-
1
-
-
1842644947
-
Inherited prion diseases
-
2nd edition. Edited by: Prusiner SB. City: Cold Spring Harbor Laboratory Press
-
Kong Q, Surewicz WK, Petersen RB, et al.: Inherited prion diseases. In Prion Biology and Diseases. 2nd edition. Edited by: Prusiner SB. City: Cold Spring Harbor Laboratory Press; 2004:673-775.
-
(2004)
Prion Biology and Diseases
, pp. 673-775
-
-
Kong, Q.1
Surewicz, W.K.2
Petersen, R.B.3
-
2
-
-
0141514771
-
Sporadic and familial CJD: classification and characterisation
-
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG: Sporadic and familial CJD: classification and characterisation. Br Med Bull 2003, 66: 213-239. 10.1093/bmb/66.1.213
-
(2003)
Br Med Bull
, vol.66
, pp. 213-239
-
-
Gambetti, P.1
Kong, Q.2
Zou, W.3
Parchi, P.4
Chen, S.G.5
-
3
-
-
0024467653
-
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker's syndrome
-
Goldgaber D, Goldfarb LG, Brown P, et al.: Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker's syndrome. Exp Neurol 1989, 106: 204-206. 10.1016/0014-4886(89)90095-2
-
(1989)
Exp Neurol
, vol.106
, pp. 204-206
-
-
Goldgaber, D.1
Goldfarb, L.G.2
Brown, P.3
-
4
-
-
0342505312
-
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
-
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. 10.1086/302340
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1063-1070
-
-
Lee, H.S.1
Sambuughin, N.2
Cervenakova, L.3
-
5
-
-
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 N Y Acad Sci 1991, 640: 171-176.
-
(1991)
Ann N Y 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
-
6
-
-
27944483780
-
Genetic prion disease: the EUROCJD experience
-
Kovacs GG, Puopolo M, Ladogana A, et al.: Genetic prion disease: the EUROCJD experience. Hum Genet 2005, 118: 166-174. 10.1007/s00439-005-0020-1
-
(2005)
Hum Genet
, vol.118
, pp. 166-174
-
-
Kovacs, G.G.1
Puopolo, M.2
Ladogana, A.3
-
7
-
-
0036459944
-
Mutations of the prion protein gene phenotypic spectrum
-
Kovacs GG, Trabattoni G, Hainfellner JA, Ironside JW, Knight RS, Budka H: Mutations of the prion protein gene phenotypic spectrum. J Neurol 2002, 249: 1567-1582. 10.1007/s00415-002-0896-9
-
(2002)
J Neurol
, vol.249
, pp. 1567-1582
-
-
Kovacs, G.G.1
Trabattoni, G.2
Hainfellner, J.A.3
Ironside, J.W.4
Knight, R.S.5
Budka, H.6
-
8
-
-
0035996287
-
Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development
-
Mitrova E, Belay G: Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Acta Virol 2002, 46: 31-39.
-
(2002)
Acta Virol
, vol.46
, pp. 31-39
-
-
Mitrova, E.1
Belay, G.2
-
9
-
-
0025869213
-
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
-
Hsiao K, Meiner Z, Kahana E, et al.: Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. N Engl J Med 1991, 324: 1091-1097. 10.1056/NEJM199104183241604
-
(1991)
N Engl J Med
, vol.324
, pp. 1091-1097
-
-
Hsiao, K.1
Meiner, Z.2
Kahana, E.3
-
10
-
-
0031183207
-
Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews
-
Meiner Z, Gabizon R, Prusiner SB: Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews. Medicine (Baltimore) 1997, 76: 227-237. 10.1097/00005792-199707000-00001
-
(1997)
Medicine (Baltimore)
, vol.76
, pp. 227-237
-
-
Meiner, Z.1
Gabizon, R.2
Prusiner, S.B.3
-
11
-
-
13344295093
-
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP
-
Ghetti B, Piccardo P, Spillantini MG, et al.: Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. Proc Natl Acad Sci USA 1996, 93: 744-748. 10.1073/pnas.93.2.744
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 744-748
-
-
Ghetti, B.1
Piccardo, P.2
Spillantini, M.G.3
-
12
-
-
49849091894
-
Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease
-
Debatin L, Streffer J, Geissen M, Matschke J, Aguzzi A, Glatzel M: Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease. Neurodegener Dis 2008, 5: 347-354. doi: 10.1159/000121389 10.1159/000121389
-
(2008)
Neurodegener Dis
, vol.5
, pp. 347-354
-
-
Debatin, L.1
Streffer, J.2
Geissen, M.3
Matschke, J.4
Aguzzi, A.5
Glatzel, M.6
-
13
-
-
70350450945
-
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype
-
Ghoshal N, Cali I, Perrin RJ, et al.: Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype. Arch Neurol 2009, 66: 1240-1246.
