-
1
-
-
0026453980
-
Gerstmann-Sträussler syndrome - A variant type : Amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex
-
AMANO N., YAGISHITA S., YOKCI S., ITOH Y., KINOSHITA J., MIZUTANI T., MATSUISHI T, (1992), Gerstmann-Sträussler syndrome - A variant type : amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex. Acta Neumpathol. 84 : 15-23.
-
(1992)
Acta Neumpathol.
, vol.84
, pp. 15-23
-
-
Amano, N.1
Yagishita, S.2
Yokci, S.3
Itoh, Y.4
Kinoshita, J.5
Mizutani, T.6
Matsuishi, T.7
-
2
-
-
9544219691
-
Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)
-
BARBANTI P., FABBRINI G., SALVATORE M., PETRAROLI R., CARDONE F., MARAS B., EOUFSTRE M., MACCHI G., LENZI G.L, POCCHIARI M. (1996). Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation). Neurology 47: 734-740.
-
(1996)
Neurology
, vol.47
, pp. 734-740
-
-
Barbanti, P.1
Fabbrini, G.2
Salvatore, M.3
Petraroli, R.4
Cardone, F.5
Maras, B.6
Eoufstre, M.7
Macchi, G.8
Lenzi, G.L.9
Pocchiari, M.10
-
3
-
-
77951418320
-
Über eine eigenartige hereditȧr-familiäre Erkrankung des Zentralnervensystems
-
BRAUNMUHL A.V. (1954). Über eine eigenartige hereditȧr-familiäre Erkrankung des Zentralnervensystems. Arch. F. Psychiatr. U. Ztschr. Neurol. 191: 419-449.
-
(1954)
Arch. F. Psychiatr. U. Ztschr. Neurol.
, vol.191
, pp. 419-449
-
-
Braunmuhl, A.V.1
-
4
-
-
0026725538
-
The phenotypic expression of different mutations in transmissible human spongiform encephalopathy
-
BROWN P. (1992), The phenotypic expression of different mutations in transmissible human spongiform encephalopathy. Rev. Neurol. 148 : 317-327.
-
(1992)
Rev. Neurol.
, vol.148
, pp. 317-327
-
-
Brown, P.1
-
5
-
-
0027531316
-
β.P.P. participates in PrP amyloid plaques of Gerstmann-Sträussler-Scheirker disease, Indiana kindred
-
BUGIANI O., GIACCONE G., VERGA L., POLLO B., FRANGIONF B., FARLOW Mr, TAGLIAVINI F., GHETTI B. (1993). β.P.P. participates in PrP amyloid plaques of Gerstmann-Sträussler-Scheirker disease, Indiana kindred. J. Neuropath. Exp. Neurlo. 52 : 54-70.
-
(1993)
J. Neuropath. Exp. Neurlo.
, vol.52
, pp. 54-70
-
-
Bugiani, O.1
Giaccone, G.2
Verga, L.3
Pollo, B.4
Frangionf, B.5
Farlow, Mr.6
Tagliavini, F.7
Ghetti, B.8
-
6
-
-
0026650443
-
Inherited prion disease with 144 base pair gene insertion
-
COLLINGE J., BROWN J., HARDY J., MULLAN M., ROSSOR M.N., BAKER H., CROW T.J., LOFTHOUSE R., POULTER M., RIDLEY R., OWEN F., BENNETT C., DUNN G., HARDING A.E., QUINN N., DOSHI B., ROBERTS G.W., HONAVAR M., JANOTA I, LANTOS P.L. (1992). Inherited prion disease with 144 base pair gene insertion. Brain 115 : 687-710.
-
(1992)
Brain
, vol.115
, pp. 687-710
-
-
Collinge, J.1
Brown, J.2
Hardy, J.3
Mullan, M.4
Rossor, M.N.5
Baker, H.6
Crow, T.J.7
Lofthouse, R.8
Poulter, M.9
Ridley, R.10
Owen, F.11
Bennett, C.12
Dunn, G.13
Harding, A.E.14
Quinn, N.15
Doshi, B.16
Roberts, G.W.17
Honavar, M.18
Janota, I.19
Lantos, P.L.20
more..
