Prion protein is not detectable in dental pulp from patients with Creutzfeldt-Jakob disease

被引:23
|
作者
Blanquet-Grossard, F
Sazdovitch, V
Jean, A
Deslys, JP
Dormont, D
Hauw, JJ
Marion, D
Brown, P
Cesbron, JY
机构
[1] CNRS, IBL, F-59021 Lille, France
[2] HP Pitie Salpetriere, Neuropathol Lab, F-75651 Paris 13, France
[3] Fac Chirurg Dent, Dept Ontol Conservatrice Endodontie, F-44042 Nantes 1, France
[4] CEA, Lab Neurovirol & Neuropathol Expt, F-92265 Fontenay Aux Roses, France
[5] NINDS, Cent Nervous Syst Studies Lab, NIH, Bethesda, MD 20892 USA
关键词
Creutzfeldt-Jacob disease; prion; dentistry; iatrogenic contamination;
D O I
10.1177/00220345000790020101
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
引用
收藏
页码:700 / 700
页数:1
相关论文
共 50 条
  • [1] Prion protein immunohistochemistry in Creutzfeldt-Jakob disease.
    Giaccone, G
    Canciani, B
    Rossi, G
    Porro, M
    Tagliavini, F
    Bugiani, O
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1998, 57 (05): : 493 - 493
  • [2] Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease
    Glatzel, M
    Abela, E
    Maissen, M
    Aguzzi, A
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (19): : 1812 - 1820
  • [3] Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease
    Armstrong, RA
    Cairns, NJ
    Lantos, PL
    [J]. NEUROPATHOLOGY, 2001, 21 (01) : 19 - 24
  • [4] INSERTION IN PRION PROTEIN GENE IN FAMILIAL CREUTZFELDT-JAKOB DISEASE
    OWEN, F
    LOFTHOUSE, R
    CROW, TJ
    BAKER, HF
    HSIAO, K
    POULTER, M
    COLLINGE, J
    RISBY, D
    RIDLEY, RM
    PRUSINER, SB
    [J]. LANCET, 1989, 1 (8628): : 51 - 52
  • [5] MUTATION OF THE PRION PROTEIN IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB DISEASE
    HSIAO, K
    MEINER, Z
    KAHANA, E
    CASS, C
    KAHANA, I
    AVRAHAMI, D
    SCARLATO, G
    ABRAMSKY, O
    PRUSINER, SB
    GABIZON, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (16): : 1091 - 1097
  • [6] Type of prion protein in UK farmers with Creutzfeldt-Jakob disease
    Hill, AF
    Will, RG
    Ironside, J
    Collinge, J
    [J]. LANCET, 1997, 350 (9072): : 188 - 188
  • [7] Novel prion protein conformation and glycotype in Creutzfeldt-Jakob disease
    Zanusso, Gianluigi
    Polo, Alberto
    Farinazzo, Alessia
    Nonno, Romolo
    Cardone, Franco
    Di Bari, Michele
    Ferrari, Sergio
    Principe, Serena
    Gelati, Matteo
    Fasoli, Elisa
    Fiorini, Michele
    Prelli, Frances
    Frangione, Blas
    Tridente, Giuseppe
    Bentivoglio, Marina
    Giorgi, Alessandra
    Schinina, Maria Eugenia
    Maras, Bruno
    Agrimi, Umberto
    Rizzuto, Nicola
    Pocchiari, Maurizio
    Monaco, Salvatore
    [J]. ARCHIVES OF NEUROLOGY, 2007, 64 (04) : 595 - 599
  • [8] Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease
    Head, MW
    Northcott, V
    Rennison, K
    Ritchie, D
    McCardle, L
    Bunn, TJR
    McLennan, NF
    Ironside, JW
    Tullo, AB
    Bonshek, RE
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (01) : 342 - 346
  • [9] Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients
    Cardone, F
    Liu, QG
    Petraroli, R
    Ladogana, A
    D'Alessandro, M
    Arpino, C
    Di Bari, M
    Macchi, G
    Pocchiari, M
    [J]. BRAIN RESEARCH BULLETIN, 1999, 49 (06) : 429 - 433
  • [10] MUTATION OF THE PRION PROTEIN IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB DISEASE
    DREYFUS, JC
    [J]. M S-MEDECINE SCIENCES, 1991, 7 (06): : 626 - 627