-
1
-
-
0022973492
-
Creutzfeldtjakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases
-
Brown P, Cathala F, Castaigne P, Gajdusek DC. CreutzfeldtJakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986; 20: 597-602.
-
(1986)
Ann Neurol
, vol.20
, pp. 597-602
-
-
Brown, P.1
Cathala, F.2
Castaigne, P.3
Gajdusek, D.C.4
-
2
-
-
0028235176
-
Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease
-
Brown P, Gibbs CI, Rodgers-Johnson P, Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 1994; 35: 513-29.
-
(1994)
Ann Neurol
, vol.35
, pp. 513-529
-
-
Brown, P.1
Gibbs, C.I.2
Rodgers-Johnson, P.3
-
3
-
-
0033926586
-
Creutzfeldt-jakob disease and the eye. I. Background and patient management
-
Leuck Q, McIlwaine GG, Zeidler M. Creutzfeldt-Jakob disease and the eye. I. Background and patient management. Eye 2000; 14: 263-90.
-
(2000)
Eye
, vol.14
, pp. 263-290
-
-
Leuck, Q.1
McIlwaine, G.G.2
Zeidler, M.3
-
4
-
-
0018574744
-
Creutzfeldt-jakob disease in france. Ii. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977
-
Brown P, Cathala F, Sadowsky D, Gajdusek DC. Creutzfeldt-Jakob disease in France. II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977. Ann Neurol 1979; 6: 430-7.
-
(1979)
Ann Neurol
, vol.6
, pp. 430-437
-
-
Brown, P.1
Cathala, F.2
Sadowsky, D.3
Gajdusek, D.C.4
-
5
-
-
12944258398
-
Creutzfeldt-jakob's disease: Clinicopathologic report of 15 cases and review of the literature (with special reference to a related disorder designated as subacute spongiform encephalopathy)
-
Siedler H, Malamud N. Creutzfeldt-Jakob's disease: clinicopathologic report of 15 cases and review of the literature (with special reference to a related disorder designated as subacute spongiform encephalopathy). J Neuropathol Exp Neurol 1983; 27: 381-402.
-
(1983)
J Neuropathol Exp Neurol
, vol.27
, pp. 381-402
-
-
Siedler, H.1
Malamud, N.2
-
6
-
-
0021054130
-
Creutzfeldt-jakob disease in japan
-
Tsuji S, Kuroiwa Y. Creutzfeldt-Jakob disease in Japan. Neurology 1983; 33: 1503-6.
-
(1983)
Neurology
, vol.33
, pp. 1503-1506
-
-
Tsuji, S.1
Kuroiwa, Y.2
-
8
-
-
0021333827
-
A retrospective study of creutzfeldt-jakob disease in england and wales 1970-79. I. Clinical features
-
Will RG, Matthews WB. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I. Clinical features. J Neurol Neurosurg Psychiatry 1984; 47: 134-40.
-
(1984)
J Neurol Neurosurg Psychiatry
, vol.47
, pp. 134-140
-
-
Will, R.G.1
Matthews, W.B.2
-
9
-
-
0026581952
-
Phenotypic characteristics of familial creutzfeldt-jakob disease associated with the codon 178asn prnp mutation
-
Brown P, Goldfarb LG, Kovanen J, Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation. Ann Neurol 1992; 31: 282-5.
-
(1992)
Ann Neurol
, vol.31
, pp. 282-285
-
-
Brown, P.1
Goldfarb, L.G.2
Kovanen, J.3
-
11
-
-
0002409051
-
Human spongiform encephalopathy
-
Baker HF, Ridley RM, editors, Totowa, NJ: Humana Press
-
De Silva R. Human spongiform encephalopathy. In: Baker HF, Ridley RM, editors. Methods in molecular medicine: prion diseases. Totowa, NJ: Humana Press, 1996: 15-33.
-
(1996)
Methods in Molecular Medicine: Prion Diseases
, pp. 15-33
-
-
De Silva, R.1
-
13
-
-
84964191906
-
On some aspects of cerebral degeneration in later life
-
Nevin S. On some aspects of cerebral degeneration in later life. Proc R Soc Lond B 1967; 60: 517-26.
-
(1967)
Proc R Soc Lond B
, vol.60
, pp. 517-526
-
-
Nevin, S.1
-
14
-
-
0015549846
-
The clinical characteristics of transmissible creutzfeldt-jakob disease
-
Roos R, Gajdusek DC, Gibbs Q. The clinical characteristics of transmissible Creutzfeldt-Jakob disease. Brain 1973; 96: 1-20.
-
(1973)
Brain
, vol.96
, pp. 1-20
-
-
Roos, R.1
Gajdusek, D.C.2
Gibbs, Q.3
-
15
-
-
0018294272
-
La maladie de creutzfeldt-jakob en france continentale: Etude retrospective de 1968 11 1977
-
Cathala F, Brown P, Castaigne P, Gajdusek DC. La maladie de Creutzfeldt-Jakob en France continentale: etude retrospective de 1968 11 1977. Rev Neurol (Paris) 1979; 135: 439-54.
-
(1979)
Rev Neurol
, vol.135
, pp. 439-454
-
-
Cathala, F.1
Brown, P.2
Castaigne, P.3
Gajdusek, D.C.4
-
16
-
-
0024207490
-
A retrospective study of creutzfeldt-jakob disease in italy (1972-1986)
-
Masullo C, Pocchiari M, Neri G, A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986). Eur J Epidemiol 1988; 4: 482-7.
-
(1988)
Eur J Epidemiol
, vol.4
, pp. 482-487
-
-
Masullo, C.1
Pocchiari, M.2
Neri, G.3
-
17
-
-
0032585594
-
Gibbs q. Creutzfeldt-jakob disease and related transmissible spongiform encephalopathies
-
Johnston RT, Gibbs q. 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
-
-
Johnston, R.T.1
-
18
-
-
0026667331
-
Friendly fire' in medicine: Hormones, homografts, and creutzfeldt-jakob disease
-
Brown P, Preece MA, Will RG. 'Friendly fire' in medicine: hormones, homografts, and Creutzfeldt-Jakob disease. Lancet 1992; 340: 24-7.
-
(1992)
Lancet
, vol.340
, pp. 24-27
-
-
Brown, P.1
Preece, M.A.2
Will, R.G.3
-
19
-
-
0001699149
-
Creutzfeldt-jakob disease from contaminated growth hormone extracts in france
-
Billette De Villemeur T, Deslys J-P, Pradel A, Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France. Neurology 1996; 47: 690-5.
-
(1996)
Neurology
, vol.47
, pp. 690-695
-
-
Billette De Villemeur, T.1
Deslys, J.-P.2
Pradel, A.3
-
20
-
-
0032497692
-
Creutzfeldt-jakob disease via dural and corneal transplants
-
Lang QG, Heckmann JG, Neundorfer B. Creutzfeldt-Jakob disease via dural and corneal transplants. J Neural Sci 1998; 160: 128-39.
-
(1998)
J Neural Sci
, vol.160
, pp. 128-139
-
-
Lang, Q.G.1
Heckmann, J.G.2
Neundorfer, B.3
-
21
-
-
0016140052
-
Transmission of creutzfeldt-jakob disease from man to squirrel monkey
-
Zlotnik I, Grant DP, Dayan AD, Earl Q. Transmission of Creutzfeldt-Jakob disease from man to squirrel monkey. Lancet 1974; 11: 435-8.
-
(1974)
Lancet
, vol.11
, pp. 435-438
-
-
Zlotnik, I.1
Grant, D.P.2
Dayan, A.D.3
Earl, Q.4
-
22
-
-
0002442331
-
Klinische und anatomische untersuchungen tiber eine eigenartige organische erkrankung des zentralnervensystems in praesenium
-
Heidenhain A. Klinische und anatomische Untersuchungen tiber eine eigenartige organische Erkrankung des Zentralnervensystems in Praesenium. Z Ges Neurol Psych 1928; 118: 49-114.
-
(1928)
Z Ges Neurol Psych
, vol.118
, pp. 49-114
-
-
Heidenhain, A.1
-
23
-
-
78651037345
-
A rare presenile dementia associated with cortical blindness (Heidenhain's syndrome)
-
Meyer A, Leigh D, Bagg CE. A rare presenile dementia associated with cortical blindness (Heidenhain's syndrome). J Neurol Neurosurg Psychiatry 1954; 17: 129-33.
-
(1954)
J Neurol Neurosurg Psychiatry
, vol.17
, pp. 129-133
-
-
Meyer, A.1
Leigh, D.2
Bagg, C.E.3
-
24
-
-
0342636055
-
Cortico-striatal degeneration of the creutzfeldt-jakob type
-
Silberman J, Cravioto H, Feigin I. Cortico-striatal degeneration of the Creutzfeldt-Jakob type. Neuropathol Exp Neurol 1961; 20: 105-18.
-
(1961)
Neuropathol Exp Neurol
, vol.20
, pp. 105-118
-
-
Silberman, J.1
Cravioto, H.2
Feigin, I.3
-
25
-
-
0343070400
-
Clinical observations on seven pathologically proved cases of creutzfeldt-jakob disease
-
Butler HM, Williams GH, McCormack LJ. Clinical observations on seven pathologically proved cases of Creutzfeldt-Jakob disease. Trans Am Neurol Assoc 1963; 88: 30-2.
-
(1963)
Trans am Neurol Assoc
, vol.88
, pp. 30-32
-
-
Butler, H.M.1
Williams, G.H.2
McCormack, L.J.3
-
26
-
-
0343942093
-
Gauthier e. Sur la maladie de creutzfeld-jakob: Deux observations anatomo-cliniques. Conception uniciste
-
Amyot R, Gauthier e. Sur la maladie de Creutzfeld-Jakob: deux observations anatomo-cliniques. Conception uniciste. Rev Neurol (Paris) 1964; 110: 473-88.
-
(1964)
Rev Neurol
, vol.110
, pp. 473-488
-
-
Amyot, R.1
-
27
-
-
0014356772
-
Encephalopathie presenile d'evolution subaigue type heidenhain
-
Boudouresques J, Toga M, Roger J, Encephalopathie presenile d'evolution subaigue type Heidenhain. Rev Neurol (Paris) 1968; 119: 468-76.
-
(1968)
Rev Neurol
, vol.119
, pp. 468-476
-
-
Boudouresques, J.1
Toga, M.2
Roger, J.3
-
28
-
-
0014910449
-
Subakute prasenile spongiforme encephalopathie mit occipitalem schwerpunkt und rindenblindheit
-
Schlote W. Subakute prasenile spongiforme Encephalopathie mit occipitalem Schwerpunkt und Rindenblindheit (Heidenhain-Syndrom). Arch Psych Nervenk 1970; 2l3: 345-69.
-
(1970)
Arch Psych Nervenk
, vol.213
, pp. 345-369
-
-
Schlote, W.1
-
29
-
-
0015967377
-
Typ heidenhain' der subakuten spongiosen encephalopathie (Sse) creutzfeldt-jakob
-
Hopf HC, Althaus HH, Sabuneu S. Typ Heidenhain' der subakuten spongiosen Encephalopathie (SSE) Creutzfeldt-Jakob. Z Neurol 1974; 206: 149-56.
-
(1974)
Z Neurol
, vol.206
, pp. 149-156
-
-
Hopf, H.C.1
Althaus, H.H.2
Sabuneu, S.3
-
30
-
-
0016475470
-
Subakute spongiose encephalopathie vom typ heidenhain
-
Bosch PL, Vass K. Subakute spongiose Encephalopathie vom typ Heidenhain. Nervenarzt 1975; 46: 160-2.
-
(1975)
Nervenarzt
, vol.46
, pp. 160-162
-
-
Bosch, P.L.1
Vass, K.2
-
31
-
-
0017473995
-
Przypadek choroby jakobacreutzfeldta 0 rzadko spotykanej topografii zmian (Tzw. Zespolu heidenhaina)
-
Iwanowski L, Kunicka J. Przypadek choroby JakobaCreutzfeldta 0 rzadko spotykanej topografii zmian (tzw. zespolu Heidenhaina). Neurologiai Neurochirurgia Polska 1977; 11: 247-50.
-
(1977)
Neurologiai Neurochirurgia Polska
, vol.11
, pp. 247-250
-
-
Iwanowski, L.1
Kunicka, J.2
-
32
-
-
0020472679
-
Zur klinik, neuropathologie und pathogenese der creutzfeldt-jakobschen krankheit anhand von 40 gesicherten fallen
-
Galvez S, Dorr-Zegers O, Cartier I. Zur Klinik, Neuropathologie und Pathogenese der Creutzfeldt-Jakobschen Krankheit anhand von 40 gesicherten Fallen. Nervenarzt 1982; 53: l32-40.
-
(1982)
Nervenarzt
, vol.53
, pp. l32-l40
-
-
Galvez, S.1
Dorr-Zegers, O.2
Cartier, I.3
-
33
-
-
0020785748
-
Forma corticocerebellare della malattia di creutzfeldt-jakob: Studio anotomo-clinico
-
Piccardo A, Tabaton M, Meneghini S, Leonardi A. Forma corticocerebellare della malattia di Creutzfeldt-Jakob: studio anotomo-clinico. Pathologica 1983; 75: 577-81.
-
(1983)
Pathologica
, vol.75
, pp. 577-581
-
-
Piccardo, A.1
Tabaton, M.2
Meneghini, S.3
Leonardi, A.4
-
34
-
-
0028182479
-
Utility of 123i_imp spect brain scans for the early detection of site-specific abnormalities in creutzfeldt-jakob disease (Heidenhain type): A case study
-
Jibiki I, Fukushima T, Kobayashi K, Utility of 123I_IMP SPECT brain scans for the early detection of site-specific abnormalities in Creutzfeldt-Jakob disease (Heidenhain type): a case study. Neuropsychobiology 1994; 29: 117-9.
