Aguzzi A - Search Results

1

Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein gene.

Frontzek K, Moos R, Schaper E, Jann L, Herfs G, Zimmermann DR, Aguzzi A, Budka H. Frontzek K, et al. Among authors: aguzzi a. Prion. 2015;9(6):444-8. doi: 10.1080/19336896.2015.1121356. Prion. 2015. PMID: 26634863 Free PMC article.

2

Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Collinge J, Diringer H, Gullotta F, Haltia M, Hauw JJ. Budka H, et al. Among authors: aguzzi a. Brain Pathol. 1995 Jul;5(3):319-22. doi: 10.1111/j.1750-3639.1995.tb00609.x. Brain Pathol. 1995. PMID: 8520732 Review.

3

[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action].

Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Collinge J, Diringer H, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Kretzschmar HA, Lantos PL, Masullo C, Pocchiari M, Schlote W, Tateishi J, Will RG. Budka H, et al. Among authors: aguzzi a. Pathologe. 1996 Mar;17(2):171-5. Pathologe. 1996. PMID: 8650149 Review. German.

4

Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Jellinger K, et al. Budka H, et al. Among authors: aguzzi a. Brain Pathol. 1995 Oct;5(4):459-66. doi: 10.1111/j.1750-3639.1995.tb00625.x. Brain Pathol. 1995. PMID: 8974629

5

The use of transgenic mice in the investigation of transmissible spongiform encephalopathies.

Weissmann C, Fischer M, Raeber A, Büeler H, Sailer A, Shmerling D, Rülicke T, Brandner S, Aguzzi A. Weissmann C, et al. Among authors: aguzzi a. Rev Sci Tech. 1998 Apr;17(1):278-90. doi: 10.20506/rst.17.1.1079. Rev Sci Tech. 1998. PMID: 9638817 Free article. Review.

6

An unusual case of Creutzfeldt-Jakob disease.

Vingerhoets FJ, Hegyi I, Aguzzi A, Myers P, Pizzolato G, Landis T. Vingerhoets FJ, et al. Among authors: aguzzi a. Neurology. 1998 Aug;51(2):617-9. doi: 10.1212/wnl.51.2.617. Neurology. 1998. PMID: 9710052

7

Prion diseases.

Aguzzi A, Weissmann C. Aguzzi A, et al. Haemophilia. 1998 Jul;4(4):619-27. doi: 10.1046/j.1365-2516.1998.440619.x. Haemophilia. 1998. PMID: 9873804 Review.

8

Peripheral pathogenesis of prion diseases.

Glatzel M, Aguzzi A. Glatzel M, et al. Among authors: aguzzi a. Microbes Infect. 2000 May;2(6):613-9. doi: 10.1016/s1286-4579(00)00364-6. Microbes Infect. 2000. PMID: 10884612 Free article. Review.

9

Incidence of Creutzfeldt-Jakob disease in Switzerland.

Glatzel M, Rogivue C, Ghani A, Streffer JR, Amsler L, Aguzzi A. Glatzel M, et al. Among authors: aguzzi a. Lancet. 2002 Jul 13;360(9327):139-41. doi: 10.1016/S0140-6736(02)09384-4. Lancet. 2002. PMID: 12126826

10

Analysis of the prion protein in primates reveals a new polymorphism in codon 226 (Y226F).

Glatzel M, Pekarik V, Lührs T, Dittami J, Aguzzi A. Glatzel M, et al. Among authors: aguzzi a. Biol Chem. 2002 Jun;383(6):1021-5. doi: 10.1515/BC.2002.109. Biol Chem. 2002. PMID: 12222676 Free article.

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