
-
Lewis, V.1
Hill, A.F.2
Klug, G.M.3
Boyd, A.4
Masters, C.L.5
Collins, S.J.6
-
8
-
-
84888444743
-
-
OIE: Resolution XXI.I.
-
OIE: Resolution XXII. 2009. http://www.oie. int/esp/Status/BSE/es-BSE- free.htm.
-
(2009)
-
-
-
9
-
-
33646059507
-
Predicting susceptibility and incubation time of human-to-human transmission of vCJD
-
Bishop MT, Hart P, Aitchison L, et al: Predicting susceptibility and incubation time of human-to-human transmission of vCJD. Lancet Neurol 2006; 5: 393-398.
-
(2006)
Lancet Neurol
, vol.5
, pp. 393-398
-
-
Bishop, M.T.1
Hart, P.2
Aitchison, L.3
-
10
-
-
34249680730
-
Creutzfeldt-Jakob disease in Germany: A prospective 12-year surveillance
-
DOI 10.1093/brain/awm063
-
Heinemann U, Krasnianski A, Meissner B, et al: Creutzfeldt-Jakob disease in Germany: A prospective 12-year surveillance. Brain 2007; 130: 1350-1359. (Pubitemid 47355957)
-
(2007)
Brain
, vol.130
, Issue.5
, pp. 1350-1359
-
-
Heinemann, U.1
Krasnianski, A.2
Meissner, B.3
Varges, D.4
Kallenberg, K.5
Schulz-Schaeffer, W.J.6
Steinhoff, B.J.7
Grasbon-Frodl, E.M.8
Kretzschmar, H.A.9
Zerr, I.10
-
11
-
-
46749121818
-
A novel human disease with abnormal prion protein sensitive to protease
-
DOI 10.1002/ana.21420
-
Gambetti P, Dong Z, Yuan J, et al: A novel human disease with abnormal prion protein sensitive to protease. Ann Neurol 2008; 63: 697-708. (Pubitemid 351945529)
-
(2008)
Annals of Neurology
, vol.63
, Issue.6
, pp. 697-708
-
-
Gambetti, P.1
Dong, Z.2
Yuan, J.3
Xiao, X.4
Zheng, M.5
Alshekhlee, A.6
Castellani, R.7
Cohen, M.8
Barria, M.A.9
Gonzalez-Romero, D.10
Belay, E.D.11
Schonberger, L.B.12
Marder, K.13
Harris, C.14
Burke, J.R.15
Montine, T.16
Wisniewski, T.17
Dickson, D.W.18
Soto, C.19
Hulette, C.M.20
Mastrianni, J.A.21
Kong, Q.22
Zou, W.-Q.23
more..
-
12
-
-
45749093810
-
Creutzfeldt-Jakob disease in Austria: An autopsy- controlled study
-
Gelpi E, Heinzl H, Hoftberger R, et al: Creutzfeldt-Jakob disease in Austria: An autopsy- controlled study. Neuroepidemiology 2008; 30: 215-222.
-
(2008)
Neuroepidemiology
, vol.30
, pp. 215-222
-
-
Gelpi, E.1
Heinzl, H.2
Hoftberger, R.3
-
13
-
-
84888464671
-
-
World Health Organization, WHO Manual for Strengthening Diagnosis and Surveillance of Creutzfeldt-Jakob Disease Geneva, World Health Organization, Department of Surveillance and Response, Programme of Communicable Diseases 1998
-
World Health Organization: WHO Manual for Strengthening Diagnosis and Surveillance of Creutzfeldt-Jakob Disease. Geneva, World Health Organization, Department of Surveillance and Response, Programme of Communicable Diseases, 1998.
-
-
-
-
14
-
-
84355163730
-
-
World Health Organization: WHO Manual for Surveillance of Human Transmissible Spongiform Encephalopathies Including Variant Creutzfeldt-Jakob Disease. Geneva, World Health Organization
-
World Health Organization: WHO Manual for Surveillance of Human Transmissible Spongiform Encephalopathies Including Variant Creutzfeldt-Jakob Disease. Geneva, World Health Organization, 2003.