-
(1994)
Neuropsychobiology
, vol.29
, pp. 117-119
-
-
Jibiki, I.1
Fukushima, T.2
Kobayashi, K.3
-
35
-
-
0020598020
-
Creutzfeldt-jakob disease: A case with extensive white matter degeneration and optic atrophy
-
Kitagawa Y, Gotoh F, Koto A, Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy. J Neurol 1983; 229: 97-101.
-
(1983)
J Neurol
, vol.229
, pp. 97-101
-
-
Kitagawa, Y.1
Gotoh, F.2
Koto, A.3
-
36
-
-
0025924232
-
Encefalopatia espongiforme y degneracion multisistemica
-
Ferrer I, Saracibar N, Gonzalez G. Encefalopatia espongiforme y degneracion multisistemica. Neurologia 1991; 6: 29-33.
-
(1991)
Neurologia
, vol.6
, pp. 29-33
-
-
Ferrer, I.1
Saracibar, N.2
Gonzalez, G.3
-
37
-
-
0025870979
-
Serial mr imaging in creutzfeldt-jakob disease
-
Uchino A, Yoshinaga M, Shiokawa O, Hata H, Ohno M Serial MR imaging in Creutzfeldt-Jakob disease. Neuroradiology 1991; 33: 364-7.
-
(1991)
Neuroradiology
, vol.33
, pp. 364-367
-
-
Uchino, A.1
Yoshinaga, M.2
Shiokawa, O.3
Hata, H.4
Ohno, M.5
-
39
-
-
0026580453
-
Serial computed tomographic and electroencephalographic studies in creutzfeldt-jakob disease
-
Hayashi R, Hanyu N, Kuwabara T, Moriyama S. Serial computed tomographic and electroencephalographic studies in Creutzfeldt-Jakob disease. Acta Neurol Scand 1992; 85: 161-5.
-
(1992)
Acta Neurol Scand
, vol.85
, pp. 161-165
-
-
Hayashi, R.1
Hanyu, N.2
Kuwabara, T.3
Moriyama, S.4
-
40
-
-
0026913646
-
Case of panencephalopathic type of creutzfeldt-jakob disease with retinal involvement. Hokkaido igaku zasshi-hokkaido
-
Sato Y, Chiba S, Miyagishi T. A case of panencephalopathic type of Creutzfeldt-Jakob disease with retinal involvement. Hokkaido Igaku Zasshi-Hokkaido. J Med Sci 1992; 67: 703-11.
-
(1992)
J Med Sci
, vol.67
, pp. 703-711
-
-
Sato, Y.1
Chiba, S.2
Miyagishi, T.A.3
-
41
-
-
0026742613
-
Demonstration of the transmissible agent in tissue from a pregnant woman with creutzfeldt-jakob disease
-
Tarnai Y, Kojima H, Kitajima R, Demonstration of the transmissible agent in tissue from a pregnant woman with Creutzfeldt-Jakob disease. N Engl J Med 1992; 327: 649.
-
(1992)
N Engl J Med
, vol.327
, pp. 649
-
-
Tarnai, Y.1
Kojima, H.2
Kitajima, R.3
-
42
-
-
0027378249
-
A new point mutation of the prion protein gene in creutzfeldt-jakob disease
-
Pocchiari M, Salvatore M, Cutruzzola F, A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease. Ann Neurol 1993; 34: 802-7.
-
(1993)
Ann Neurol
, vol.34
, pp. 802-807
-
-
Pocchiari, M.1
Salvatore, M.2
Cutruzzola, F.3
-
43
-
-
0027395652
-
Transmission of creutzfeldt-jakob disease by handling of dura mater
-
Weber T, Tumani H, Holdorff B, Transmission of Creutzfeldt-Jakob disease by handling of dura mater. Lancet 1993; 341: 123-4.
-
(1993)
Lancet
, vol.341
, pp. 123-124
-
-
Weber, T.1
Tumani, H.2
Holdorff, B.3
-
44
-
-
0028143763
-
Magnetic resonance imaging and neuropathological findings in two patients with creutzfeldt-jakob disease
-
Iwasaki Y, Ikeda K, Tagaya N, Kinoshita M. Magnetic resonance imaging and neuropathological findings in two patients with Creutzfeldt-Jakob disease. J Neurol Sci 1994; 126: 228-31.
-
(1994)
J Neurol Sci
, vol.126
, pp. 228-231
-
-
Iwasaki, Y.1
Ikeda, K.2
Tagaya, N.3
Kinoshita, M.4
-
45
-
-
0028111012
-
Creutzfeldt-jakob disease with a point mutation at codon 232 of prion protein: A case report
-
Shimizu T, Tanaka K, Tanahashi N, Fukuuchi Y, Kitamoto T. Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein: a case report. Rinsho Shinkeigaku-Clin Neurol 1994; 24: 590-2.
-
(1994)
Rinsho Shinkeigaku-Clin Neurol
, vol.24
, pp. 590-592
-
-
Shimizu, T.1
Tanaka, K.2
Tanahashi, N.3
Fukuuchi, Y.4
Kitamoto, T.5
-
47
-
-
0031796888
-
Single-photon emission computed tomography image of benzodiazepine receptors in a patient with creutzfeldt-jakob disease
-
Itoh Y, Amano T, Shimizu T, Hashimoto J, Kubo A, Fukuuchi Y. Single-photon emission computed tomography image of benzodiazepine receptors in a patient with Creutzfeldt-Jakob disease. Intern Med 1998; 37: 896-900.
-
(1998)
Intern Med
, vol.37
, pp. 896-900
-
-
Itoh, Y.1
Amano, T.2
Shimizu, T.3
Hashimoto, J.4
Kubo, A.5
Fukuuchi, Y.6
-
48
-
-
0032584789
-
Creutzfeldt-jakob-krankheit bei einem duratransplantat-empfanger
-
Radbauer C, Hainfellner JA, Gaudernak T, Deecke L, Budka H. Creutzfeldt-Jakob-Krankheit bei einem DuraTransplantat-Empfanger: Erstbeobachtung in Osterreich. Wien Klin Wochenschr 1998; 110: 496-500.
-
(1998)
Erstbeobachtung in Osterreich. Wien Klin Wochenschr
, vol.110
, pp. 496-500
-
-
Radbauer, C.1
Hainfellner, J.A.2
Gaudernak, T.3
Deecke, L.4
Budka, H.5
-
49
-
-
28144454276
-
Wen me. Creutzfeldt-jakob disease: Clinical analysis of eight cases
-
Hsieh MJ, Wang PY, Chia LG, Kao CH, Wen Me. Creutzfeldt-Jakob disease: clinical analysis of eight cases. Chung Hua i Hsueh Tsa Chih-Chinese Med J 1996; 57: 284-8.
-
(1996)
Chung Hua I Hsueh Tsa Chih-Chinese Med J
, vol.57
, pp. 284-288
-
-
Hsieh, M.J.1
Wang, P.Y.2
Chia, L.G.3
Kao, C.H.4
-
50
-
-
0032251653
-
Creutzfeldt-jakob disease in sweden
-
Lundberg PO. Creutzfeldt-Jakob disease in Sweden. J Neurol Neurosurg Psychiatry 1998; 65: 836-41.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, pp. 836-841
-
-
Lundberg, P.O.1
-
51
-
-
0015352030
-
Argentophilic plaques in creutzfeldt-jakob disease
-
Hirano A, Ghatak NR, Johnson AB, Partnow MJ, Gomori AJ. Argentophilic plaques in Creutzfeldt-Jakob disease. Arch Neurol 1972; 26: 530-42.
-
(1972)
Arch Neurol
, vol.26
, pp. 530-542
-
-
Hirano, A.1
Ghatak, N.R.2
Johnson, A.B.3
Partnow, M.J.4
Gomori, A.J.5
-
52
-
-
0344352503
-
Creutzfeldt-jakob disease in a husband and wife
-
Brown P, Cervenakova L, McShane L, Creutzfeldt-Jakob disease in a husband and wife. Neurology 1998; 50: 684-8.
-
(1998)
Neurology
, vol.50
, pp. 684-688
-
-
Brown, P.1
Cervenakova, L.2
McShane, L.3
-
53
-
-
0017194326
-
Electroencephalographic and clinicopathological studies on creutzfeldt-jakob syndrome
-
Goto K, Umezaki H, Suetsugu M. Electroencephalographic and clinicopathological studies on Creutzfeldt-Jakob syndrome. J Neurol Neurosurg Psychiatry 1976; 39: 931-40.
-
(1976)
J Neurol Neurosurg Psychiatry
, vol.39
, pp. 931-940
-
-
Goto1
Umezaki, K.H.2
Suetsugu, M.3
-
54
-
-
0024416770
-
An autopsy case of panencephalopathic type of creutzfeldt-jakob disease: An early clinical sign documented by magnetic resonance imaging
-
Okiyama R, Tsuchiya K, Furukawa T, Tsukagoshi H, Kosaka K. An autopsy case of panencephalopathic type of Creutzfeldt-Jakob disease: an early clinical sign documented by magnetic resonance imaging. Rinsho Shinkeigaku-Clin Neurol 1989; 29: 1048-51.
-
(1989)
Rinsho Shinkeigaku-Clin Neurol
, vol.29
, pp. 1048-1051
-
-
Okiyama, R.1
Tsuchiya, K.2
Furukawa, T.3
Tsukagoshi, H.4
Kosaka, K.5
-
55
-
-
0024894291
-
Creutzfeldt-jakob disease: Report of 10 neuropathologicallyverified cases in argentina
-
Taratuto AL, Piccardo P, Leiguarda R, Creutzfeldt-Jakob disease: report of 10 neuropathologicallyverified cases in Argentina. Medicina (Buenos Aires) 1989; 49: 293-303.
-
(1989)
Medicina
, vol.49
, pp. 293-303
-
-
Taratuto, A.L.1
Piccardo, P.2
Leiguarda, R.3
-
57
-
-
0020973777
-
Gerstmann-straussler-scheinker disease with coincidental familial onset
-
Hudson AJ, Farrell MA, Kalnins R, Kaufmann JCE. Gerstmann-Straussler-Scheinker disease with coincidental familial onset. Ann Neurol 1983; 14: 670-8.
-
(1983)
Ann Neurol
, vol.14
, pp. 670-678
-
-
Hudson, A.J.1
Farrell, M.A.2
Kalnins, R.3
Kaufmann, J.C.E.4
-
58
-
-
0019136804
-
Gerstrnann-straussler-scheinker's disease. Electronmicroscopic observations on a brain biopsy
-
Schlote W, Boellaard JW, Schumm F, Stohr M. Gerstrnann-Straussler-Scheinker's disease. Electronmicroscopic observations on a brain biopsy. Acta Neuropathol 1980; 52: 203-11.
-
(1980)
Acta Neuropathol
, vol.52
, pp. 203-211
-
-
Schlote, W.1
Boellaard, J.W.2
Schumm, F.3
Stohr, M.4
-
59
-
-
0343942507
-
The human diffusely projecting system: Evoked potentials and interactions
-
Nelson JR, Leffman H. The human diffusely projecting system: evoked potentials and interactions. Arch Neurol 1963; 8: 544-56.
-
(1963)
Arch Neurol
, vol.8
, pp. 544-556
-
-
Nelson, J.R.1
Leffman, H.2
-
60
-
-
0000612171
-
Subacute spongiform encephalopathy: A subacute form of encephalopathy attributable to vascular dysfunction
-
Nevin S, McMenemey WH, Behrman S, Jones DP. Subacute spongiform encephalopathy: a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy). Brain 1960; 83: 519.
-
(1960)
Brain
, vol.83
, pp. 519
-
-
Nevin, S.1
McMenemey, W.H.2
Behrman, S.3
Jones, D.P.4
-
61
-
-
0016541521
-
Encephalopathie spongiforme subaigue et maladie de creutzfeldt-jakob: A propos d'un cas
-
Morice J, Turpin JC, Pluot M, Level G. Encephalopathie spongiforme subaigue et maladie de Creutzfeldt-Jakob: a propos d'un cas. Rev Neurol (Paris) 1975; 131: 573-82.
-
(1975)
Rev Neurol
, vol.131
, pp. 573-582
-
-
Morice, J.1
Turpin, J.C.2
Pluot, M.3
Level, G.4
-
62
-
-
0018398253
-
Creutzfeldt-jakob disease in france. I. Retrospective study of the paris area during the ten-year period 1968-1977
-
Brown P, Cathala F. Creutzfeldt-Jakob disease in France. I. Retrospective study of the Paris area during the ten-year period 1968-1977. Ann Neurol 1979; 5: 189-92.
-
(1979)
Ann Neurol
, vol.5
, pp. 189-192
-
-
Brown, P.1
Cathala, F.2
-
63
-
-
0026606037
-
Creutzfeldt-jakob disease: Focal symmetrical cortical involvement demonstrated by mr imaging
-
Falcone S, Quencer RM, Bowen B, Bruce JH, Naidich TP. Creutzfeldt-Jakob disease: focal symmetrical cortical involvement demonstrated by MR imaging. Am J Neuroradiol 1992; l3: 403-6.
-
(1992)
Am J Neuroradiol
, vol.13
, pp. 403-406
-
-
Falcone, S.1
Quencer, R.M.2
Bowen, B.3
Bruce, J.H.4
Naidich, T.P.5
-
64
-
-
0030011664
-
Mr imaging of creutzfeldt-jakob disease
-
Finkenstaedt M, Szudra A, Zerr I, MR imaging of Creutzfeldt-Jakob disease. Radiology 1996; 199: 793-8.