-
7
-
-
0025330687
-
Prion dementia without charateristic pathology
-
COLLINGE J, OWEN F., POULTER M., LEACH M., CROW T.J., RussoR M.N., HARDY J., MULLAN M.J., JANOTA I., LANTOS P.L. (1990). Prion dementia without charateristic pathology. Lancet 336 : 7-9
-
(1990)
Lancet
, vol.336
, pp. 7-9
-
-
Collinge, J.1
Owen, F.2
Poulter, M.3
Leach, M.4
Crow, T.J.5
Russor, M.N.6
Hardy, J.7
Mullan, M.J.8
Janota, I.9
Lantos, P.L.10
-
8
-
-
0026849545
-
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene
-
DLOULY S.R., HSIAO K., FARLOW M.R., FOROUD T., CONNEALLY M.P., JOHNSON P., PRUSINER S.B., HODES M.E., GHETTI B. (1992). Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. Nature Genetics 1 : 64-67.
-
(1992)
Nature Genetics
, vol.1
, pp. 64-67
-
-
Dlouly, S.R.1
Hsiao, K.2
Farlow, M.R.3
Foroud, T.4
Conneally, M.P.5
Johnson, P.6
Prusiner, S.B.7
Hodes, M.E.8
Ghetti, B.9
-
9
-
-
0024473899
-
Pro → leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
-
DOH-URA K., TATEISHI J., SASAKI H., KIAMOTO T., SAKAKI Y., (1989). Pro → leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. Biochem and Biophys. Research Comm. 163 : 974-979.
-
(1989)
Biochem and Biophys. Research Comm.
, vol.163
, pp. 974-979
-
-
Doh-Ura, K.1
Tateishi, J.2
Sasaki, H.3
Kiamoto, T.4
Sakaki, Y.5
-
10
-
-
0029063658
-
New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome
-
FURUKAWA H., KITAMOTO T., TANAKA Y., TATEISHI J., (1995). New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome. Mol. Brain Research 30 : 385-388.
-
(1995)
Mol. Brain Research
, vol.30
, pp. 385-388
-
-
Furukawa, H.1
Kitamoto, T.2
Tanaka, Y.3
Tateishi, J.4
-
11
-
-
0000540668
-
Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems Zugleich ein Beitrag zur Frage des Vorzeitigen lokalen Alterns
-
GERSTMANN J., STRÄUSSLER E., SCHEINKER I. (1936). Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems Zugleich ein Beitrag zur Frage des Vorzeitigen lokalen Alterns. Z. Ges. Neurol. Psychiat. 154 : 748-762.
-
(1936)
Z. Ges. Neurol. Psychiat.
, vol.154
, pp. 748-762
-
-
Gerstmann, J.1
Sträussler, E.2
Scheinker, I.3
-
12
-
-
0001385519
-
Über ein noch nicht beschriebenes Reflexphä nomen bei ciner Erkrankung des zerebellären Systems
-
GFRSTMANN J. (1928). Über ein noch nicht beschriebenes Reflexphä nomen bei ciner Erkrankung des zerebellären Systems. Wien Medizin Wochenschr. 78 : 906-908.
-
(1928)
Wien Medizin Wochenschr.
, vol.78
, pp. 906-908
-
-
Gfrstmann, J.1
-
13
-
-
13344295093
-
Vascular variant of prion protein cerebral amyloidosis with (-positive neurofibrillary tangles : The phenotype of the stop codon 145 mutation in P.R.N.P.