-
(2003)
-
-
-
15
-
-
4944246589
-
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
-
DOI 10.1093/brain/awh249
-
Pocchiari M, Puopolo M, Croes EA, et al: Predictors of survival in sporadic Creutzfeldt- Jakob disease and other human transmissible spongiform encephalopathies. Brain 2004; 127: 2348-2359. (Pubitemid 39382243)
-
(2004)
Brain
, vol.127
, Issue.10
, pp. 2348-2359
-
-
Pocchiari, M.1
Puopolo, M.2
Croes, E.A.3
Budka, H.4
Gelpi, E.5
Collins, S.6
Lewis, V.7
Sutcliffe, T.8
Guilivi, A.9
Delasnerie-Laupretre, N.10
Brandel, J.-P.11
Alperovitch, A.12
Zerr, I.13
Poser, S.14
Kretzschmar, H.A.15
Ladogana, A.16
Rietvald, I.17
Mitrova, E.18
Martinez-Martin, P.19
De Pedro-Cuesta, J.20
Glatzel, M.21
Aguzzi, A.22
Cooper, S.23
Mackenzie, J.24
Van Duijn, C.M.25
Will, R.G.26
more..
-
16
-
-
0030056269
-
Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease
-
Steinhoff BJ, Räcker 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
Räcker, S.2
Herrendorf, G.3
-
17
-
-
9144221019
-
Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease
-
DOI 10.1002/ana.20261
-
Steinhoff BJ, Zerr I, Glatting M, Schulz- Schaeffer W, Poser S, Kretzschmar HA: Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease. Ann Neurol 2004; 56: 702-708. (Pubitemid 39540751)
-
(2004)
Annals of Neurology
, vol.56
, Issue.5
, pp. 702-708
-
-
Steinhoff, B.J.1
Zerr, I.2
Glatting, M.3
Schulz-Schaeffer, W.4
Poser, S.5
Kretzschmar, H.A.6
-
18
-
-
0035453360
-
MRI of Creutzfeldt-Jakob disease: Imaging features and recommended MRI protocol
-
DOI 10.1053/crad.2001.0771
-
Collie DA, Sellar RJ, Zeidler M, Colchester AC, Knight R, Will RG: MRI of Creutzfeldt- Jakob disease: Imaging features and recommended MRI protocol. Clin Radiol 2001; 56: 726-739. (Pubitemid 35023797)
-
(2001)
Clinical Radiology
, vol.56
, Issue.9
, 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
-
19
-
-
33747517258
-
Creutzfeldt-Jakob disease: Comparative analysis of MR imaging sequences
-
Kallenberg K, Schulz Schafer W, Jastrow U, Poser S, Meissner B, Tschampa H, et al: Creutzfeldt-Jakob disease. Comparative analysis of MRI imaging sequences. Am J Neuroradiol 2006; 27: 1459-1462. (Pubitemid 44260128)
-
(2006)
American Journal of Neuroradiology
, vol.27
, Issue.7
, pp. 1459-1462
-
-
Kallenberg, K.1
Schulz-Schaeffer, W.J.2
Jastrow, U.3
Poser, S.4
Meissner, B.5
Tschampa, H.J.6
Zerr, I.7
Knauth, M.8
-
20
-
-
0031914675
-
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
-
DOI 10.1002/ana.410430109
-
Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Witfang J, 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. (Pubitemid 28124646)
-
(1998)
Annals of Neurology
, vol.43
, Issue.1
, pp. 32-40
-
-
Zerr, I.1
Bodemer, M.2
Gefeller, O.3
Otto, M.4
Poser, S.5
Wiltfang, J.6
Windl, O.7
Kretzschmar, H.A.8
Weber, T.9
-
21
-
-
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
-
22
-
-
0028876473
-
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)
-
Budka H, Aguzzi A, Brown P, et al: Neuropathological diagnostic criteria for Creutzfeldt- Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995; 5: 459-466.
-
(1995)
Brain Pathol
, vol.5
, pp. 459-466
-
-
Budka, H.1
Aguzzi, A.2
Brown, P.3
-
23
-
-
0029741936
-
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease
-
Kretschmar HA, Ironside JW, De Armond SJ, Tateishi J: Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch Neurol 1996; 53: 913-920. (Pubitemid 26301703)
-
(1996)
Archives of Neurology
, vol.53
, Issue.9
, pp. 913-920
-
-
Kretzschmar, H.A.1
Ironside, J.W.2
DeArmond, S.J.3
Tateishi, J.4
-
24
-
-
8044239656
-
Prion protein immunocytochemistry - UK five centre consensus report
-
Bell JE, Gentleman SM, Ironside JW, et al: Prion protein immunocytochemistry - UK five centre consensus report. Neuropathol Appl Neurobiol 1997; 23: 26-35. (Pubitemid 27081214)
-
(1997)
Neuropathology and Applied Neurobiology
, vol.23
, Issue.1
, pp. 26-35
-
-
Bell, J.E.1
Gentleman, S.M.2
Ironside, J.W.3
McCardle, L.4
Lantos, P.L.5
Doey, L.6
Lowe, J.7
Fergusson, J.8
Luthert, P.9
McQuaid, S.10
Allen, I.V.11
-
25
-
-
0036132894
-
Immunohistochemistry of the prion protein: Comparison of different monoclonal antibodies in human prion disease subtypes
-
Kovacs GG, Head MW, Hegy I, et al: Immunohistochemistry of the prion protein: Comparison of different monoclonal antibodies in human prion disease subtypes. Brain Pathol 2000; 12: 1-11.