-
(1996)
Radiology
, vol.199
, pp. 793-798
-
-
Finkenstaedt, M.1
Szudra, A.2
Zerr, I.3
-
65
-
-
0031808093
-
An autopsied case of creutzfeldt-jakob disease with the lateral geniculate body lesion showing antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses
-
Aoki T, Kobayashi K, Jibiki I, An autopsied case of Creutzfeldt-Jakob disease with the lateral geniculate body lesion showing antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses. Psychiatry Clin Neurosci 1998; 52: 333-7.
-
(1998)
Psychiatry Clin Neurosci
, vol.52
, pp. 333-337
-
-
Aoki, T.1
Kobayashi, K.2
Jibiki, I.3
-
66
-
-
0024377357
-
Palinopsia as a presenting manifestation of creutzfeldt-jakob disease
-
Purvin V, Bonnin J, Goodman J. Palinopsia as a presenting manifestation of Creutzfeldt-Jakob disease. J Clin Neuroophthalmol 1989; 9: 242-6.
-
(1989)
J Clin Neuroophthalmol
, vol.9
, pp. 242-246
-
-
Purvin, V.1
Bonnin, J.2
Goodman, J.3
-
67
-
-
0027296031
-
Abnormal eye movements in creutzfeldt-jakob disease
-
Grant MP, Cohen M, Petersen RB, Abnormal eye movements in Creutzfeldt-Jakob disease. Ann Neurol 1993; 34: 192-7.
-
(1993)
Ann Neurol
, vol.34
, pp. 192-197
-
-
Grant, M.P.1
Cohen, M.2
Petersen, R.B.3
-
68
-
-
0028941867
-
Homonymous field defect as the first manifestation of creutzfeldt-jakob disease
-
Vargas ME, Kupersmith MJ, Savino PJ, Petito F, Frohman LP, Warren FA. Homonymous field defect as the first manifestation of Creutzfeldt-Jakob disease. Am J Ophthalmol 1995; 119: 497-504.
-
(1995)
Am J Ophthalmol
, vol.119
, pp. 497-504
-
-
Vargas, M.E.1
Kupersmith, M.J.2
Savino, P.J.3
Petito, F.4
Frohman, L.P.5
Warren, F.A.6
-
69
-
-
0031438679
-
Sehverschlechterung als erstymptom einer creutzfeld-jakob-erkrankung
-
Rauber M, Knaflic D, Mester U. Sehverschlechterung als Erstymptom einer Creutzfeld-Jakob-Erkrankung. Klin Monatsbl Augenheilkd 1997; 211: A10-A13.
-
(1997)
Klin Monatsbl Augenheilkd
, vol.211
-
-
Rauber, M.1
Knaflic, D.2
Mester, U.3
-
71
-
-
0006581453
-
The clinical picture in creutzfeldt-jakob disease
-
Fisher CM. The clinical picture in Creutzfeldt-Jakob disease. Trans Am Neurol Assoc 1960; 85: 147-50.
-
(1960)
Trans am Neurol Assoc
, vol.85
, pp. 147-150
-
-
Fisher, C.M.1
-
72
-
-
0019199110
-
Richardson ep. Case records of the massachusetts general hospital. Case 45-1980
-
Wolpow ER, Richardson EP. Case records of the Massachusetts General Hospital. Case 45-1980. N Engl J Med 1980; 303: 1162-71.
-
(1980)
N Engl J Med
, vol.303
, pp. 1162-1171
-
-
Wolpow, E.R.1
-
73
-
-
0023619212
-
Iodine-123 hipdm brain imaging findings in subacute spongiform encephalopathy (Creutzfeldt-jakob disease)
-
Shih WI, Markesbery WR, Clark DB, Iodine-123 HIPDM brain imaging findings in subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). J Nucl Med 1987; 28: 1484-7.
-
(1987)
J Nucl Med
, vol.28
, pp. 1484-1487
-
-
Shih, W.I.1
Markesbery, W.R.2
Clark, D.B.3
-
74
-
-
0024565039
-
Combined neurophysiological studies in creutzfeldt-jakob disease: A case report
-
Aguglia U, Oliveri RL, Gambardella A, Zappia M, Quattrone A. Combined neurophysiological studies in Creutzfeldt-Jakob disease: a case report. Clin Electroencephalogr 1989; 20: 103-10.
-
(1989)
Clin Electroencephalogr
, vol.20
, pp. 103-110
-
-
Aguglia, U.1
Oliveri, R.L.2
Gambardella, A.3
Zappia, M.4
Quattrone, A.5
-
75
-
-
0027329195
-
Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in creutzfeldt-jakob disease
-
Aguglia U, Oliveri RL, Gambardella A, Quattrone A. Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in Creutzfeldt-Jakob disease. J NeuroI 1993; 240: 25-7.
-
(1993)
J Neuroi
, vol.240
, pp. 25-27
-
-
Aguglia, U.1
Oliveri, R.L.2
Gambardella, A.3
Quattrone, A.4
-
76
-
-
0019514305
-
Panencephalopathic type of creutzfeldt-jakob disease: Primary involvement of the cerebral white matter
-
Mizutani T, Okumura A, Oda M, Shiraki H. Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter. J Neurol Neurosurg Psychiatry 1981; 44: 103-15.
-
(1981)
J Neurol Neurosurg Psychiatry
, vol.44
, pp. 103-115
-
-
Mizutani, T.1
Okumura, A.2
Oda, M.3
Shiraki, H.4
-
77
-
-
0025210356
-
Panencephalopathic type of creutzfeldt-jakob disease with primary extensive involvement of white matter
-
Kruger H, Meesmann C Rohrbach E, Muller I, Mertens HG. Panencephalopathic type of Creutzfeldt-Jakob disease with primary extensive involvement of white matter. Eur Neurol 1990; 30: 115-9.
-
(1990)
Eur Neurol
, vol.30
, pp. 115-119
-
-
Kruger, H.1
Meesmann C Rohrbach, E.2
Muller, I.3
Mertens, H.G.4
-
78
-
-
0028946529
-
Inherited creutfeldt-jakob disease in a british family associated with a novel 144 base pair insertion of the prion protein gene
-
Nicholl D, Windl O, De Silva R, Inherited Creutfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene. J Neurol Neurosurg Psychiatry 1995; 58: 65-9.
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 65-69
-
-
Nicholl, D.1
Windl, O.2
De Silva, R.3
-
79
-
-
0023735496
-
A new case of creutzfeldt-jakob disease associated with human growth hormone therapy in new zealand
-
Croxson M, Brown P, Synek B, A new case of Creutzfeldt-Jakob disease associated with human growth hormone therapy in New Zealand. Neurology 1988; 38: 1128-30.
-
(1988)
Neurology
, vol.38
, pp. 1128-1130
-
-
Croxson, M.1
Brown, P.2
Synek, B.3
-
80
-
-
0027518835
-
Creutzfeldt-jakob disease transmitted by cadaveric dural graft: A case report
-
Takayama S, Hatsuda N, Matsumura K, Nakasu S, Handa J. Creutzfeldt-Jakob disease transmitted by cadaveric dural graft: a case report. No Shinkei Geka-Neurol Surg 1993; 21: 167-70.
-
(1993)
No Shinkei Geka-Neurol Surg
, vol.21
, pp. 167-170
-
-
Takayama, S.1
Hatsuda, N.2
Matsumura, K.3
Nakasu, S.4
Handa, J.5
-
81
-
-
0028202170
-
Creutzfeldt-jakob disease in a pregnant woman with an implanted dura mater graft
-
Lane KL, Brown P, Howell DN, Creutzfeldt-Jakob disease in a pregnant woman with an implanted dura mater graft. Neurosurgery 1994; 34: 737-40.
-
(1994)
Neurosurgery
, vol.34
, pp. 737-740
-
-
Lane, K.L.1
Brown, P.2
Howell, D.N.3
-
82
-
-
0028662447
-
Accidental transmission of creutzfeldt-jakob disease by dural cadaveric grafts
-
Martinez-Lage JF, Poza M, Sola J, Accidental transmission of Creutzfeldt-Jakob disease by dural cadaveric grafts. J Neurol Neurosurg Psychiatry 1994; 57: 1091-4.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 1091-1094
-
-
Martinez-Lage, J.F.1
Poza, M.2
Sola, J.3
-
83
-
-
0031455907
-
Creutzfeldt-jakob disease with a widespread presence of kuru-type plaques after cadaveric dural graft replacement: An autopsy case [abstract]
-
Takashima S, Tateishi I, Taguchi Y, Creutzfeldt-Jakob disease with a widespread presence of kuru-type plaques after cadaveric dural graft replacement: an autopsy case [abstract]. Rinsho Shinkeigaku-Clin NeuroI 1997; 37: 824-8.
-
(1997)
Rinsho Shinkeigaku-Clin Neuroi
, vol.37
, pp. 824-828
-
-
Takashima, S.1
Tateishi, I.2
Taguchi, Y.3
-
84
-
-
0030864494
-
Panencephalopathic type of creutzfeldt-jakob disease associated with cadaveric dura mater graft
-
Yamada M, Itoh Y, Suematsu N, Matsushita M, Otomo E. Panencephalopathic type of Creutzfeldt-Jakob disease associated with cadaveric dura mater graft. J Neurol Neurosurg Psychiatry 1997; 63: 524-7.
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.63
, pp. 524-527
-
-
Yamada, M.1
Itoh, Y.2
Suematsu, N.3
Matsushita, M.4
Otomo, E.5
-
85
-
-
0019375501
-
Morbus gerstmann-straussler-scheinker. Familie sch.-ein bericht uber drei kranke
-
Schumm F, Boellard JW, Schlote W, StOhr M. Morbus Gerstmann-Straussler-Scheinker. Familie Sch.-Ein Bericht uber drei Kranke. Arch Psych Nervenk 1981; 230: 179-96.
-
(1981)
Arch Psych Nervenk
, vol.230
, pp. 179-196
-
-
Schumm, F.1
Boellard, J.W.2
Schlote, W.3
StOhr, M.4
-
86
-
-
0016170093
-
The ataxic (Cerebellar) form of creutzfeldt-jakob disease
-
Jellinger K, Heiss W-D, Deisenhammer E. The ataxic (cerebellar) form of Creutzfeldt-Jakob disease. J Neurol 1974; 207: 289-305.
-
(1974)
J Neurol
, vol.207
, pp. 289-305
-
-
Jellinger, K.1
Heiss, W.-D.2
Deisenhammer, E.3
-
87
-
-
0025335415
-
Progressive fatal dementia (Creutzfeldt-jakob disease) in a patient who received homograft tissue for tympanic membrane closure
-
Tange RA, Troost D, Limburg M. Progressive fatal dementia (Creutzfeldt-Jakob disease) in a patient who received homograft tissue for tympanic membrane closure. Eur Arch Oto-Rhino-Laryngol 1990; 247: 199-201.
-
(1990)
Eur Arch Oto-Rhino-Laryngol
, vol.247
, pp. 199-201
-
-
Tange, R.A.1
Troost, D.2
Limburg, M.3
-
88
-
-
0027186217
-
Creutzfeldt-jakob disease and lyophilised dura mater grafts: Report of two cases
-
Esmonde T, Lueck CJ, Symon L, Duchen LW, Will RG. Creutzfeldt-Jakob disease and lyophilised dura mater grafts: report of two cases. J Neurol Neurosurg Psychiatry 1993; 56: 999-1000.
-
(1993)
J Neurol Neurosurg Psychiatry
, vol.56
, pp. 999-1000
-
-
Esmonde, T.1
Lueck, C.J.2
Symon, L.3
Duchen, L.W.4
Will, R.G.5
-
89
-
-
0016388150
-
Beitrag zur familiaren spongiosen glio-neuralen dystrophie
-
Bohnert B, Noetzel H. Beitrag zur familiaren spongiosen glio-neuralen Dystrophie. Arch Psych Nervenk 1974; 218: 353.
-
(1974)
Arch Psych Nervenk
, vol.218
, pp. 353
-
-
Bohnert, B.1
Noetzel, H.2
-
90
-
-
0031594134
-
Mri in sporadic creutzfeldt-jakob disease: Correlation with clinical and neuropathological data
-
Urbach H, Klisch J, Wolf HK, Brechtelsbauer D, Gass S, Solymosi I. 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
Brechtelsbauer, D.4
Gass, S.5
Solymosi, I.6
-
91
-
-
0029665780
-
Pohl c bender h, 18f_ fluorodeoxyglucose-pet and 99mtc-bicisate-spect in creutzfeldt-jakob disease
-
Grunwald F, Pohl C Bender H, 18F_ fluorodeoxyglucose-PET and 99mTc-bicisate-SPECT in Creutzfeldt-Jakob disease. Ann Nucl Med 1996; 10: 131-4.
-
(1996)
Ann Nucl Med
, vol.10
, pp. 131-134
-
-
Grunwald, F.1
-
92
-
-
0029790194
-
Creutzfeldt-jakob disease in a beef farmer
-
Young GR, Fletcher NA, Zeidler M, Estibeiro KL, Ironside JW. Creutzfeldt-Jakob disease in a beef farmer. Lancet 1996; 348: 610-1.
-
(1996)
Lancet
, vol.348
, pp. 610-611
-
-
Young, G.R.1
Fletcher, N.A.2
Zeidler, M.3
Estibeiro, K.L.4
Ironside, J.W.5
-
93
-
-
17944389280
-
Evolution electroencephalographique de deux cas de syndrome de creutzfeldt-jakob tardifs
-
Hauser-Dumur F, Radvanyi MF. Evolution electroencephalographique de deux cas de syndrome de Creutzfeldt-Jakob tardifs. Rev Neurol (Paris) 1969; 121: 241-4.