-
(2009)
Arch Neurol
, vol.66
, pp. 1240-1246
-
-
Ghoshal, N.1
Cali, I.2
Perrin, R.J.3
-
14
-
-
78651257339
-
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy
-
Kovacs GG, Seguin J, I Q, et al.: Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Acta Neuropathol 2011, 121: 39-57. doi: 10.1007/s00401-010-0713-y 10.1007/s00401-010-0713-y
-
(2011)
Acta Neuropathol
, vol.121
, pp. 39-57
-
-
Kovacs, G.G.1
Seguin, J.I.Q.2
-
15
-
-
68249146549
-
The nigrostriatal pathway in Creutzfeldt-Jakob disease
-
Vital A, Fernagut PO, Canron MH, et al.: The nigrostriatal pathway in Creutzfeldt-Jakob disease. J Neuropathol Exp Neurol 2009, 68: 809-815. doi: 10.1097/NEN.0b013e3181abdae8 10.1097/NEN.0b013e3181abdae8
-
(2009)
J Neuropathol Exp Neurol
, vol.68
, pp. 809-815
-
-
Vital, A.1
Fernagut, P.O.2
Canron, M.H.3
-
16
-
-
84870337113
-
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease
-
Carswell C, Thompson A, A L, et al.: MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease. BMC Neurol 2012, 12: 153. doi: 10.1186/1471-2377-12-153 10.1186/1471-2377-12-153
-
(2012)
BMC Neurol
, vol.12
, pp. 153
-
-
Carswell, C.1
Thompson, A.A.L.2
-
17
-
-
0033853890
-
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation
-
Puoti G, Rossi G, G G, et al.: Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation. Ann Neurol 2000, 48: 269-270.
-
(2000)
Ann Neurol
, vol.48
, pp. 269-270
-
-
Puoti, G.1
Rossi, G.G.G.2
-
18
-
-
62949172413
-
Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease
-
Geschwind MD, Potter CA, Sattavat M, et al.: Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease. Alzheimer Dis Assoc Disord 2009, 23: 82-87. 10.1097/WAD.0b013e31818323ef
-
(2009)
Alzheimer Dis Assoc Disord
, vol.23
, pp. 82-87
-
-
Geschwind, M.D.1
Potter, C.A.2
Sattavat, M.3
-
20
-
-
0029741936
-
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease
-
Kretzschmar HA, Ironside JW, DeArmond SJ, Tateishi J: Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch Neurol 1996, 53: 913-920. 10.1001/archneur.1996.00550090125018
-
(1996)
Arch Neurol
, vol.53
, pp. 913-920
-
-
Kretzschmar, H.A.1
Ironside, J.W.2
DeArmond, S.J.3
Tateishi, J.4
-
21
-
-
0033045425
-
The efficiency of systematic sampling in stereology-reconsidered
-
Gundersen HJ, Jensen EB, Kieu K, Nielsen J: The efficiency of systematic sampling in stereology-reconsidered. J Microsc 1999, 193: 199-211. 10.1046/j.1365-2818.1999.00457.x
-
(1999)
J Microsc
, vol.193
, pp. 199-211
-
-
Gundersen, H.J.1
Jensen, E.B.2
Kieu, K.3
Nielsen, J.4
-
22
-
-
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. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
-
(1999)
Ann Neurol
, vol.46
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
-
23
-
-
33749254251
-
Classification of sporadic Creutzfeldt-Jakob disease revisited
-
Cali I, Castellani R, J Y, et al.: Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain 2006, 129: 2266-2277. 10.1093/brain/awl224
-
(2006)
Brain
, vol.129
, pp. 2266-2277
-
-
Cali, I.1
Castellani, R.J.Y.2
-
24
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
-
Kascsak RJ, Rubenstein R, Merz PA, et al.: Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol 1987, 61: 3688-3693.