-
GHETTI B., PICCARDO P., SPILLANTINI M.G., ICHIMIYAY., PORRO M., PERINI F., KITAMOTO T., TATEISHI J., SEILER C., FRANGIONE B., BUGIANI O., GIACCONE G., PRELLI F., GOEDERT M., DLOUHY S.R., TAGLIAVINI F. (1996a). Vascular variant of prion protein cerebral amyloidosis with (-positive neurofibrillary tangles : The phenotype of the stop codon 145 mutation in P.R.N.P. Proc. Natl. Acad. Sci. 93 : 744-748.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 744-748
-
-
Ghetti, B.1
Piccardo, P.2
Spillantini, M.G.3
Ichimiya, Y.4
Porro, M.5
Perini, F.6
Kitamoto, T.7
Tateishi, J.8
Seiler, C.9
Frangione, B.10
Bugiani, O.11
Giaccone, G.12
Prelli, F.13
Goedert, M.14
Dlouhy, S.R.15
Tagliavini, F.16
-
14
-
-
15844415943
-
Prion Protein Amyloidosis
-
GHETTI B., PICCARDO P. FRANGIONE B., BUGIANI O., GIACCONE G., YOUNG K., PRELLI F., FARLOW M.R., DLOUHY S.R., TAGLIAVINI F. (1996b) Prion Protein Amyloidosis. Brain Pathol. 6 : 127-145.
-
(1996)
Brain Pathol.
, vol.6
, pp. 127-145
-
-
Ghetti, B.1
Piccardo, P.2
Frangione, B.3
Bugiani, O.4
Giaccone, G.5
Young, K.6
Prelli, F.7
Farlow, M.R.8
Dlouhy, S.R.9
Tagliavini, F.10
-
15
-
-
0028375988
-
Familial Gerstmann-Sträussler-Scheinker Disease with Neurofibrillary Tangles
-
GHETTI B., TAGLIAVINI F., GIACCONE G., BUGIANI O., FRANGIONE B., FARLOW M,R., DLOUHY S.R. (1994). Familial Gerstmann-Sträussler-Scheinker Disease with Neurofibrillary Tangles. Mol. Neurobiol. 8 : 41-48.
-
(1994)
Mol. Neurobiol.
, vol.8
, pp. 41-48
-
-
Ghetti, B.1
Tagliavini, F.2
Giaccone, G.3
Bugiani, O.4
Frangione, B.5
Farlow, M.R.6
Dlouhy, S.R.7
-
16
-
-
0024856333
-
Gerstmann-Sträussler-Scheinker disease. II, Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family
-
GHEJTI B., TAGLIAVINI F., MASTERS C.L., BEYREUTHER K., GIACCONE G., VERGA L., FARLOW M.R., CONNEALLY P.M., DLOUHY S,R., AZZARELLI B., BUGIANI O. (1989). Gerstmann-Sträussler-Scheinker disease. II, Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family. Neurology 39 : 1453-1461.
-
(1989)
Neurology
, vol.39
, pp. 1453-1461
-
-
Ghejti, B.1
Tagliavini, F.2
Masters, C.L.3
Beyreuther, K.4
Giaccone, G.5
Verga, L.6
Farlow, M.R.7
Conneally, P.M.8
Dlouhy, S.R.9
Azzarelli, B.10
Bugiani, O.11
-
17
-
-
0028990981
-
The original Gerstmann-Sträussler-Scheinker family of austria : Divergent clinicopathological phenotypes but constant PrP genotype
-
HAINFELLNER J.A., BRANTNER-INTHALER S., CERVENAKOVA L., BROWN P., KITAMOTO T., TATEISHI J., DIRINGER H., LIBERSKI P.P., REGELE H., FEUCHT M., MAYR N., WESSELY P., SUMMER K., SEITELBERGER F., BUDKA H. (1995). The original Gerstmann-Sträussler-Scheinker family of austria : divergent clinicopathological phenotypes but constant PrP genotype. Brain Pathol. 5 : 201-211.
-
(1995)
Brain Pathol.