-
(1969)
Rev Neurol
, vol.121
, pp. 241-244
-
-
Hauser-Dumur, F.1
Radvanyi, M.F.2
-
95
-
-
0015699556
-
Evolution of eeg and visual evoked response changes in jakob-creutzfeldt disease
-
Lee RG, Blair RDG. Evolution of EEG and visual evoked response changes in Jakob-Creutzfeldt disease. EEG Clin Neurophysiol 1973; 35: 133-42.
-
(1973)
EEG Clin Neurophysiol
, vol.35
, pp. 133-142
-
-
Lee, R.G.1
Blair, R.D.G.2
-
96
-
-
0019175731
-
Creutzfeldt-jakob disease with extensive degeneration of white matter
-
Park TS, Kleinman GM, Richardson EP. Creutzfeldt-Jakob disease with extensive degeneration of white matter. Acta Neuropathol (Berlin) 1980; 52: 239-42.
-
(1980)
Acta Neuropathol
, vol.52
, pp. 239-242
-
-
Park, T.S.1
Kleinman, G.M.2
Richardson, E.P.3
-
97
-
-
0022681325
-
Forma de heidenhain da doenca de creutzfeldt-jakob: Relato de urn caso
-
Pinto Junior LR, Lancelloti CL, Nozuka AP, Andivar AP, Anvito WL. Forma de Heidenhain da doenca de Creutzfeldt-Jakob: relato de urn caso. Arquivos de NeuroPsiquiatria 1986; 44: 60-6.
-
(1986)
Arquivos De Neuropsiquiatria
, vol.44
, pp. 60-66
-
-
Pinto Junior, L.R.1
Lancelloti, C.L.2
Nozuka, A.P.3
Ivar, A.P.4
Anvito, W.L.5
-
98
-
-
0022591987
-
Electrophysiological and pathological studies on creutzfeldt-jakob disease with retinal involvement
-
Tsutsui J, Kawashima S, Kajikawa I, Shirabe T, Terao A. Electrophysiological and pathological studies on Creutzfeldt-Jakob disease with retinal involvement. Doc Ophthalmol 1986; 63: 13-21.
-
(1986)
Doc Ophthalmol
, vol.63
, pp. 13-21
-
-
Tsutsui, J.1
Kawashima, S.2
Kajikawa, I.3
Shirabe, T.4
Terao, A.5
-
99
-
-
0025032319
-
Positron emission tomography in creutzfeldt-jakob disease
-
Holthoff VA, Sandmann J, Pawlik G, Schroder R, Heiss WD. Positron emission tomography in Creutzfeldt-Jakob disease. Arch Neurol 1990; 47: 1035-8.
-
(1990)
Arch Neurol
, vol.47
, pp. 1035-1038
-
-
Holthoff, V.A.1
Sandmann, J.2
Pawlik, G.3
Schroder, R.4
Heiss, W.D.5
-
100
-
-
0028271365
-
Posterior cortical atrophy: Neuropathologic correlations
-
Victoroff J, Ross GW, Benson DF, Verity MA, Vinters HV. Posterior cortical atrophy: neuropathologic correlations. Arch Neurol 1994; 51: 269-74.
-
(1994)
Arch Neurol
, vol.51
, pp. 269-274
-
-
Victoroff, J.1
Ross, G.W.2
Benson, D.F.3
Verity, M.A.4
Vinters, H.V.5
-
101
-
-
0032231313
-
The role of 99mtc_ hmpao spect in the diagnosis of creutzfeldt-jacob disease
-
Miller DA, Vitti RA, Maslack MM. The role of 99mTc_ HMPAO SPECT in the diagnosis of Creutzfeldt-Jacob disease. Am J Neuroradiol 1998; 19: 454-5.
-
(1998)
Am J Neuroradiol
, vol.19
, pp. 454-455
-
-
Miller, D.A.1
Vitti, R.A.2
Maslack, M.M.3
-
102
-
-
0026606082
-
Atypical creutzfeldt-jakob disease in an american family with an insert mutation in the prnp amyloid precursor gene
-
Brown P, Goldfarb LG, McCombie WR, Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene. Neurology 1992; 42: 422-7.
-
(1992)
Neurology
, vol.42
, pp. 422-427
-
-
Brown, P.1
Goldfarb, L.G.2
McCombie, W.R.3
-
103
-
-
0027363964
-
A new (Two repeat) octapeptide coding insert mutation in creutzfeldt-jakob disease
-
Goldfarb LG, Brown P, Little BW, A new (two repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease. Neurology 1993; 43: 2392-4.
-
(1993)
Neurology
, vol.43
, pp. 2392-2394
-
-
Goldfarb, L.G.1
Brown, P.2
Little, B.W.3
-
104
-
-
0027443351
-
Clinical heterogeneity and unusual presentations of creutzfeldt-jakob disease in jewish patients with the prnp codon 200 mutation
-
Chapman J, Brown P, Goldfarb LG, Arlazoroff A, Gajdusek DC, Korczyn AD. Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. J Neurol Neurosurg Psychiatry 1993; 56: 1109-12.
-
(1993)
J Neurol Neurosurg Psychiatry
, vol.56
, pp. 1109-1112
-
-
Chapman, J.1
Brown, P.2
Goldfarb, L.G.3
Arlazoroff, A.4
Gajdusek, D.C.5
Korczyn, A.D.6
-
105
-
-
0033594504
-
Of right-hemisphere dysfunction in creutzfeldt-jakob disease
-
Yee AS, Simon JH, Anderson CA, Sze C-I, Filley CM. Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease. Neurology 1999; 52: 1514.
-
(1999)
Neurology
, vol.52
, pp. 1514
-
-
Yee, A.S.1
Simon, J.H.2
Erson, C.A.3
Sze, C.-I.4
Filley, C.M.5
Diffusion-Weighted, M.6
-
106
-
-
17744408285
-
Is applanation tonometry a risk factor for transmission of creutzfeldt-jakob disease?
-
Rizzo M, Corbett JJ, Thompson HS. Is applanation tonometry a risk factor for transmission of Creutzfeldt-Jakob disease? Arch Ophthalmol 1987; 105: 314.
-
(1987)
Arch Ophthalmol
, vol.105
, pp. 314
-
-
Rizzo, M.1
Corbett, J.J.2
Thompson, H.S.3
-
107
-
-
0014383577
-
Creutzfeldt-jakob disease 1 survey of the literature and clinical diagnosis
-
May WW. Creutzfeldt-Jakob disease 1 Survey of the literature and clinical diagnosis. Acta Neurol Scand 1968; 44: 1-32.
-
(1968)
Acta Neurol Scand
, vol.44
, pp. 1-32
-
-
May, W.W.1
-
108
-
-
17944394267
-
Sur l'unite histopathologique des encephalopathies subaigues (Types creutzfeldt-jakob, heidenhain et nevin)
-
Lafon R, Labauge R, van Bogaert L, Castan P. Sur l'unite histopathologique des encephalopathies subaigues (types Creutzfeldt-Jakob, Heidenhain et Nevin). Rev Neurol (Paris) 1965; 112: 201-27.
-
(1965)
Rev Neurol
, vol.112
, pp. 201-227
-
-
Lafon, R.1
Labauge, R.2
Van Bogaert, L.3
Castan, P.4
-
109
-
-
0018794278
-
Two neurological cases. Demonstration at the royal college of physicians of london
-
Matthews WB, Hyman NM, Bannister R, Trevor Hughes J, Pyke DA, Milne MD. Two neurological cases. Demonstration at the Royal College of Physicians of London. BMJ 1979; 1: 727-32.
-
(1979)
BMJ
, vol.1
, pp. 727-732
-
-
Matthews, W.B.1
Hyman, N.M.2
Bannister, R.3
Trevor Hughes, J.4
Pyke, D.A.5
Milne, M.D.6
-
110
-
-
0023841066
-
Creutzfeldt-jakob disease in histopathology technicians
-
Sitwell L, Lach B, Atack E, Atack D, Izukawa D. Creutzfeldt-Jakob disease in histopathology technicians. N Engl J Med 1988; 318: 854.
-
(1988)
N Engl J Med
, vol.318
, pp. 854
-
-
Sitwell, L.1
Lach, B.2
Atack, E.3
Atack, D.4
Izukawa, D.5
-
111
-
-
0032198049
-
Creutzfeldt-jakob disease presenting with visual blurring, diplopia and visual loss: Heidenhain's variant
-
Lee KE, Loh NK, Tan AK, Tija HT. Creutzfeldt-Jakob disease presenting with visual blurring, diplopia and visual loss: Heidenhain's variant. Ann Acad Med Singapore 1998; 27: 85.
-
(1998)
Ann Acad Med Singapore
, vol.27
, pp. 85
-
-
Lee, K.E.1
Loh, N.K.2
Tan, A.K.3
Tija, H.T.4
-
112
-
-
0021083958
-
Case records of the massachusetts general hospital. Case 49-1983
-
Schneck SA, Hedley-White ET. Case records of the Massachusetts General Hospital. Case 49-1983. N Engl J Med 1983; 309: 1440-9.
-
(1983)
N Engl J Med
, vol.309
, pp. 1440-1449
-
-
Schneck, S.A.1
Hedley-White, E.T.2
-
113
-
-
0022653853
-
Early evolution and incidence of electroencephalographic abnormalities in creutzfeldt-jakob disease
-
Levy SR, Chiappa KH, Burke CJ, Young RR. Early evolution and incidence of electroencephalographic abnormalities in Creutzfeldt-Jakob disease. J Clin Neurophysiol 1986; 3: 1-21.
-
(1986)
J Clin Neurophysiol
, vol.3
, pp. 1-21
-
-
Levy, S.R.1
Chiappa, K.H.2
Burke, C.J.3
Young, R.R.4
-
114
-
-
0028046489
-
Unilateral creutzfeldt-jakob disease presenting as rapidly progressive aphasia
-
Kirk A, Ang LC. Unilateral Creutzfeldt-Jakob disease presenting as rapidly progressive aphasia. Can J Neurol Sci 1994; 21: 350-2.
-
(1994)
Can J Neurol Sci
, vol.21
, pp. 350-352
-
-
Kirk, A.1
Ang, L.C.2
-
115
-
-
0343942139
-
Subacute spongiform encephalopathy: Spongiform cerebral atrophy
-
Christensen E, Brun A. Subacute spongiform encephalopathy: spongiform cerebral atrophy. Neurology 1963; 13: 455-63.
-
(1963)
Neurology
, vol.13
, pp. 455-463
-
-
Christensen, E.1
Brun, A.2
-
116
-
-
18244411422
-
Subakute spongiiise encephalopathie (Jakob-creutzfeldt-syndrom): Klinischmorphologische analyse von 9 fiillen
-
Garzuly F, Jellinger K, Pilz P. Subakute spongiiise Encephalopathie (Jakob-Creutzfeldt-Syndrom): klinischmorphologische Analyse von 9 Fiillen. Arch Psych Nervenk 1971; 214: 207-27.
-
(1971)
Arch Psych Nervenk
, vol.214
, pp. 207-227
-
-
Garzuly, F.1
Jellinger, K.2
Pilz, P.3
-
117
-
-
0016296827
-
Jakob-creutzfe1dt disease: Modification of clinical and electroencephalographic activity with methylphenidate and diazepam
-
Elliott F, Gardner-Thorpe C, Barwick DD, Foster JB. Jakob-Creutzfe1dt disease: modification of clinical and electroencephalographic activity with methylphenidate and diazepam. J Neurol Neurosurg Psychiatry 1974; 37: 879-87.
-
(1974)
J Neurol Neurosurg Psychiatry
, vol.37
, pp. 879-887
-
-
Elliott, F.1
Gardner-Thorpe, C.2
Barwick, D.D.3
Foster, J.B.4
-
118
-
-
0031015974
-
Clinical and diagnostic findings in a patient with creutzfeldt-jakob disease (Type heidenhain)
-
Stafen W, Trinka E, Iglseder B, Pilz P, Homann N, Ladurner G. Clinical and diagnostic findings in a patient with Creutzfeldt-Jakob disease (type Heidenhain). J Neuroimaging 1997; 7: 50-4.
-
(1997)
J Neuroimaging
, vol.7
, pp. 50-54
-
-
Stafen, W.1
Trinka, E.2
Iglseder, B.3
Pilz, P.4
Homann, N.5
Ladurner, G.6
-
119
-
-
0020059994
-
Familial cerebral amyloidosis and spongiform encephalopathy
-
Adam J, Crow TJ, Duchen LW, Scaravilli F, Spokes E. Familial cerebral amyloidosis and spongiform encephalopathy. J Neurol Neurosurg Psychiatry 1982; 45: 37-45.
-
(1982)
J Neurol Neurosurg Psychiatry
, vol.45
, pp. 37-45
-
-
Adam, J.1
Crow, T.J.2
Duchen, L.W.3
Scaravilli, F.4
Spokes, E.5
-
120
-
-
0027404258
-
Inherited prion disease (Prp lysine 200) in britain: Two case reports
-
Collinge J, Palmer MS, Campbell T, Sidle KCL, Carroll D, Harding A. Inherited prion disease (PrP lysine 200) in Britain: two case reports. BMJ 1993; 306: 301-2.