-
(1987)
J Virol
, vol.61
, pp. 3688-3693
-
-
Kascsak, R.J.1
Rubenstein, R.2
Merz, P.A.3
-
25
-
-
77953027708
-
Sporadic corticobasal syndrome due to FTLD-TDP
-
Tartaglia MC, Sidhu M, V L, et al.: Sporadic corticobasal syndrome due to FTLD-TDP. Acta Neuropathol 2010, 119: 365-374. doi: 10.1007/s00401-009-0605-1 10.1007/s00401-009-0605-1
-
(2010)
Acta Neuropathol
, vol.119
, pp. 365-374
-
-
Tartaglia, M.C.1
Sidhu, M.V.L.2
-
26
-
-
84857612755
-
Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease
-
Kovacs GG, Molnar K, Keller E, Botond G, Budka H, Laszlo L: Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease. J Neuropathol Exp Neurol 2012, 71: 223-232. doi: 10.1097/NEN.0b013e318248aa70 10.1097/NEN.0b013e318248aa70
-
(2012)
J Neuropathol Exp Neurol
, vol.71
, pp. 223-232
-
-
Kovacs, G.G.1
Molnar, K.2
Keller, E.3
Botond, G.4
Budka, H.5
Laszlo, L.6
-
27
-
-
0028351904
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism
-
Monari L, Chen SG, P B, et al.: Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proc Natl Acad Sci USA 1994, 91: 2839-2842. 10.1073/pnas.91.7.2839
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 2839-2842
-
-
Monari, L.1
Chen, S.G.P.B.2
-
29
-
-
0032975733
-
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
-
Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H: A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Ann Neurol 1999, 45: 812-816. 10.1002/1531-8249(199906)45:6<812::AID-ANA20>3.0.CO;2-2
-
(1999)
Ann Neurol
, vol.45
, pp. 812-816
-
-
Hainfellner, J.A.1
Parchi, P.2
Kitamoto, T.3
Jarius, C.4
Gambetti, P.5
Budka, H.6
-
30
-
-
84874079703
-
Brain MRI in sporadic Jakob-Creutzfeldt disease is often misread
-
Geschwind MD, Kuryan C, Cattaruzza T, Vitali P, DeArmond S, Wong K: Brain MRI in sporadic Jakob-Creutzfeldt disease is often misread. Neurology 2010, 78: P03.018.