-
(2000)
Brain Pathol
, vol.12
, pp. 1-11
-
-
Kovacs, G.G.1
Head, M.W.2
Hegy, I.3
-
26
-
-
0141849861
-
Neuropathology of prion diseases
-
DOI 10.1093/bmb/66.1.121
-
Budka H: Neuropathology of prion diseases. Br Med Bull 2003; 66: 121-130. (Pubitemid 37173497)
-
(2003)
British Medical Bulletin
, vol.66
, pp. 121-130
-
-
Budka, H.1
-
28
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
-
DOI 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
-
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. (Pubitemid 29382879)
-
(1999)
Annals of Neurology
, vol.46
, Issue.2
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
Brown, P.4
Schulz-Schaeffer, W.5
Windl, O.6
Zerr, I.7
Budka, H.8
Kopp, N.9
Piccardo, P.10
Poser, S.11
Rojiani, A.12
Streichemberger, N.13
Julien, J.14
Vital, C.15
Ghetti, B.16
Gambetti, P.17
Kretzschmar, H.18
-
29
-
-
0026406817
-
A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin
-
Korczyn AD, Chapman J, Goldfarb LG, Brown P, Gajdusek DC: A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin. Ann NY Acad Sci 1991; 640: 171-176.
-
(1991)
Ann NY Acad Sci
, vol.640
, pp. 171-176
-
-
Korczyn, A.D.1
Chapman, J.2
Goldfarb, L.G.3
Brown, P.4
Gajdusek, D.C.5
-
30
-
-
0025918142
-
Creutzfeldt-Jakob disease associated with the PRNP codon 200Lys mutation: An analysis of 45 families
-
Goldfarb LG, Brown P, Mitrova E, et al: Creutzfeldt-Jakob disease associated with the PRNP codon 200Lys mutation: An analysis of 45 families. Eur J Epidemiol 1991; 7: 477-486.
-
(1991)
Eur J Epidemiol
, vol.7
, pp. 477-486
-
-
Goldfarb, L.G.1
Brown, P.2
Mitrova, E.3
-
31
-
-
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, Gálvez S, Goldfarb LG, et al: 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 1992; 112: 65-67.
-
(1992)
J Neurol Sci
, vol.112
, pp. 65-67
-
-
Brown, P.1
Gálvez, S.2
Goldfarb, L.G.3
-
32
-
-
84888457877
-
-
Instituto Nacional de Estadística y Censos
-
Instituto Nacional de Estadística y Censos. http:// www.indec.gov.ar.
-
-
-
-
33
-
-
0037065769
-
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease
-
Taratuto AL, Piccardo P, Reich F, et al: Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology 2002; 58: 362-367. (Pubitemid 34150908)
-
(2002)
Neurology
, vol.58
, Issue.3
, pp. 362-367
-
-
Taratuto, A.L.1
Piccardo, P.2
Reich, E.G.3
Chen, S.G.4
Sevlever, G.5
Schultz, M.6
Luzzi, A.A.7
Rugiero, M.8
Abecasis, G.9
Endelman, M.10
Garcia, A.M.11
Capellari, S.12
Xie, Z.13
Lugaresi, E.14
Gambetti, P.15
Dlouhy, S.R.16
Ghetti, B.17
-
34
-
-
16644393112
-
Creutzfeldt-Jakob encephalopathy with mutation E200K Report of a 'sporadic' case
-
Cosacov RM, Taratuto AL, Ghirardi G, et al: Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a 'sporadic' case. Rev Fac Cien Med Univ Nac Cordoba 2004; 61: 48-53.
-
(2004)
Rev Fac Cien Med Univ Nac Cordoba
, vol.61
, pp. 48-53
-
-
Cosacov, R.M.1
Taratuto, A.L.2
Ghirardi, G.3
-
35
-
-
0018231481
-
Epidemiology of CJD in the Paris area
-
Cathala F, Brown P, Buge A, Lhermitte F, Castaigne P, Gajdusek DC: Epidemiology of CJD in the Paris area. Rev Neurol (Paris) 1978; 134: 741-750.