-
(1993)
BMJ
, vol.306
, pp. 301-302
-
-
Collinge, J.1
Palmer, M.S.2
Campbell, T.3
Sidle, K.4
Carroll, D.5
Harding, A.6
-
121
-
-
0024471762
-
Transmission of creutzfeldt-jakob disease by dural cadaveric graft
-
Masullo C, Pocchiari M, Macchi G, Alema G, Piazza G, Panzera MA. Transmission of Creutzfeldt-Jakob disease by dural cadaveric graft. J Neurosurg 1989; 71: 954-5.
-
(1989)
J Neurosurg
, vol.71
, pp. 954-955
-
-
Masullo, C.1
Pocchiari, M.2
Macchi, G.3
Alema, G.4
Piazza, G.5
Panzera, M.A.6
-
122
-
-
0026650443
-
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
-
Collinge J, Brown J, Hardy J, Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. Brain 1992; 115: 687-710.
-
(1992)
Brain
, vol.115
, pp. 687-710
-
-
Collinge, J.1
Brown, J.2
Hardy, J.3
-
123
-
-
0014403570
-
Die subakute encephalopathie creutzfeldt-jakob, eine abiotrophische degeneration des praseniums
-
Kreindler A, Vuia O, Marcutiu V, Alexianu M. Die subakute Encephalopathie Creutzfeldt-Jakob, eine abiotrophische Degeneration des Praseniums. Dtsch Z Nervenheilkd 1968; 193: 351-69.
-
(1968)
Dtsch Z Nervenheilkd
, vol.193
, pp. 351-369
-
-
Kreindler, A.1
Vuia, O.2
Marcutiu, V.3
Alexianu, M.4
-
124
-
-
0017143842
-
Etude electrophysiologique de deux cas de maladie de creutzfeldt-jakob
-
Capon A, Colin F, Deltenre P, Hubert JP, Flament-Durand J. Etude electrophysiologique de deux cas de maladie de Creutzfeldt-Jakob. Rev Encephalogr Neurophysiol Clin 1976; 6: 130-6.
-
(1976)
Rev Encephalogr Neurophysiol Clin
, vol.6
, pp. 130-136
-
-
Capon, A.1
Colin, F.2
Deltenre, P.3
Hubert, J.P.4
Flament-Durand, J.5
-
125
-
-
0017939118
-
Correlations electrophysiologiques, cliniques et anatomiques dans un cas de maladie de creutzfeldt-jakob (Forme de heidenhain)
-
Paty J, Bonnaud E, Latinville D, Correlations electrophysiologiques, cliniques et anatomiques dans un cas de maladie de Creutzfeldt-Jakob (forme de Heidenhain). Rev Neurol (Paris) 1978; 134: 223-31.
-
(1978)
Rev Neurol (Paris)
, vol.134
, pp. 223-231
-
-
Paty, J.1
Bonnaud, E.2
Latinville, D.3
-
126
-
-
0029089215
-
Antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses in creutzfeldt-jakob disease (Heidenhain type): A case study
-
Jibiki I, Fukushima T, Kobayashi K, Aoki T, Yamaguchi N. Antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses in Creutzfeldt-Jakob disease (Heidenhain type): a case study. Psychiatry Clin Neurosci 1995; 49: 87-90.
-
(1995)
Psychiatry Clin Neurosci
, vol.49
, pp. 87-90
-
-
Jibiki, I.1
Fukushima, T.2
Kobayashi, K.3
Aoki, T.4
Yamaguchi, N.5
-
127
-
-
0028245044
-
Reliability of eeg in the diagnosis of creutzfeldt-jakob disease
-
Bortone E, Bettoni L, Giorgi C, Terzano MG, Trabattoni GR, Mancia D. Reliability of EEG in the diagnosis of Creutzfeldt-Jakob disease. EEG Clin Neurophysiol 1994; 90: 323-30.
-
(1994)
EEG Clin Neurophysiol
, vol.90
, pp. 323-330
-
-
Bortone, E.1
Bettoni, L.2
Giorgi, C.3
Terzano, M.G.4
Trabattoni, G.R.5
Mancia, D.6
-
129
-
-
0025083424
-
Pre-mortem diagnosis of creutzfeldt-jakob disease by detection of abnormal cerebrospinal fluid proteins
-
Blisard KS, Davis LE, Harrington MG, Lovell JK, Kornfield M, Berger ML. Pre-mortem diagnosis of Creutzfeldt-Jakob disease by detection of abnormal cerebrospinal fluid proteins. J Neurol Sci 1990; 99: 75-81.
-
(1990)
J Neurol Sci
, vol.99
, pp. 75-81
-
-
Blisard, K.S.1
Davis, L.E.2
Harrington, M.G.3
Lovell, J.K.4
Kornfield, M.5
Berger, M.L.6
-
131
-
-
0031588178
-
New variant creutzfeldt-jakob disease: Neurological features and diagnostic tests
-
Zeidler M, Stewart GE, Barraclough CR, New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests. Lancet 1997; 350: 903-7.
-
(1997)
Lancet
, vol.350
, pp. 903-907
-
-
Zeidler, M.1
Stewart, G.E.2
Barraclough, C.R.3
-
132
-
-
0023212701
-
Subacute spongiform encephalopathy with periodic paroxysmal activities: Clinical evolution and serial eeg findings in 20 cases
-
Aguglia U, Farnarier G, Tinuper P, Rey M, Gomez M, Quattrone A. Subacute spongiform encephalopathy with periodic paroxysmal activities: clinical evolution and serial EEG findings in 20 cases. Clin Electroencephalogr 1987; 18: 147-58.
-
(1987)
Clin Electroencephalogr
, vol.18
, pp. 147-158
-
-
Aguglia, U.1
Farnarier, G.2
Tinuper, P.3
Rey, M.4
Gomez, M.5
Quattrone, A.6
-
133
-
-
0141577719
-
Rapidly progressive cerebral degeneration (Subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy
-
Jones DP, Nevin S. Rapidly progressive cerebral degeneration (subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy. J Neurol Neurosurg Psychiatry 1954; 17: 148-59.
-
(1954)
J Neurol Neurosurg Psychiatry
, vol.17
, pp. 148-159
-
-
Jones, D.P.1
Nevin, S.2
-
134
-
-
0018355447
-
Virussimulating structures in the optic nerve head in creutzfeldt-jakob disease
-
Roth AM, Keltner JL, Ellis WG, Martins-Green M. Virussimulating structures in the optic nerve head in Creutzfeldt-Jakob disease. Am J Ophthalmol 1979; 87: 827-33.
-
(1979)
Am J Ophthalmol
, vol.87
, pp. 827-833
-
-
Roth, A.M.1
Keltner, J.L.2
Ellis, W.G.3
Martins-Green, M.4
-
135
-
-
0019367494
-
Autonomic dysfunction in subacute spongiform encephalopathy
-
Khurana RK, Garcia JH. Autonomic dysfunction in subacute spongiform encephalopathy. Arch Neurol 1981; 38: 114-7.
-
(1981)
Arch Neurol
, vol.38
, pp. 114-117
-
-
Khurana, R.K.1
Garcia, J.H.2
-
136
-
-
0027478766
-
Topodiagnostik der creutzfeldt-jakobschen krankheit durch hmpao-spect
-
Heye N, Farahati J, Heinz A, Buttner T, Przuntek H, Reiners C. Topodiagnostik der Creutzfeldt-Jakobschen Krankheit durch HMPAO-SPECT. Nuklearmedizin 1993; 32: 57-9.
-
(1993)
Nuklearmedizin
, vol.32
, pp. 57-59
-
-
Heye, N.1
Farahati, J.2
Heinz, A.3
Buttner, T.4
Przuntek, H.5
Reiners, C.6
-
137
-
-
0023610378
-
Serial polysornnograrns in creutzfeldt-jakob disease
-
Kazukawa S, Nakamura I, Endo M, Hori A, Inao G. Serial polysornnograrns in Creutzfeldt-Jakob disease. Jpn J Psych Neurol 1987; 41: 651-61.
-
(1987)
Jpn J Psych Neurol
, vol.41
, pp. 651-661
-
-
Kazukawa, S.1
Nakamura, I.2
Endo, M.3
Hori, A.4
Inao, G.5
-
138
-
-
0026575992
-
Creutzfeldt-jakob disease presenting as wernicke-korsakoff syndrome
-
Pietrini W. Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome. J Neurol Sci 1992; 108: 149-53.
-
(1992)
J Neurol Sci
, vol.108
, pp. 149-153
-
-
Pietrini, W.1
-
139
-
-
0027367480
-
Mri abnormalities in creutzfeldt-jakob disease
-
Di Rocco A, Molinari S, Stollman AL, Decker A, Yahr MD. MRI abnormalities in Creutzfeldt-Jakob disease. Neuroradiology 1993; 35: 584-5.
-
(1993)
Neuroradiology
, vol.35
, pp. 584-585
-
-
Di Rocco, A.1
Molinari, S.2
Stollman, A.L.3
Decker, A.4
Yahr, M.D.5
-
140
-
-
0029124766
-
Optische und taktile halluzinose als klinischer beginn einer creutzfeldt-jakob-erkrankung
-
Heinz A, Schmidt LG, Winterer G, Gerhard I, Przuntek H. Optische und taktile Halluzinose als klinischer Beginn einer Creutzfeldt-Jakob-Erkrankung. Nervenarzt 1995; 66: 712-6.
-
(1995)
Nervenarzt
, vol.66
, pp. 712-716
-
-
Heinz, A.1
Schmidt, L.G.2
Winterer, G.3
Gerhard, I.4
Przuntek, H.5
-
141
-
-
0028793550
-
Creutzfeldt-jakob-krankheit. Welche rolle spielt die mr-tomographie
-
Kujat C, Hagen T, Feiden W. Creutzfeldt-Jakob-Krankheit. Welche Rolle spielt die MR-Tomographie? Radiologe 1995; 35: 834-7.
-
(1995)
Radiologe
, vol.35
, pp. 834-837
-
-
Kujat, C.1
Hagen, T.2
Feiden, W.3
-
142
-
-
0031695130
-
A 64-year-old woman with progressive gait disturbance and dementia for one year (Clinical conference) [in japanese]
-
Sugita Y, Matsumine H, Wakiya M, A 64-year-old woman with progressive gait disturbance and dementia for one year (clinical conference) [in Japanese]. No to ShinkeiBrain Nerve 1998; 50: 861-70.
-
(1998)
No to Shinkeibrain Nerve
, vol.50
, pp. 861-870
-
-
Sugita, Y.1
Matsumine, H.2
Wakiya, M.3
-
144
-
-
0023897693
-
A case of creutzfeldt-jakob disease related to familial retinitis pigmentosa patients
-
Mitrova E. A case of Creutzfeldt-Jakob disease related to familial retinitis pigmentosa patients. Eur J Epidemiol 1988; 4: 55-9.
-
(1988)
Eur J Epidemiol
, vol.4
, pp. 55-59
-
-
Mitrova, E.1
-
145
-
-
0024317092
-
Creutzfeldt-jakob disease: High caudate signal on magnetic resonance imaging
-
Pearl GS, Anderson RE. Creutzfeldt-Jakob disease: high caudate signal on magnetic resonance imaging. South Med J 1989; 82: 1177-80.
-
(1989)
South Med J
, vol.82
, pp. 1177-1180
-
-
Pearl, G.S.1
Erson, R.E.2
-
146
-
-
0026787387
-
Creutzfeldt-jakob disease with congophilic kuru plaques: Ct and pathological findings of the cerebral white matter
-
Kawata A, Suga M, Oda M, Hayashi H, Tanabe H. Creutzfeldt-Jakob disease with congophilic kuru plaques: CT and pathological findings of the cerebral white matter. J Neurol Neurosurg Psychiatry 1992; 55: 849-51.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 849-851
-
-
Kawata, A.1
Suga, M.2
Oda, M.3
Hayashi, H.4
Tanabe, H.5
-
147
-
-
0027305995
-
Creutzfeldt-jakob disease in an individual occupationally exposed to bse
-
Davies PTG, Jahfar S, Ferguson IT, Windl O. Creutzfeldt-Jakob disease in an individual occupationally exposed to BSE. Lancet 1993; 342: 680.
-
(1993)
Lancet
, vol.342
, pp. 680
-
-
Davies, P.1
Jahfar, S.2
Ferguson, I.T.3
Windl, O.4
-
148
-
-
0030887492
-
Ataxic type of creutzfeldt-jakob disease with disproportionate enlargement of the fourth ventricle: A serial ct study
-
Berciano J, Pascual J, Polo JM, Combarros O, Figols J, Diez C. Ataxic type of Creutzfeldt-Jakob disease with disproportionate enlargement of the fourth ventricle: a serial CT study. J Neurol Neurosurg Psychiatry 1997; 62: 295-7.
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.62
, pp. 295-297
-
-
Berciano, J.1
Pascual, J.2
Polo, J.M.3
Combarros, O.4
Figols, J.5
Diez, C.6
-
149
-
-
0033573778
-
Investigation of variant creutzfeldt-jakob disease and other human prion diseases with tonsil biopsy samples
-
Hill AF, Butterworth RJ, Joiner S, Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. Lancet 1999; 353: 183-9.
-
(1999)
Lancet
, vol.353
, pp. 183-189
-
-
Hill, A.F.1
Butterworth, R.J.2
Joiner, S.3
-
150
-
-
0028971675
-
Sporadic creutzfeldt-jakob disease in an 18-year-old in the uk
-
Bateman D, Hilton D, Love S, Zeidler M, Beck L Collinge J. Sporadic Creutzfeldt-Jakob disease in an 18-year-old in the UK. Lancet 1995; 346: 1155-6.