-
(2010)
Neurology
, vol.78
, pp. 18
-
-
Geschwind, M.D.1
Kuryan, C.2
Cattaruzza, T.3
Vitali, P.4
DeArmond, S.5
Wong, K.6
-
31
-
-
84862534521
-
The EEG in E200K familial CJD: relation to MRI patterns
-
Appel SA, Chapman J, Prohovnik I, Hoffman C, Cohen OS, Blatt I: The EEG in E200K familial CJD: relation to MRI patterns. J Neurol 2012, 259: 491-496. doi: 10.1007/s00415-011-6208-5 10.1007/s00415-011-6208-5
-
(2012)
J Neurol
, vol.259
, pp. 491-496
-
-
Appel, S.A.1
Chapman, J.2
Prohovnik, I.3
Hoffman, C.4
Cohen, O.S.5
Blatt, I.6
-
32
-
-
54249166290
-
MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study
-
Fulbright RK, Hoffmann C, Lee H, Pozamantir A, Chapman J, Prohovnik I: MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study. AJNR Am J Neuroradiol 2008, 29: 1638-1643. 10.3174/ajnr.A1217
-
(2008)
AJNR Am J Neuroradiol
, vol.29
, pp. 1638-1643
-
-
Fulbright, R.K.1
Hoffmann, C.2
Lee, H.3
Pozamantir, A.4
Chapman, J.5
Prohovnik, I.6
-
33
-
-
0026095028
-
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
-
Brown P, Goldfarb LG, Gibbs CJ Jr, Gajdusek DC: The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease. Eur J Epidemiol 1991, 7: 469-476. 10.1007/BF00143124
-
(1991)
Eur J Epidemiol
, vol.7
, pp. 469-476
-
-
Brown, P.1
Goldfarb, L.G.2
Gibbs, C.J.3
Gajdusek, D.C.4
-
34
-
-
0022973492
-
Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases
-
Brown P, Cathala F, Castaigne P, Gajdusek DC: Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986, 20: 597-602. 10.1002/ana.410200507
-
(1986)
Ann Neurol
, vol.20
, pp. 597-602
-
-
Brown, P.1
Cathala, F.2
Castaigne, P.3
Gajdusek, D.C.4
-
35
-
-
0038452462
-
Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease
-
Jarius C, Kovacs GG, Belay G, Hainfellner JA, Mitrova E, Budka H: Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease. Acta Neuropathol 2003, 105: 449-454. doi: 10.1007/s00401-002-0664-z
-
(2003)
Acta Neuropathol
, vol.105
, pp. 449-454
-
-
Jarius, C.1
Kovacs, G.G.2
Belay, G.3
Hainfellner, J.A.4
Mitrova, E.5
Budka, H.6
-
36
-
-
78651246462
-
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
-
Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P: Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis. Acta Neuropathol 2011, 121: 21-37. 10.1007/s00401-010-0760-4
-
(2011)
Acta Neuropathol
, vol.121
, pp. 21-37
-
-
Capellari, S.1
Strammiello, R.2
Saverioni, D.3
Kretzschmar, H.4
Parchi, P.5
-
37
-
-
0037065769
-
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease
-
Taratuto AL, Piccardo P, Reich EG: Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology 2002, 58: 362-367. 10.1212/WNL.58.3.362
-
(2002)
Neurology
, vol.58
, pp. 362-367
-
-
Taratuto, A.L.1
Piccardo, P.2
Reich, E.G.3
-
38
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
-
Medori R, Tritschler HJ, A LB, 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. doi: 10.1056/NEJM199202133260704 10.1056/NEJM199202133260704
-
(1992)
N Engl J Med
, vol.326
, pp. 444-449
-
-
Medori, R.1
Tritschler, H.J.2
-
39
-
-
0032976574
-
A subtype of sporadic prion disease mimicking fatal familial insomnia
-
Parchi P, Capellari S, S C, et al.: A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology 1999, 52: 1757-1763. 10.1212/WNL.52.9.1757
-
(1999)
Neurology
, vol.52
, pp. 1757-1763
-
-
Parchi, P.1
Capellari, S.S.C.2
-
40
-
-
84857029808
-
Hyperphosphorylated tau in young and middle-aged subjects
-
Elobeid A, Soininen H, Alafuzoff I: Hyperphosphorylated tau in young and middle-aged subjects. Acta Neuropathol 2012, 123: 97-104. doi: 10.1007/s00401-011-0906-z 10.1007/s00401-011-0906-z
-
(2012)
Acta Neuropathol
, vol.123
, pp. 97-104
-
-
Elobeid, A.1
Soininen, H.2
Alafuzoff, I.3
-
41
-
-
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, K D-u: 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
-
42
-
-
0020051603
-
Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway
-
Fraser H: Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway. Nature 1982, 295: 149-150. 10.1038/295149a0
-
(1982)
Nature
, vol.295
, pp. 149-150
-
-
Fraser, H.1
-
43
-
-
0026686855
-
Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis
-
Scott JR, Davies D, Fraser H: Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis. J Gen Virol 1992,73(Pt 7):1637-1644.