-
(1978)
Rev Neurol (Paris)
, vol.134
, pp. 741-750
-
-
Cathala, F.1
Brown, P.2
Buge, A.3
Lhermitte, F.4
Castaigne, P.5
Gajdusek, D.C.6
-
36
-
-
0018360851
-
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
-
DOI 10.1002/ana.410050212
-
Masters CL, Harris JO, Gajdusek DC, Gibbs CJ Jr, Bernoulli C, Asher DM: Patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 1979; 5: 177-188. (Pubitemid 9195818)
-
(1979)
Annals of Neurology
, vol.5
, Issue.2
, pp. 177-188
-
-
Masters, C.1
Harris, J.O.2
Gajdusek, D.C.3
-
37
-
-
0020563063
-
Correlation between population density and the frequency of Creutzfeldt-Jakob disease in France
-
DOI 10.1016/0022-510X(83)90136-3
-
Brown P, Cathala F, Sadowsky D: Correlation between population density and the frequency of Creutzfeldt-Jakob disease in France. J Neurol Sci 1983; 60: 169-176. (Pubitemid 13055169)
-
(1983)
Journal of the Neurological Sciences
, vol.60
, Issue.1
, pp. 169-176
-
-
Brown, P.1
Cathala, F.2
Sadowsky, D.3
-
38
-
-
0018834536
-
Descriptive epidemiology of Creutzfeldt-Jakob disease in Chile
-
Gálvez S, Masters C, Gajdusek C: Descriptive epidemiology of Creutzfeldt-Jakob disease in Chile. Arch Neurol 1980; 37: 11-14. (Pubitemid 10160402)
-
(1980)
Archives of Neurology
, vol.37
, Issue.1
, pp. 11-14
-
-
Galvez, S.1
Masters, C.2
Gajdusek, D.C.3
-
39
-
-
10444275898
-
A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: Analysis of clustering
-
Linsell L, Cousens SN, Smith PG, et al: A case-control study of sporadic Creutzfeldt- Jakob disease in the United Kingdom: Analysis of clustering. Neurology 2004; 63: 2077-2083. (Pubitemid 39636255)
-
(2004)
Neurology
, vol.63
, Issue.11
, pp. 2077-2083
-
-
Linsell, L.1
Cousens, S.N.2
Smith, P.G.3
Knight, R.S.G.4
Zeidler, M.5
Stewart, G.6
De Silva, R.7
Esmonde, T.F.G.8
Ward, H.J.T.9
Will, R.G.10
-
40
-
-
60149101706
-
Enhanced geographically restricted surveillance simulates CJD cluster
-
Klug GM, Wand H, Boyd A, et al: Enhanced geographically restricted surveillance simulates CJD cluster. Brain 2009; 132: 493-501.
-
(2009)
Brain
, vol.132
, pp. 493-501
-
-
Klug, G.M.1
Wand, H.2
Boyd, A.3
-
41
-
-
0027443351
-
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation
-
Chapman J, Brown P, Golfarb LG, et al: Clinical heterogeneity and unusual presentation of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. J Neurol Neurosurg Psychiatry 1993; 56: 1109-1112. (Pubitemid 23304704)
-
(1993)
Journal of Neurology Neurosurgery and Psychiatry
, vol.56
, Issue.10
, pp. 1109-1112
-
-
Chapman, J.1
Brown, P.2
Goldfarb, L.G.3
Arlazoroff, A.4
Gajdusek, D.C.5
Korczyn, A.D.6
-
42
-
-
0342505312
-
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
-
DOI 10.1086/302340
-
Lee HS, Sambuughin N, Cervenakova L, et al: Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. Am J Hum Genet 1999; 64: 1063-1070. (Pubitemid 30463037)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.4
, pp. 1063-1070
-
-
Lee, H.S.1
Sambuughin, N.2
Cervenakova, L.3
Chapman, J.4
Pocchiari, M.5
Litvak, S.6
Qi, H.Y.7
Budka, H.8
Del Ser, T.9
Furukawa, H.10
Brown, P.11
Gajdusek, D.C.12
Long, J.C.13
Korczyn, A.D.14
Goldfarb, L.G.15
-
43
-
-
84888446138
-
-
http://www.worldlifeexpectancy.com/history- of-life-expectancy
-
-
-
-
44
-
-
0036100049
-
Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998
-
d'Aignaux JH, Cousens SN, Delasnerie-Lauprêtre, et al: Analysis or the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998. Int J Epidemiol 2002; 31: 490-495. (Pubitemid 34537820)
-
(2002)
International Journal of Epidemiology
, vol.31
, Issue.2
, pp. 490-495
-
-
D'Aignaux, J.H.1
Cousens, S.N.2
Delasnerie-Laupretre, N.3
Brandel, J.-P.4
Salomon, D.5
Laplanche, J.-L.6
Hauw, J.-J.7
Alperovitch, A.8
-
45
-
-
33749236229
-
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease
-
DOI 10.1093/brain/awl159
-
Collins SJ, Sanchez-Juan P, Masters CL, et al: Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain 2006; 129: 2278-2287. (Pubitemid 44522114)
-
(2006)
Brain
, vol.129
, Issue.9
, pp. 2278-2287
-
-
Collins, S.J.1
Sanchez-Juan, P.2
Masters, C.L.3
Klug, G.M.4
Van Duijn, C.5
Poleggi, A.6
Pocchiari, M.7
Almonti, S.8
Cuadrado-Corrales, N.9
De Pedro-Cuesta, J.10
Budka, H.11
Gelpi, E.12
Glatzel, M.13
Tolnay, M.14
Hewer, E.15
Zerr, I.16
Heinemann, U.17
Kretszchmar, H.A.18
Jansen, G.H.19
Olsen, E.20
Mitrova, E.21
Alperovitch, A.22
Brandel, J.-P.23
Mackenzie, J.24
Murray, K.25
Will, R.G.26
more..