-
(1995)
Lancet
, vol.346
, pp. 1155-1156
-
-
Bateman, D.1
Hilton, D.2
Love, S.3
Zeidler, M.4
Beck L Collinge, J.5
-
151
-
-
0031588170
-
New variant creutzfeldt-jakob disease: Psychiatric features
-
Zeidler M, Johnstone EE, Bamber RWK, New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet 1997; 350: 908-10.
-
(1997)
Lancet
, vol.350
, pp. 908-910
-
-
Zeidler, M.1
Johnstone, E.E.2
Bamber, R.3
-
152
-
-
0023646195
-
Rapidly progressive dementia in a patient who received a cadaveric dura mater graft
-
Prichard L Thadani V, Kalb R, Manuelidis E, Hadler J. Rapidly progressive dementia in a patient who received a cadaveric dura mater graft. MMWR 1987; 36: 49-55.
-
(1987)
MMWR
, vol.36
, pp. 49-55
-
-
Prichard L Thadani, V.1
Kalb, R.2
Manuelidis, E.3
Hadler, J.4
-
153
-
-
0023804449
-
Creutzfeldt-jakob disease probably acquired from a cadaveric dura mater graft: Case report
-
Thadani V, Penar PL, Partington L Creutzfeldt-Jakob disease probably acquired from a cadaveric dura mater graft: case report. J Neurosurg 1988; 69: 766-9.
-
(1988)
J Neurosurg
, vol.69
, pp. 766-769
-
-
Thadani, V.1
Penar, P.L.2
Partington, L.3
-
154
-
-
0027257950
-
Pediatric creutzfeldt-jakob disease: Probable transmission by a dural graft
-
Martinez-Lage JF, Sola J, Poza M, Esteban JA. Pediatric Creutzfeldt-Jakob disease: probable transmission by a dural graft. Childs Nerv Syst 1993; 9: 239-42.
-
(1993)
Childs Nerv Syst
, vol.9
, pp. 239-242
-
-
Martinez-Lage, J.F.1
Sola, J.2
Poza, M.3
Esteban, J.A.4
-
155
-
-
0025729704
-
Pituitary growth hormone and creutzfeldt-jakob disease
-
Macario ME, Vaisman M, Buescu A, Moura Neto V, Auaujo HMM, Chagas C. Pituitary growth hormone and Creutzfeldt-Jakob disease. BMJ 1991; 302: 1149.
-
(1991)
BMJ
, vol.302
, pp. 1149
-
-
Macario, M.E.1
Vaisman, M.2
Buescu, A.3
Moura Neto, V.4
Auaujo, H.5
Chagas, C.6
-
157
-
-
0029905230
-
Mutation of the prion protein gene at codon 208 in familial creutzfeldt-jakob disease
-
Mastrianni JA, Iannicola E, Myers RM, DeArmond S, Prusiner SB. Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease. Neurology 1996; 47: 1305-12.
-
(1996)
Neurology
, vol.47
, pp. 1305-1312
-
-
Mastrianni, J.A.1
Iannicola, E.2
Myers, R.M.3
DeArmond, S.4
Prusiner, S.B.5
-
158
-
-
0024324177
-
Familial dementia with prp-positive amyloid plaques: A variant of gerstmann-straussler syndrome
-
Nochlin D, Sumi SM, Bird TD, Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Straussler syndrome. Neurology 1989; 39: 910-8.
-
(1989)
Neurology
, vol.39
, pp. 910-918
-
-
Nochlin, D.1
Sumi, S.M.2
Bird, T.D.3
-
159
-
-
0026563279
-
Fatal familial insomnia: Clinical and pathologic study of five new cases
-
Manetto V, Medori R, Cortelli P, Fatal familial insomnia: clinical and pathologic study of five new cases. Neurology 1992; 42: 312-9.
-
(1992)
Neurology
, vol.42
, pp. 312-319
-
-
Manetto, V.1
Medori, R.2
Cortelli, P.3
-
160
-
-
0026785544
-
Analysis of the prion protein gene in thalamic dementia
-
Petersen RB, Tabaton M, Berg L, Analysis of the prion protein gene in thalamic dementia. Neurology 1992; 42: 1859-63.
-
(1992)
Neurology
, vol.42
, pp. 1859-1863
-
-
Petersen, R.B.1
Tabaton, M.2
Berg, L.3
-
161
-
-
0029961971
-
Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: First report from japan
-
Nagayama M, Shinohara Y, Furukawa H, Kitamoto T. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan. Neurology 1996; 47: 1313-6.
-
(1996)
Neurology
, vol.47
, pp. 1313-1316
-
-
Nagayama, M.1
Shinohara, Y.2
Furukawa, H.3
Kitamoto, T.4
-
162
-
-
0029874720
-
A prion disease with a novel 96-base pair insertional mutation in the prion protein gene
-
Campbell TA, Palmer MS, Will RG, Gibb WRG, Luthert PJ, Collinge J. A prion disease with a novel 96-base pair insertional mutation in the prion protein gene. Neurology 1996; 46: 761-6.
-
(1996)
Neurology
, vol.46
, pp. 761-766
-
-
Campbell, T.A.1
Palmer, M.S.2
Will, R.G.3
Gibb, W.4
Luthert, P.J.5
Collinge, J.6
-
163
-
-
0344342110
-
New variant of creutzfeldt-jakob disease in a 26-year-old french man
-
Chazot G, Broussolle E, Lapras CI, Blattler T, Aguzzi A, Kopp N. New variant of Creutzfeldt-Jakob disease in a 26-year-old French man. Lancet 1996; 347: 1181.
-
(1996)
Lancet
, vol.347
, pp. 1181
-
-
Chazot, G.1
Broussolle, E.2
Lapras, C.I.3
Blattler, T.4
Aguzzi, A.5
Kopp, N.6
-
164
-
-
0027990840
-
Neurophysiological follow-up in two children with creutzfeldt-jakob disease after human growth hormone treatment
-
Richard P, Renault F, Ostre E, Auzoux-Cheve M. Neurophysiological follow-up in two children with Creutzfeldt-Jakob disease after human growth hormone treatment. EEG Clin Neurophysiol 1994; 91: 100-7.
-
(1994)
EEG Clin Neurophysiol
, vol.91
, pp. 100-107
-
-
Richard, P.1
Renault, F.2
Ostre, E.3
Auzoux-Cheve, M.4
-
165
-
-
0031753427
-
An unusual case of creutzfeldt-jakob disease
-
Vingerhoets FJG, Hegyi I, Aguzzi A, Myers P, Pizzolato G, Landis T. An unusual case of Creutzfeldt-Jakob disease. Neurology 1998; 51: 617-9.
-
(1998)
Neurology
, vol.51
, pp. 617-619
-
-
Vingerhoets, F.1
Hegyi, I.2
Aguzzi, A.3
Myers, P.4
Pizzolato, G.5
Landis, T.6
-
166
-
-
0343942506
-
Processus degeneratif atrophique diffus, a predominance thalamostriee. Semeiologie extra-pyramidale et psychique variable. Evolution subaigue a terminaison dementielle
-
Poursines Y, Boudouresques J, Roger J. Processus degeneratif atrophique diffus, a predominance thalamostriee. Semeiologie extra-pyramidale et psychique variable. Evolution subaigue a terminaison dementielle. Rev Neurol (Paris) 1953; 89: 266-71.
-
(1953)
Rev Neurol (Paris)
, vol.89
, pp. 266-271
-
-
Poursines, Y.1
Boudouresques, J.2
Roger, J.3
-
168
-
-
0022545635
-
Encephalopathie d'evolution rapide avec ophtalmoplegie supranucleaire et neuropathie peripherique
-
Brunet P, Viader F, Henin D. Encephalopathie d'evolution rapide avec ophtalmoplegie supranucleaire et neuropathie peripherique. Rev Neurol (Paris) 1986; 142: 159-66.
-
(1986)
Rev Neurol (Paris)
, vol.142
, pp. 159-166
-
-
Brunet, P.1
Viader, F.2
Henin, D.3
-
170
-
-
0019394488
-
Golgi and electronmicroscopic studies of spongiform encephalopathy
-
Landis DMD, Williams RS, Masters CL. Golgi and electronmicroscopic studies of spongiform encephalopathy. Neurology 1981; 31: 538-49.
-
(1981)
Neurology
, vol.31
, pp. 538-549
-
-
Landis, D.1
Williams, R.S.2
Masters, C.L.3
-
171
-
-
0026464707
-
Creutzfeldt-jakob disease in a recipient of human pituitary-derived goandotrophin: A second case
-
Cochius JI, Hyman N, Esiri MM. Creutzfeldt-Jakob disease in a recipient of human pituitary-derived goandotrophin: a second case. J Neurol Neurosurg Psychiatry 1992; 55: 1094-5.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 1094-1095
-
-
Cochius, J.I.1
Hyman, N.2
Esiri, M.M.3
-
172
-
-
0022430022
-
Fatal degenerative neurological disease in patients who received pituitary-derived human growth hormone
-
Hintz R, MacGillivray M, Joy A, Tintner R. Fatal degenerative neurological disease in patients who received pituitary-derived human growth hormone. MMWR 1985; 34: 359-66.
-
(1985)
MMWR
, vol.34
, pp. 359-366
-
-
Hintz, R.1
MacGillivray, M.2
Joy, A.3
Tintner, R.4
-
174
-
-
0026643822
-
Maladie de creutzfeldt-jakob chez quatre enfants traites par hormone de croissance
-
Billette de Villemeur T, Gourmelen M, Beauvais P, Maladie de Creutzfeldt-Jakob chez quatre enfants traites par hormone de croissance. Rev Neurol (Paris) 1992; 148: 328-34.
-
(1992)
Rev Neurol (Paris)
, vol.148
, pp. 328-334
-
-
Billette De Villemeur, T.1
Gourmelen, M.2
Beauvais, P.3
-
175
-
-
0026588465
-
Creutzfeldt-jakob disease in recipients of human growth hormone in the united kingdom: A clinical and radiographic study
-
Marcus HS, Duchen LW, Parkin EM, Creutzfeldt-Jakob disease in recipients of human growth hormone in the United Kingdom: a clinical and radiographic study. Q J Med 1992; 82: 43-51.
-
(1992)
Q J Med
, vol.82
, pp. 43-51
-
-
Marcus, H.S.1
Duchen, L.W.2
Parkin, E.M.3
-
176
-
-
0028211267
-
Iatrogenic creutzfeldt-jakob disease in three growth hormone recipients: A neuropathological study
-
Billette de Villemeur T, Gelot T, Deslys JP, Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study. Neuropathol Appl Neurobiol 1994; 20: 111-7.
-
(1994)
Neuropathol Appl Neurobiol
, vol.20
, pp. 111-117
-
-
Billette De Villemeur, T.1
Gelot, T.2
Deslys, J.P.3
-
178
-
-
0029125679
-
Creutzfeldt-jakob disease after liver transplantation
-
Creange A, Gray F, Cesaro P, Creutzfeldt-Jakob disease after liver transplantation. Ann Neurol 1995; 38: 269-72.
-
(1995)
Ann Neurol
, vol.38
, pp. 269-272
-
-
Creange, A.1
Gray, F.2
Cesaro, P.3
-
179
-
-
0022447484
-
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
-
Lugaresi E, Medori R, Montagna P, Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei. N Engl J Med 1986; 315: 997-1003.
-
(1986)
N Engl J Med
, vol.315
, pp. 997-1003
-
-
Lugaresi, E.1
Medori, R.2
Montagna, P.3
-
181
-
-
0031808607
-
Neuro-ophthalmological aspects of prion diseases
-
Neetens A, Martin JJ. Neuro-ophthalmological aspects of prion diseases. Neuro-ophthalmology 1998; 19: 137-44.
-
(1998)
Neuro-Ophthalmology
, vol.19
, pp. 137-144
-
-
Neetens, A.1
Martin, J.J.2
-
182
-
-
0015290244
-
Subacute spongiform encephalopathy and its relation to jakob-creutzfeldt disease: Report on six cases
-
Goldhammer Y, Bubis JJ, Sarova-Pinhas I, Braham J. Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six cases. J Neurol Neurosurg Psychiatry 1972; 35: 1-10.
-
(1972)
J Neurol Neurosurg Psychiatry
, vol.35
, pp. 1-10
-
-
Goldhammer, Y.1
Bubis, J.J.2
Sarova-Pinhas, I.3
Braham, J.4
-
183
-
-
0018824954
-
Spongiform encephalopathy of long duration: A family study
-
Rice GP A, Paty DW, Ball MJ, Tatham R, Kertesz A. Spongiform encephalopathy of long duration: a family study. Can J Neurol Sci 1980; 7: 171-6.
-
(1980)
Can J Neurol Sci
, vol.7
, pp. 171-176
-
-
Rice, G.1
Paty, D.W.2
Ball, M.J.3
Tatham, R.4
Kertesz, A.5
-
184
-
-
0020532066
-
Maladie de creutzfeldt-jakob ayant evolue 34 mois chez une femme de 26 ans
-
Raverdy P, Hauw JJ, Cathala F, Maladie de Creutzfeldt-Jakob ayant evolue 34 mois chez une femme de 26 ans. Rev Neurol (Paris) 1983; 139: 381-3.
-
(1983)
Rev Neurol (Paris)
, vol.139
, pp. 381-383
-
-
Raverdy, P.1
Hauw, J.J.2
Cathala, F.3
-
185
-
-
0026768838
-
Magnetic resonance imaging follow-up in creutzfeldt-jakob disease
-
Rother J, Schwartz A, Harle M, Wentz KU, Berlit P, Hennerici M. Magnetic resonance imaging follow-up in Creutzfeldt-Jakob disease. J Neurol 1992; 239: 404-6.