, vol.5
, pp. 201-211
-
-
Hainfellner, J.A.1
Brantner-Inthaler, S.2
Cervenakova, L.3
Brown, P.4
Kitamoto, T.5
Tateishi, J.6
Diringer, H.7
Liberski, P.P.8
Regele, H.9
Feucht, M.10
Mayr, N.11
Wessely, P.12
Summer, K.13
Seitelberger, F.14
Budka, H.15
-
18
-
-
0017683774
-
An autopsy case of Creutzfeldt-Jakob disease with Kuru-like neuropathological changes
-
HIRANO T., TSUCHIYAMA H., KAWAY K., MORI K. (1977). An autopsy case of Creutzfeldt-Jakob disease with Kuru-like neuropathological changes. Acta Path. Japonica 27 : 231-238.
-
(1977)
Acta Path. Japonica
, vol.27
, pp. 231-238
-
-
Hirano, T.1
Tsuchiyama, H.2
Kaway, K.3
Mori, K.4
-
19
-
-
0026849947
-
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
-
HSIAO K., DLOUHY S.R., FARLOW M.R., CASS C., DA COSTA M., CON NEARLY P.M., HODFS M.E., GHEITI B., PRUSINER S,B. (1992). Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. Nature Genetics 1 : 68-71.
-
(1992)
Nature Genetics
, vol.1
, pp. 68-71
-
-
Hsiao, K.1
Dlouhy, S.R.2
Farlow, M.R.3
Cass, C.4
Da Costa, M.5
Connearly, P.M.6
Hodfs, M.E.7
Gheiti, B.8
Prusiner, S.B.9
-
20
-
-
0025847141
-
A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome
-
HSIAO K., CASS C., SCHELLENBERG G.D., BIRD T., DEVINE-GAGF E., Wis NIEWSKI H., PRUSINER S.B. (1991). A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome. Neurology 41 : 681-684.
-
(1991)
Neurology
, vol.41
, pp. 681-684
-
-
Hsiao, K.1
Cass, C.2
Schellenberg, G.D.3
Bird, T.4
Devine-Gagf, E.5
Wisniewski, H.6
Prusiner, S.B.7
-
21
-
-
0025681138
-
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
-
HSUAO K.K., Scon M., FOSTER D., GROTH D.F., DE ARMOND S.I.. PRU SINER S.B. (1990). Spontaneous neurodegeneration in transgenic mice with mutant prion protein. Science 250 : 1587-1590.
-
(1990)
Science
, vol.250
, pp. 1587-1590
-
-
Hsuao, K.K.1
Scon, M.2
Foster, D.3
Groth, D.F.4
De Armond, S.I.5
Prusiner, S.B.6
-
22
-
-
0024519771
-
Linkage of a prion protein rnissense variant to Gerstmann-Sträussler syndrome
-
HSIAO K., BAKER H.F., CROW T.J., POULTFR M., OWEN F., TERWILLIGER J.D., WESTAWAY D., OTT J., PRUSINER S.B. (1989). Linkage of a prion protein rnissense variant to Gerstmann-Sträussler syndrome. Nature 338 : 342-345.
-
(1989)
Nature
, vol.338
, pp. 342-345
-
-
Hsiao, K.1
Baker, H.F.2
Crow, T.J.3
Poultfr, M.4
Owen, F.5
Terwilliger, J.D.6
Westaway, D.7
Ott, J.8
Prusiner, S.B.9
-
23
-
-
0000870682
-
Gerstmann-Sträussler-Scheinker disease showing (-Protein amyloid deposits in the peripheral regions of Prp-immunoreactive amylod plaques
-
IKEDA S., YANAGISAWA N., GLENNER G.G., ALLSOP D, (1992). Gerstmann-Sträussler-Scheinker disease showing (-Protein amyloid deposits in the peripheral regions of Prp-immunoreactive amylod plaques. Neurodegeneration 1 : 281-288.