-
46
-
-
34547098122
-
Creutzfeldt-Jakob disease mortality in Japan, 1979-2004: Analysis of national death certificate data
-
Doi Y, Yokoyama T; Sakai M, Nakamura Y: Creutzfeldt-Jakob disease mortality in Japan, 1979-2004: Analysis of national death certificate data. J Epidemiol 2007; 17: 133-139.
-
(2007)
J Epidemiol
, vol.17
, pp. 133-139
-
-
Doi, Y.1
Yokoyama, T.2
Sakai, M.3
Nakamura, Y.4
-
47
-
-
84888452610
-
-
INDEC: Encuesta Complementaria de Pueblos Indígenas (ECPI)
-
INDEC: Encuesta Complementaria de Pueblos Indígenas (ECPI) 2004-2005. http:// www.indec.mecon.ar/nuevaweb/cuadros/2/ ECPI-res-generales- junio2006.pdf.
-
(2004)
-
-
-
48
-
-
70049114839
-
14-3-3 CSF levels in sporadic Creutzfeldt- Jakob disease differ across molecular subtypes
-
Gmitterová K, Heinemann U, Bodemer M, et al: 14-3-3 CSF levels in sporadic Creutzfeldt- Jakob disease differ across molecular subtypes. Neurobiol Aging 2009; 30: 1842-1850.
-
(2009)
Neurobiol Aging
, vol.30
, pp. 1842-1850
-
-
Gmitterová, K.1
Heinemann, U.2
Bodemer, M.3
-
49
-
-
70349947005
-
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
-
Zerr I, Kallenberg K, Summers DM, et al: Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain 2009; 132: 2659-2668.
-
(2009)
Brain
, vol.132
, pp. 2659-2668
-
-
Zerr, I.1
Kallenberg, K.2
Summers, D.M.3
-
50
-
-
46749121818
-
A novel human disease with abnormal prion protein sensitive to protease
-
DOI 10.1002/ana.21420
-
Gambetti P, Dong Z, Yuan J, et al: A novel human disease with abnormal prion protein sensitive to protease. Ann Neurol 2008; 63: 697-708. (Pubitemid 351945529)
-
(2008)
Annals of Neurology
, vol.63
, Issue.6
, pp. 697-708
-
-
Gambetti, P.1
Dong, Z.2
Yuan, J.3
Xiao, X.4
Zheng, M.5
Alshekhlee, A.6
Castellani, R.7
Cohen, M.8
Barria, M.A.9
Gonzalez-Romero, D.10
Belay, E.D.11
Schonberger, L.B.12
Marder, K.13
Harris, C.14
Burke, J.R.15
Montine, T.16
Wisniewski, T.17
Dickson, D.W.18
Soto, C.19
Hulette, C.M.20
Mastrianni, J.A.21
Kong, Q.22
Zou, W.-Q.23
more..
-
51
-
-
77955302607
-
Variably protease - sensitive prionopathy: A new sporadic disease of the prion protein
-
Zou W-Q, Puoti G, Xiao X, et al: Variably protease - sensitive prionopathy: A new sporadic disease of the prion protein. Ann Neurol 2010; 68: 162-172.
-
(2010)
Ann Neurol
, vol.68
, pp. 162-172
-
-
Zou, W.-Q.1
Puoti, G.2
Xiao, X.3
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