-
(1992)
J Neurol
, vol.239
, pp. 404-406
-
-
Rother, J.1
Schwartz, A.2
Harle, M.3
Wentz, K.U.4
Berlit, P.5
Hennerici, M.6
-
186
-
-
0026662717
-
Familial creutzfeldt-jakob disease (Codon 200 mutation) with supranuclear palsy
-
Bertoni JM, Brown P, Goldfarb LG, Rubenstein R, Gajdusek DC. Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy. JAMA 1992; 268: 2413-5.
-
(1992)
JAMA
, vol.268
, pp. 2413-2415
-
-
Bertoni, J.M.1
Brown, P.2
Goldfarb, L.G.3
Rubenstein, R.4
Gajdusek, D.C.5
-
187
-
-
0027258807
-
Dementia associated with a 216 base pair insertion in the prion protein gene: Clinical and neuropathological features
-
Duchen LW, Poulter M, Harding AE. Dementia associated with a 216 base pair insertion in the prion protein gene: clinical and neuropathological features. Brain 1993; 116: 555-657.
-
(1993)
Brain
, vol.116
, pp. 555-657
-
-
Duchen, L.W.1
Poulter, M.2
Harding, A.E.3
-
188
-
-
0018957291
-
Supranuclear palsy of eyelid closure
-
Ross Russell RW. Supranuclear palsy of eyelid closure. Brain 1980; 103: 71-82.
-
(1980)
Brain
, vol.103
, pp. 71-82
-
-
Ross Russell, R.W.1
-
189
-
-
0026349535
-
Geotropic ocular deviation with skew and absence of saccade in creutzfeldt-jacob disease
-
Yokota T, Tsuchiya K, Yamane M, Hayashi M, Tanabe H, Tsukagoshi H. Geotropic ocular deviation with skew and absence of saccade in Creutzfeldt-Jacob disease. J Neurol Sci 1991; 106: 175-8.
-
(1991)
J Neurol Sci
, vol.106
, pp. 175-178
-
-
Yokota, T.1
Tsuchiya, K.2
Yamane, M.3
Hayashi, M.4
Tanabe, H.5
Tsukagoshi, H.6
-
190
-
-
0022363507
-
Creutzfeldt-jakob disease in a young adult with idiopathic hypopituitarism: Possible relation to the administration of cadaveric human growth hormone
-
Koch TK, Berg BO, De Armond SJ, Gravina RF. Creutzfeldt-Jakob disease in a young adult with idiopathic hypopituitarism: possible relation to the administration of cadaveric human growth hormone. N Engl J Med 1985; 313: 731-3.
-
(1985)
N Engl J Med
, vol.313
, pp. 731-733
-
-
Koch, T.K.1
Berg, B.O.2
De Armond, S.J.3
Gravina, R.F.4
-
191
-
-
0021877724
-
Creutzfeldt-jakob disease after administration of human growth hormone
-
Powell-Jackson J, Weller RO, Kennedy P, Preece MA, Whitcombe EM, Newsom-Davis J. Creutzfeldt-Jakob disease after administration of human growth hormone. Lancet 1985; II: 244-6.
-
(1985)
Lancet
, vol.2
, pp. 244-246
-
-
Powell-Jackson, J.1
Weller, R.O.2
Kennedy, P.3
Preece, M.A.4
Whitcombe, E.M.5
Newsom-Davis, J.6
-
192
-
-
0025847996
-
Creutzfeldt-jakob disease in a patient with a cadaveric dural graft
-
Miyashita K, Inuzuka T, Kondo H, Creutzfeldt-Jakob disease in a patient with a cadaveric dural graft. Neurology 1991; 41: 940-1.
-
(1991)
Neurology
, vol.41
, pp. 940-941
-
-
Miyashita, K.1
Inuzuka, T.2
Kondo, H.3
-
193
-
-
0025134309
-
Familial creutzfeldt-jakob disease without periodic eeg activity
-
Tiegn GE, Drury I. Familial Creutzfeldt-Jakob disease without periodic EEG activity. Ann Neurol 1990; 28: 585-8.
-
(1990)
Ann Neurol
, vol.28
, pp. 585-588
-
-
Tiegn, G.E.1
Drury, I.2
-
194
-
-
0018362836
-
Familial creutzfeldt-jakob disease
-
Haltia M, Kovanen J, van Crevel H, Bots GTAM, Stefanko S. Familial Creutzfeldt-Jakob disease. J Neurol Sci 1979; 42: 381-9.
-
(1979)
J Neurol Sci
, vol.42
, pp. 381-389
-
-
Haltia, M.1
Kovanen, J.2
Van Crevel, H.3
Bots, G.4
Stefanko, S.5
-
195
-
-
0018900282
-
Familial creutzfeldt-jakob disease: Autosomal dominance in 14 members over 3 generations
-
Cathala F, Chatelain J, Brown P, Dumas M, Gajdusek DC. Familial Creutzfeldt-Jakob disease: autosomal dominance in 14 members over 3 generations. J Neurol Sci 1980; 47: 343-51.
-
(1980)
J Neurol Sci
, vol.47
, pp. 343-351
-
-
Cathala, F.1
Chatelain, J.2
Brown, P.3
Dumas, M.4
Gajdusek, D.C.5
-
196
-
-
51849178459
-
Ober eine eigenartige hereditar-familiare erkrankung des zentralnervensystems: Zugleich ein beitrag zur frage des vorzeitigen lokalen alterns
-
Gerstrnann J, Straussler E, Scheinker I. Ober eine eigenartige hereditar-familiare Erkrankung des Zentralnervensystems: zugleich ein Beitrag zur Frage des vorzeitigen lokalen Alterns. Z Ges Neurol Psych 1936; 154: 736-802.
-
(1936)
Z Ges Neurol Psych
, vol.154
, pp. 736-802
-
-
Gerstrnann, J.1
Straussler, E.2
Scheinker, I.3
-
197
-
-
0019778656
-
Creutzfeldt-jakob disease virus isolations from the gerstrnann-straussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies
-
Masters CL, Gajdusek DC, Gibbs CJ. Creutzfeldt-Jakob disease virus isolations from the Gerstrnann-Straussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies. Brain 1981; 104: 559-88.
-
(1981)
Brain
, vol.104
, pp. 559-588
-
-
Masters, C.L.1
Gajdusek, D.C.2
Gibbs, C.J.3
-
198
-
-
0024856332
-
Gerstrnann-straussler-scheinker disease. I. Extending the clinical spectrum
-
Farlow MR, Yee RD, Dlouhy SR, Conneally PM, Azzarelli B, Ghetti B. Gerstrnann-Straussler-Scheinker disease. I. Extending the clinical spectrum. Neurology 1989; 39: 1446-52.
-
(1989)
Neurology
, vol.39
, pp. 1446-1452
-
-
Farlow, M.R.1
Yee, R.D.2
Dlouhy, S.R.3
Conneally, P.M.4
Azzarelli, B.5
Ghetti, B.6
-
199
-
-
0026500302
-
Abnormal eye movements in gerstrnann-straussler-scheinker disease
-
Yee RD, Farlow MR, Suzuki DA, Betelak KF, Ghetti B. Abnormal eye movements in Gerstrnann-Straussler-Scheinker disease. Arch Ophthalmol 1992; 110: 68-74.
-
(1992)
Arch Ophthalmol
, vol.110
, pp. 68-74
-
-
Yee, R.D.1
Farlow, M.R.2
Suzuki, D.A.3
Betelak, K.F.4
Ghetti, B.5
-
200
-
-
0342636008
-
Preseniele, subacute, progressieve encefalopathie met status myoclonicus
-
Kramer DW. Preseniele, subacute, progressieve encefalopathie met status myoclonicus. Ned Tijdschr Geneesk 1959; 103: 1662-1676.
-
(1959)
Ned Tijdschr Geneesk
, vol.103
, pp. 1662-1676
-
-
Kramer, D.W.1
-
201
-
-
0031000786
-
The 14-3-3 brain protein and transmissible spongiform encephalopathy
-
Moussavian M, Potolicchio S, Jones R. The 14-3-3 brain protein and transmissible spongiform encephalopathy. N Engl J Med 1997; 336: 873-4.
-
(1997)
N Engl J Med
, vol.336
, pp. 873-874
-
-
Moussavian, M.1
Potolicchio, S.2
Jones, R.3
-
202
-
-
0019774510
-
Slowly alternating skew deviation: Description of a pretectal syndrome in three patients
-
Corbett JJ, Schatz NJ, Schults WT, Behrens M, Berry RG. Slowly alternating skew deviation: description of a pretectal syndrome in three patients. Ann Neurol 1981; 10: 540-565.
-
(1981)
Ann Neurol
, vol.10
, pp. 540-565
-
-
Corbett, J.J.1
Schatz, N.J.2
Schults, W.T.3
Behrens, M.4
Berry, R.G.5
-
203
-
-
0001368147
-
Polyopia and monocular diplopia of cerebral origin
-
Bender MB. Polyopia and monocular diplopia of cerebral origin. Arch Neurol Psychiatry 1945; 54: 323-38.
-
(1945)
Arch Neurol Psychiatry
, vol.54
, pp. 323-338
-
-
Bender, M.B.1
-
205
-
-
78651041685
-
Degenerative disease of the central nervous system in new guinea: The endemic occurrence of 'kuru' in the native population
-
Gajdusek DC, Zigas V. Degenerative disease of the central nervous system in New Guinea: the endemic occurrence of 'kuru' in the native population. N Engl J Med 1957; 257: 974-8.
-
(1957)
N Engl J Med
, vol.257
, pp. 974-978
-
-
Gajdusek, D.C.1
Zigas, V.2
-
206
-
-
0014258955
-
Kuru: Subacute cerebellar degeneration. The natural history and clinical features
-
Hornabrook RW. Kuru: subacute cerebellar degeneration. The natural history and clinical features. Brain 1968; 91: 53-74.
-
(1968)
Brain
, vol.91
, pp. 53-74
-
-
Hornabrook, R.W.1
-
207
-
-
0001362115
-
An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-jakob disease)
-
Brownell B, Oppenheimer DR. An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-Jakob disease). J Neurol Neurosurg Psychiatry 1965; 28: 350-461.
-
(1965)
J Neurol Neurosurg Psychiatry
, vol.28
, pp. 350-461
-
-
Brownell, B.1
Oppenheimer, D.R.2
-
208
-
-
0021967982
-
Ataxic creutzfeldt-jakob disease: Diagnostic techniques and neuropathologic observations in early disease
-
Jones HR, Hedley-White ET, Freidberg SR, Baker RA. Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early disease. Neurology 1985; 35: 254-7.
-
(1985)
Neurology
, vol.35
, pp. 254-257
-
-
Jones, H.R.1
Hedley-White, E.T.2
Freidberg, S.R.3
Baker, R.A.4
-
209
-
-
0022363761
-
Clinical and pathological features and laboratory confirmation of creutzfeldt-jakob disease in a recipient of pituitary-derived human growth hormone
-
Gibbs CJ, Joy A, Heffner R, Clinical and pathological features and laboratory confirmation of Creutzfeldt-Jakob disease in a recipient of pituitary-derived human growth hormone. N Engl J Med 1985; 313: 734-8.
-
(1985)
N Engl J Med
, vol.313
, pp. 734-738
-
-
Gibbs, C.J.1
Joy, A.2
Heffner, R.3
-
210
-
-
0022516883
-
Neuropathologic verification of creutzfeldt-jakob disease in the exhumed american recipient of human pituitary growth hormone: Epidemiologic and pathogenetic implications
-
Tintner R, Brown P, Hedley-White ET, Rappaport EB, Piccardo CP, Gajdusek DC. Neuropathologic verification of Creutzfeldt-Jakob disease in the exhumed American recipient of human pituitary growth hormone: epidemiologic and pathogenetic implications. Neurology 1986; 36: 932-943.
-
(1986)
Neurology
, vol.36
, pp. 932-943
-
-
Tintner, R.1
Brown, P.2
Hedley-White, E.T.3
Rappaport, E.B.4
Piccardo, C.P.5
Gajdusek, D.C.6
-
211
-
-
0023695448
-
Creutzfeldt-jakob disease following pituitaryderived human growth hormone therapy: A new american case
-
Marzewski DJ, Towfighi J, Harrington MG, Merril CR, Brown P. Creutzfeldt-Jakob disease following pituitaryderived human growth hormone therapy: a new American case. Neurology 1988; 38: 1131-3.
-
(1988)
Neurology
, vol.38
, pp. 1131-1133
-
-
Marzewski, D.J.1
Towfighi, J.2
Harrington, M.G.3
Merril, C.R.4
Brown, P.5
-
212
-
-
0023850186
-
Human growth hormone therapy and creutzfeldt-jakob disease: A drama in three acts
-
Brown P. Human growth hormone therapy and Creutzfeldt-Jakob disease: a drama in three acts. Pediatrics 1988; 81: 85-92.
-
(1988)
Pediatrics
, vol.81
, pp. 85-92
-
-
Brown, P.1
-
213
-
-
0025963199
-
Creutzfeldt-jakob disease in pituitary growth hormone recipients in the united states
-
Fradkin JE, Schonberger LB, Mills JL, Creutzfeldt-Jakob disease in pituitary growth hormone recipients in the United States. JAMA 1991; 265: 880-4.
-
(1991)
JAMA
, vol.265
, pp. 880-884
-
-
Fradkin, J.E.1
Schonberger, L.B.2
Mills, J.L.3
-
214
-
-
0027874980
-
Maladie de creutzfeldt-jakob apres traitement par l'hormone de croissance extractive humaine: Etude clinico-pathologique
-
Delisle MB, Fabre N, Rochiccioli P, Doerr-Schott J, Rumeau JL, Bes A. Maladie de Creutzfeldt-Jakob apres traitement par l'hormone de croissance extractive humaine: etude clinico-pathologique. Rev Neurol (Paris) 1993; 149: 524-7.