-
(1992)
Neurodegeneration
, vol.1
, pp. 281-288
-
-
Ikeda, S.1
Yanagisawa, N.2
Glenner, G.G.3
Allsop, D.4
-
24
-
-
0028170720
-
A variant of Gerstmann-Sträussler-Scheinker disease cartying codon 105 mutation with codon 129 polymorphism of the prion protein gene : A clinicopathological study
-
ITOH Y., YAMADA M., HAYAKAWA M., SHOZAWA T., TANAKA J., MATSUSHITA M., KITAMOTO T., TATEISHI J., OTOMO E (1994). A variant of Gerstmann-Sträussler-Scheinker disease cartying codon 105 mutation with codon 129 polymorphism of the prion protein gene : A clinicopathological study. J. Neural. Sci. 127 : 77-86.
-
(1994)
J. Neural. Sci.
, vol.127
, pp. 77-86
-
-
Itoh, Y.1
Yamada, M.2
Hayakawa, M.3
Shozawa, T.4
Tanaka, J.5
Matsushita, M.6
Kitamoto, T.7
Tateishi, J.8
Otomo, E.9
-
25
-
-
0027185917
-
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gertsmann-Sträussler syndrome
-
KITAMOTO T., OHTA M., DOH-URA K., HITOSHI S., TERAO Y., TATEISHI J. (1993a). Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gertsmann-Sträussler syndrome. Biochem. Biophys. Res. Comm. 191 : 709-714.
-
(1993)
Biochem. Biophys. Res. Comm.
, vol.191
, pp. 709-714
-
-
Kitamoto, T.1
Ohta, M.2
Doh-Ura, K.3
Hitoshi, S.4
Terao, Y.5
Tateishi, J.6
-
26
-
-
0027497304
-
A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis
-
KITAMOTO T., AMANO N., TERAO Y., NAKAZATO Y., ISSHIKI T., MIZUTANI T., TATEISHI J. (1993b). A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis, Ann. Neural. 34 : 808-813.
-
(1993)
Ann. Neural.
, vol.34
, pp. 808-813
-
-
Kitamoto, T.1
Amano, N.2
Terao, Y.3
Nakazato, Y.4
Isshiki, T.5
Mizutani, T.6
Tateishi, J.7
-
27
-
-
0027236933
-
An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques
-
KITAMOTO T., LIZUKA R., TATEISHI J. (1993c). An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques. Biochem. Biophys. Res. Comm. 192 : 525-531.
-
(1993)
Biochem. Biophys. Res. Comm.
, vol.192
, pp. 525-531
-
-
Kitamoto, T.1
Lizuka, R.2
Tateishi, J.3
-
28
-
-
0025906297
-
Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker
-
KRETZSCHMAR H.A., HONOLD G., SETELBERHER F., FEUCHT M., WESSELY P., MEHHAEIN P., BUDKA H. (1991). Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker. Lancet. 337: 1160.
-
(1991)
Lancet
, vol.337
, pp. 1160
-
-
Kretzschmar, H.A.1
Honold, G.2
Setelberher, F.3
Feucht, M.4
Wessely, P.5
Mehhaein, P.6
Budka, H.7
-
29
-
-
0019778656
-
Creutzfeldt-Jakob disease virus isolations from the Gerstrnann-Sträusster syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephatopathies
-
MASTERS C.L., GAJUSEK C., GIBBS C. (1981). Creutzfeldt-Jakob disease virus isolations from the Gerstrnann-Sträusster syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephatopathies. Brain. 104 : 559-588.
-
(1981)
Brain
, vol.104
, pp. 559-588
-
-
Masters, C.L.1
Gajusek, C.2
Gibbs, C.3
-
30
-
-
0029398569
-
Prion disease (Pr P-A117V) presenting with ataxia instead of dementia
-
MASTRIANNI J.A., CURTIS M.T., OBERHOLIZER J.C., DA COSTA M.M., DeARMOND S., PRUSINER S.B., GABBERN J.Y. (1995). Prion disease (Pr P-A117V) presenting with ataxia instead of dementia. Neurology 45 : 2042-2050.