-
(1992)
J Gen Virol
, vol.73
, Issue.PART. 7
, pp. 1637-1644
-
-
Scott, J.R.1
Davies, D.2
Fraser, H.3
-
44
-
-
0031881510
-
Cerebral targeting indicates vagal spread of infection in hamsters fed with scrapie
-
Beekes M, McBride PA, Baldauf E: Cerebral targeting indicates vagal spread of infection in hamsters fed with scrapie. J Gen Virol 1998,79(Pt 3):601-607.
-
(1998)
J Gen Virol
, vol.79
, Issue.PART. 3
, pp. 601-607
-
-
Beekes, M.1
McBride, P.A.2
Baldauf, E.3
-
45
-
-
3843142665
-
The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system
-
Bouzamondo-Bernstein E, Hopkins SD, P S, et al.: The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system. J Neuropathol Exp Neurol 2004, 63: 882-899.
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 882-899
-
-
Bouzamondo, -B.E.1
Hopkins, S.D.P.S.2
-
46
-
-
84878325700
-
Intrinsic connectivity network disruption in progressive supranuclear palsy
-
Gardner RC, Boxer AL, A T, et al.: Intrinsic connectivity network disruption in progressive supranuclear palsy. Ann Neurol 2013. doi: 10.1002/ana.23844
-
(2013)
Ann Neurol
-
-
Gardner, R.C.1
Boxer, A.L.A.T.2
-
47
-
-
63649160214
-
Conformational diversity of wild-type Tau fibrils specified by templated conformation change
-
Frost B, Ollesch J, Wille H, Diamond MI: Conformational diversity of wild-type Tau fibrils specified by templated conformation change. J Biol Chem 2009, 284: 3546-3551.
-
(2009)
J Biol Chem
, vol.284
, pp. 3546-3551
-
-
Frost, B.1
Ollesch, J.2
Wille, H.3
Diamond, M.I.4
-
48
-
-
67649273927
-
Propagation of tau misfolding from the outside to the inside of a cell
-
Frost B, Jacks RL, Diamond MI: Propagation of tau misfolding from the outside to the inside of a cell. J Biol Chem 2009, 284: 12845-12852. 10.1074/jbc.M808759200
-
(2009)
J Biol Chem
, vol.284
, pp. 12845-12852
-
-
Frost, B.1
Jacks, R.L.2
Diamond, M.I.3
-
49
-
-
84861758226
-
Trans-cellular propagation of Tau aggregation by fibrillar species
-
Kfoury N, Holmes BB, Jiang H, Holtzman DM, Diamond MI: Trans-cellular propagation of Tau aggregation by fibrillar species. J Biol Chem 2012, 287: 19440-19451. doi: 10.1074/jbc.M112.346072 10.1074/jbc.M112.346072
-
(2012)
J Biol Chem
, vol.287
, pp. 19440-19451
-
-
Kfoury, N.1
Holmes, B.B.2
Jiang, H.3
Holtzman, D.M.4
Diamond, M.I.5
-
50
-
-
81755183039
-
Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease
-
Friedman-Levi Y, Meiner Z, Canello T, et al.: Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease. PLoS Pathog 2011, 7: e1002350. doi: 10.1371/journal.ppat.1002350 PPATHOGENS-D-11-01077 10.1371/journal.ppat.1002350
-
(2011)
PLoS Pathog
, vol.7
-
-
Friedman-Levi, Y.1
Meiner, Z.2
Canello, T.3
|