-
(1993)
Rev Neurol (Paris)
, vol.149
, pp. 524-527
-
-
Delisle, M.B.1
Fabre, N.2
Rochiccioli, P.3
Doerr-Schott, J.4
Rumeau, J.L.5
Bes, A.6
-
215
-
-
0029964292
-
Neurosurgery in a patient with creutzfeldt-jakob disease after pituitary derived growth hormone therapy in childhood
-
Holmes SJ, Ironside JW, Shalet SM. Neurosurgery in a patient with Creutzfeldt-Jakob disease after pituitary derived growth hormone therapy in childhood. J Neurol Neurosurg Psychiatry 1996; 60: 333-5.
-
(1996)
J Neurol Neurosurg Psychiatry
, vol.60
, pp. 333-335
-
-
Holmes, S.J.1
Ironside, J.W.2
Shalet, S.M.3
-
216
-
-
0025221785
-
Creutzfeldt-jakob disease in a recipient of human pituitaryderived gonadotrophin
-
Cochius JI, Mack K, Bums RJ, Alderman CP, Blumbergs PC. Creutzfeldt-Jakob disease in a recipient of human pituitaryderived gonadotrophin. Aust NZ J Med 1990; 20: 592-3.
-
(1990)
Aust NZ J Med
, vol.20
, pp. 592-593
-
-
Cochius, J.I.1
Mack, K.2
Bums, R.J.3
Alderman, C.P.4
Blumbergs, P.C.5
-
217
-
-
0030985004
-
Creutzfeldt-jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma
-
Antoine JE, Michel D, Bertholon P, Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma. Neurology 1997; 48: 1451-3.
-
(1997)
Neurology
, vol.48
, pp. 1451-1453
-
-
Antoine, J.E.1
Michel, D.2
Bertholon, P.3
-
218
-
-
0027730422
-
An israeli family with gerstrnann-straussler-scheinker disease manifesting the codon 102 mutation in the prion protein gene
-
Goldhammer Y, Gabizon R, Meiner Z, Sadeh M. An Israeli family with Gerstrnann-Straussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene. Neurology 1993; 43: 2718-9.
-
(1993)
Neurology
, vol.43
, pp. 2718-2719
-
-
Goldhammer, Y.1
Gabizon, R.2
Meiner, Z.3
Sadeh, M.4
-
219
-
-
9544219691
-
Polymorphism at codon 129 or codon 219 of prnp and clinical heterogeneity in a previously unreported family with gerstrnann-straussler-scheinker disease (Prp-pi02l mutation)
-
Barbanti P, Fabbrini G, Salvatore M, Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstrnann-Straussler-Scheinker disease (PrP-PI02L mutation). Neurology 1996; 47: 734-41.
-
(1996)
Neurology
, vol.47
, pp. 734-741
-
-
Barbanti, P.1
Fabbrini, G.2
Salvatore, M.3
-
220
-
-
0019770729
-
Creutzfeldt-jakobsche krankheit: Das computertomogramm in korrelation zu klinischen, elektroenzephalographischen und neuropathologischen befunden
-
Zieger A, Vonofakos D, Grafin Vitzthum H. Creutzfeldt-Jakobsche Krankheit: das Computertomogramm in Korrelation zu klinischen, elektroenzephalographischen und neuropathologischen Befunden. Nervenarzt 1981; 52: 685-91.
-
(1981)
Nervenarzt
, vol.52
, pp. 685-691
-
-
Zieger, A.1
Vonofakos, D.2
Grafin Vitzthum, H.3
-
221
-
-
0021855007
-
Computed tomography during creutzfeldt-jakob disease
-
Westphal KP, Schachenmayr W. Computed tomography during Creutzfeldt-Jakob disease. Neuroradiology 1985; 27: 362-4.
-
(1985)
Neuroradiology
, vol.27
, pp. 362-364
-
-
Westphal, K.P.1
Schachenmayr, W.2
-
222
-
-
0028235338
-
A case of creutzfeldt-jakob disease presenting with cortical deafness
-
Tobias E, Mann E, Bone I, De Silva R, Ironside J. A case of Creutzfeldt-Jakob disease presenting with cortical deafness. J Neurol Neurosurg Psychiatry 1994; 57: 872-3.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 872-873
-
-
Tobias, E.1
Mann, E.2
Bone, I.3
De Silva, R.4
Ironside, J.5
-
223
-
-
0029083528
-
Centripetal nystagmus in a case of creutzfeldt-jacob disease
-
Helmchen C, Btittner U. Centripetal nystagmus in a case of Creutzfeldt-Jacob disease. Neuro-ophthalmology 1995; 15: 187-92.
-
(1995)
Neuro-Ophthalmology
, vol.15
, pp. 187-192
-
-
Helmchen, C.1
Btittner, U.2
-
224
-
-
0019456903
-
Transmissible spongiform encephalopathy (Creutzfeldt-jakob disease): Atypical clinical and pathological findings
-
Schoene WE, Masters CL, Gibbs CJ, Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease): atypical clinical and pathological findings. Arch Neurol 1981; 38: 473-7.
-
(1981)
Arch Neurol
, vol.38
, pp. 473-477
-
-
Schoene, W.E.1
Masters, C.L.2
Gibbs, C.J.3
-
225
-
-
0031958468
-
Creutzfeldt-jakob disease associated with ocular dipping: A case report
-
Haraguchi T, Akaura K, Yabuki S. Creutzfeldt-Jakob disease associated with ocular dipping: a case report. Rinsho Shinkeigaku-Clin Neurol 1998; 38: 70-73.
-
(1998)
Rinsho Shinkeigaku-Clin Neurol
, vol.38
, pp. 70-73
-
-
Haraguchi, T.1
Akaura, K.2
Yabuki, S.3
-
226
-
-
0026801958
-
A prp gene codon 178 base substitution and a 24-bp interstitial deletion in familial creutzfeldt-jakob disease
-
Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, McLean MJ. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease. Neurology 1992; 42: 1864-70.
-
(1992)
Neurology
, vol.42
, pp. 1864-1870
-
-
Bosque, P.J.1
Vnencak-Jones, C.L.2
Johnson, M.D.3
Whitlock, J.A.4
McLean, M.J.5
-
228
-
-
0028989819
-
Gerstmann-straussler-scheinker disease with mutation at codon 102 and methionine at codon 129 of prnp in previously unreported patients
-
Young K, Jones CK, Piccardo P, Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients. Neurology 1995; 45: 1127-34.
-
(1995)
Neurology
, vol.45
, pp. 1127-1134
-
-
Young, K.1
Jones, C.K.2
Piccardo, P.3
-
229
-
-
0029598460
-
Hypokinesia and presenile dementia in a dutch family with a novel insertion in the prion protein gene
-
van Gool WA, Hensels GW, Hoogerwaard EM, Wiezer JHA, Wesseling P, Bolhuis PA. Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene. Brain 1995; 118: 1565-71.
-
(1995)
Brain
, vol.118
, pp. 1565-1571
-
-
Van Gool, W.A.1
Hensels, G.W.2
Hoogerwaard, E.M.3
Wiezer, J.4
Wesseling, P.5
Bolhuis, P.A.6
-
230
-
-
0027493820
-
Positron emission tomography and histopathology in creutzfeldt-jakob disease
-
Goldman S, Liard A, Flament-Durand J, Positron emission tomography and histopathology in Creutzfeldt-Jakob disease. Neurology 1993; 43: 1828-30.
-
(1993)
Neurology
, vol.43
, pp. 1828-1830
-
-
Goldman, S.1
Liard, A.2
Flament-Durand, J.3
-
231
-
-
0030765818
-
Magnetic resonance imaging in creutzfeldt-jakob disease: Evidence of focal involvement of the cortex
-
Schwaninger M, Winter R, Hacke W, Magnetic resonance imaging in Creutzfeldt-Jakob disease: evidence of focal involvement of the cortex. J Neurol Neurosurg Psychiatry 1997; 63: 408-9.
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.63
, pp. 408-409
-
-
Schwaninger, M.1
Winter, R.2
Hacke, W.3
-
232
-
-
0017040029
-
Analysis of clinical and electrophysiological findings in jakob-creutzfeldt disease
-
Szirmai I, Guseo A, Czopf J, Palffy G. Analysis of clinical and electrophysiological findings in Jakob-Creutzfeldt disease. Arch Psychiatr Nervenk 1976; 222: 315-23.
-
(1976)
Arch Psychiatr Nervenk
, vol.222
, pp. 315-323
-
-
Szirmai, I.1
Guseo, A.2
Czopf, J.3
Palffy, G.4
-
233
-
-
0021127785
-
Bitemporal hypometabolism in creutzfeldt-jakob disease measured by positron emission tomography with [18fl-2-fluorodeoxyglucose
-
Friedland RP, Prusiner SB, Jagust WI, Budinger TF, Davis RL. Bitemporal hypometabolism in Creutzfeldt-Jakob disease measured by positron emission tomography with [18Fl-2-fluorodeoxyglucose. J Comput Assist Tomogr 1984; 8: 978-81.
-
(1984)
J Comput Assist Tomogr
, vol.8
, pp. 978-981
-
-
Friedland, R.P.1
Prusiner, S.B.2
Jagust, W.I.3
Budinger, T.F.4
Davis, R.L.5
-
234
-
-
0025855336
-
Different susceptibilities of the geniculate and extrageniculate visual pathways to human creutzfeldt-jakob disease (A combined neurophysiologicalneuropathological study)
-
Aguglia U, Gambarelli D, Farnarier G, Quattrone A. Different susceptibilities of the geniculate and extrageniculate visual pathways to human Creutzfeldt-Jakob disease (a combined neurophysiologicalneuropathological study). Electroencephalogr Clin Neurophysiol 1991; 78: 413-23.
-
(1991)
Electroencephalogr Clin Neurophysiol
, vol.78
, pp. 413-423
-
-
Aguglia, U.1
Gambarelli, D.2
Farnarier, G.3
Quattrone, A.4
-
235
-
-
0031693769
-
Creutzfeldt-jakob disease. Neurophysiologic visual impairments
-
de Seze J, Hache JC, Vermersch P, Creutzfeldt-Jakob disease. Neurophysiologic visual impairments. Neurology 1998; 51: 962-7.
-
(1998)
Neurology
, vol.51
, pp. 962-967
-
-
De Seze, J.1
Hache, J.C.2
Vermersch, P.3
-
236
-
-
0015165989
-
Unusual electroencephalographic and clinical evolution of a case of meningioma of the left temporo-occipital convexity
-
Gaches J, Supino-Viterbo V, Oughourlian JM. Unusual electroencephalographic and clinical evolution of a case of meningioma of the left temporo-occipital convexity. Eur Neurol 1971; 5: 155-64.
-
(1971)
Eur Neurol
, vol.5
, pp. 155-164
-
-
Gaches, J.1
Supino-Viterbo, V.2
Oughourlian, J.M.3
-
237
-
-
0015090897
-
Retinopathy in sheep affected with natural scrapie
-
Barnett KC, Palmer AC. Retinopathy in sheep affected with natural scrapie. Res Vet Sci 1971; 12: 383-5.
-
(1971)
Res Vet Sci
, vol.12
, pp. 383-385
-
-
Barnett, K.C.1
Palmer, A.C.2
-
239
-
-
0019351880
-
Progressive retinal degeneration in scrapie-infected hamsters: A light and electron microscopic analysis
-
Hogan RN, Baringer JR, Prusiner SB. Progressive retinal degeneration in scrapie-infected hamsters: a light and electron microscopic analysis. Lab Invest 1981; 44: 34-42.
-
(1981)
Lab Invest
, vol.44
, pp. 34-42
-
-
Hogan, R.N.1
Baringer, J.R.2
Prusiner, S.B.3
-
241
-
-
0021858470
-
Retinal degeneration in experimental scrapie after intraperitoneal or subcutaneous inoculation of hamsters
-
Buyukmihci N, Goering-Harmon F, Marsh RF. Retinal degeneration in experimental scrapie after intraperitoneal or subcutaneous inoculation of hamsters. Exp Neurol 1985; 88: 461-6.
-
(1985)
Exp Neurol
, vol.88
, pp. 461-466
-
-
Buyukmihci, N.1
Goering-Harmon, F.2
Marsh, R.F.3
-
242
-
-
0022899080
-
Replication of scrapie prions in hamster eyes precedes retinal degeneration
-
Hogan RN, Bowman KA, Baringer JR, Prusiner SB. Replication of scrapie prions in hamster eyes precedes retinal degeneration. Ophthalmic Res 1986; 18: 230-5.
-
(1986)
Ophthalmic Res
, vol.18
, pp. 230-235
-
-
Hogan, R.N.1
Bowman, K.A.2
Baringer, J.R.3
Prusiner, S.B.4
-
243
-
-
0031292492
-
Electron microscopic studies of the optic nerve in experimental scrapie and the panencephalopathic type of creutzfeldt-jakob disease
-
Walis A, Liberski PP, Brown P, Gajdusek DC. Electron microscopic studies of the optic nerve in experimental scrapie and the panencephalopathic type of Creutzfeldt-Jakob disease. Fol Neuropathol 1997; 35: 255-8.
-
(1997)
Fol Neuropathol
, vol.35
, pp. 255-258
-
-
Walis, A.1
Liberski, P.P.2
Brown, P.3
Gajdusek, D.C.4
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