-
(1995)
Neurology
, vol.45
, pp. 2042-2050
-
-
Mastrianni, J.A.1
Curtis, M.T.2
Oberholizer, J.C.3
Da Costa, M.M.4
DeArmond, S.5
Prusiner, S.B.6
Gabbern, J.Y.7
-
31
-
-
0026559760
-
Colocalization of prion protein and protein in the same amyloid plaques in patients with Gerstmann-Sträussler Syndrome
-
MIYAZONO M., KITAMOTO T., IWAKI T., TATEISHI J. (1992). Colocalization of prion protein and (protein in the same amyloid plaques in patients with Gerstmann-Sträussler Syndrome. Acta Neuropathol. 83 : 333-339.
-
(1992)
Acta Neuropathol.
, vol.83
, pp. 333-339
-
-
Miyazono, M.1
Kitamoto, T.2
Iwaki, T.3
Tateishi, J.4
-
32
-
-
0024324177
-
Familial dementia with PrP-positive amyloid plaques : A variant of Gerstmann-Sträussler syndrome
-
NOCHLIN D., SUMI S.M., BIRD T.D., SNOW A.D., LEVENTUAL C.M., BEYREUTHER K., MASTERS C.L. (1989). Familial dementia with PrP-positive amyloid plaques : A variant of Gerstmann-Sträussler syndrome. Neurology 39 : 910-918.
-
(1989)
Neurology
, vol.39
, pp. 910-918
-
-
Nochlin, D.1
Sumi, S.M.2
Bird, T.D.3
Snow, A.D.4
Leventual, C.M.5
Beyreuther, K.6
Masters, C.L.7
-
33
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
PRUSINER S.B. (1982). Novel proteinaceous infectious particles cause scrapie. Science 216 : 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
34
-
-
0018943284
-
Experimental transmission of human subacute spongiform encephalopathy to small rodents. II. Ultrastructural study of spongy state in the gray and white matter
-
SATO Y., OHTA M., TATEISHI J. (1980). Experimental transmission of human subacute spongiform encephalopathy to small rodents. II. Ultrastructural study of spongy state in the gray and white matter. Acta Neuropath. 51 : 135-140.
-
(1980)
Acta Neuropath.
, vol.51
, pp. 135-140
-
-
Sato, Y.1
Ohta, M.2
Tateishi, J.3
-
35
-
-
0001441102
-
Eigenartige familiär-hereditäre Krankheit des Zentralnervensystems in einer niederösterreichischen Sippe
-
SEITELBERGER F. (1962). Eigenartige familiär-hereditäre Krankheit des Zentralnervensystems in einer niederösterreichischen Sippe. Wiener klinische Wochenschrift 41/42 : 687-691.
-
(1962)
Wiener Klinische Wochenschrift
, vol.41-42
, pp. 687-691
-
-
Seitelberger, F.1
-
36
-
-
0011888936
-
Assignment of the human and mouse prion protein gene to homologous chromosomes
-
SPARKES .S., SIMON M., COHN V.H., FOURNIER R.E.K., LEM J., KLISAK I., HEINZMANN C., BLATT C., LUCERO M., MOHANDAS T., DeARMAND S.J., WESTAWAY D., PRUSINER S.B., WENER L.P. (1986). Assignment of the human and mouse prion protein gene to homologous chromosomes, Proc. Natl. Sci. U.S.A. 83 : 7358-7362.
-
(1986)
Proc. Natl. Sci. U.S.A.
, vol.83
, pp. 7358-7362
-
-
Sparkes, S.1
Simon, M.2
Cohn, V.H.3
Fournier, R.E.K.4
Lem, J.5
Klisak, I.6
Heinzmann, C.7
Blatt, C.8
Lucero, M.9
Mohandas, T.10
DeArmand, S.J.11
Westaway, D.12
Prusiner, S.B.13
Wener, L.P.14
-
37
-
-
0028004290
-
Amyloid fibrils in Gerstmann-Straüssler-Scheinker disease (Indiana and Swedish Kindreds) express only PrP peptides encoded by the mutant allele
-
TAGLIAVINI F., PRELLI F., PORRO M., ROSSI G., GIACCONE G., FARLOW M.R., DLOUHY S.R., GHETTI B., BUGIANI O., FRANGIONE B. (1994), Amyloid fibrils in Gerstmann-Straüssler-Scheinker disease (Indiana and Swedish Kindreds) express only PrP peptides encoded by the mutant allele. Cell 79 : 695-703.
-
(1994)
Cell
, vol.79
, pp. 695-703
-
-
Tagliavini, F.1
Prelli, F.2
Porro, M.3
Rossi, G.4
Giaccone, G.5
Farlow, M.R.6
Dlouhy, S.R.7
Ghetti, B.8
Bugiani, O.9
Frangione, B.10
-
38
-
-
0027174804
-
A 68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred
-
TAGLIAVINI F., GIACCONE G., PRELLI F., VERGA L., PORRO M , TROJA NOWSKI J.Q., FARLOW M.R., FRANGIONE B., GHETTI B., BUGIANI O., (1993a). A 68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred. Brain Research 616 : 325-328.
-
(1993)
Brain Research
, vol.616
, pp. 325-328
-
-
Tagliavini, F.1
Giaccone, G.2
Prelli, F.3
Verga, L.4
Porro, M.5
Trojanowski, J.Q.6
Farlow, M.R.7
Frangione, B.8
Ghetti, B.9
Bugiani, O.10
-
39
-
-
0027367506
-
Synthetic peptides homologous to prion residues 106-147 form amyloïd-lide fibrils in vitro
-
TAGLIAVINI F., PRELLI F., VERGA L., GIACCONE G., SARMA R., GOREVIC P., GHETTI B., PASSERINI F., GHIBAUDI E., FORLONI G., SALMONA M., BUGIANI O., FRANGIONE B. (1993b). Synthetic peptides homologous to prion residues 106-147 form amyloïd-lide fibrils in vitro. Proc. Natl. Acad. Sci. 90 : 9678-9682.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 9678-9682
-
-
Tagliavini, F.1
Prelli, F.2
Verga, L.3
Giaccone, G.4
Sarma, R.5
Gorevic, P.6
Ghetti, B.7
Passerini, F.8
Ghibaudi, E.9
Forloni, G.10
Salmona, M.11
Bugiani, O.12
Frangione, B.13
-
40
-
-
0028878943
-
Inherited prion diseases and transmission to rodents
-
TATEISHI J., KITAMOTO T. (1995). Inherited prion diseases and transmission to rodents. Brain Pathol, 5 : 53-59.
-
(1995)
Brain Pathol
, vol.5
, pp. 53-59
-
-
Tateishi, J.1
Kitamoto, T.2
-
41
-
-
0025119522
-
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome
-
TATEISHI J., KITAMOTO T., DOH-URA K., SAKAKI Y., STEINMETZ G., TRANCHANT C., WARTER J.M., HELDT N. (1990). Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome. Neurology, 40 : 1578-1581.
-
(1990)
Neurology
, vol.40
, pp. 1578-1581
-
-
Tateishi, J.1
Kitamoto, T.2
Doh-Ura, K.3
Sakaki, Y.4
Steinmetz, G.5
Tranchant, C.6
Warter, J.M.7
Heldt, N.8
-
42
-
-
0019377039
-
Experimental transmission of human subacute spongiform encephalopathy to small rodents. III. Further transmission from three patients and distribution pattern of lesions in mice
-
TATEISHI J., DOI H., SATO Y., SUETOUGU M., ISSHII K., KUROIWA Y. (1981). Experimental transmission of human subacute spongiform encephalopathy to small rodents. III. Further transmission from three patients and distribution pattern of lesions in mice. Acta Neuropath, 53 : 161-163.
-
(1981)
Acta Neuropath
, vol.53
, pp. 161-163
-
-
Tateishi, J.1
Doi, H.2
Sato, Y.3
Suetougu, M.4
Isshii, K.5
Kuroiwa, Y.6
-
43
-
-
0018970884
-
Experimental transmission of human subacute spongiform encephalopathy to small rodents. Clinical and histological observations
-
TATEISHI J., SATO Y., KOGA M., DOI H., OHTA M. (1980). Experimental transmission of human subacute spongiform encephalopathy to small rodents. Clinical and histological observations. Acta Neuropath, 57 : 127-134.
-
(1980)
Acta Neuropath
, vol.57
, pp. 127-134
-
-
Tateishi, J.1
Sato, Y.2
Koga, M.3
Doi, H.4
Ohta, M.5
-
44
-
-
0026609502
-
Gerstmann-Sträussler-Scheinker disease in an Alsatian family : Clinical and genetic studies
-
TRANCHANT C., DOH-URA K., WARTER J.M., STEINMETZ G., CHEVALIER Y., HANAUER A., KITAMOTO T., TATEISHI J. (1992). Gerstmann-Sträussler-Scheinker disease in an Alsatian family : clinical and genetic studies, J. Neurol. Neurosurg. Psych., 55 : 185-187.
-
(1992)
J. Neurol. Neurosurg. Psych.
, vol.55
, pp. 185-187
-
-
Tranchant, C.1
Doh-Ura, K.2
Warter, J.M.3
Steinmetz, G.4
Chevalier, Y.5
Hanauer, A.6
Kitamoto, T.7
Tateishi, J.8
-
45
-
-
0025736005
-
Mutation du codon 117 du gène du prion dans une maladie de Gerstmann-Sträussler-Scheinker
-
TRANCHANT C., DOH-URA K., STEINWETZ G., CHEVALIER Y., KITAMOTO T., TATEISMI J., WARTER J.M., (1991). Mutation du codon 117 du gène du prion dans une maladie de Gerstmann-Sträussler-Scheinker Rev. Neurol. 147 : 274-278.
-
(1991)
Rev. Neurol.
, vol.147
, pp. 274-278
-
-
Tranchant, C.1
Doh-Ura, K.2
Steinwetz, G.3
Chevalier, Y.4
Kitamoto, T.5
Tateismi, J.6
Warter, J.M.7
-
46
-
-
0020072549
-
Démence pré-sénile familiale. Syndrome de Gerstmann-Sträussler-Scheinker
-
WARTER J.M., STEINMETZ G., HELDT N., RUMBACH L., MARESCAUX Ch., EBER A.M., COLLARD M., ROHMER F.. FLOQUET J., GUEDENET J.C., GEHIN P., WEBER M. (1982) Démence pré-sénile familiale. Syndrome de Gerstmann-Sträussler-Scheinker. Rev. Neurol. 138 : 107-121
-
(1982)
Rev. Neurol.
, vol.138
, pp. 107-121
-
-
Warter, J.M.1
Steinmetz, G.2
Heldt, N.3
Rumbach, L.4
Marescaux, Ch.5
Eber, A.M.6
Collard, M.7
Rohmer, F.8
Floquet, J.9
Guedenet, J.C.10
Gehin, P.11
Weber, M.12
-
47
-
-
0027729337
-
A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease
-
YAMADA M., ITOH Y., FUJIGASAKI H., NARUSE S., KANEKO K., KITAMOTO T., TATEISHI J., OTOMO E., HAYAKAWA M., TANAKA J., MATSUSHITA M., MIYATAKE T. (1993). A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease. Neurology, 43 : 2723-2724.
-
(1993)
Neurology
, vol.43
, pp. 2723-2724
-
-
Yamada, M.1
Itoh, Y.2
Fujigasaki, H.3
Naruse, S.4
Kaneko, K.5
Kitamoto, T.6
Tateishi, J.7
Otomo, E.8
Hayakawa, M.9
Tanaka, J.10
Matsushita, M.11
Miyatake, T.12
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