Creutzfeldt-Jakob disease, a sphinx of current neurobiology;Die Creutzfeldt-Jakob-Krankheit. Eine Sphinx der heutigen Neurobiologie

Deutsche Medizinische Wochenschrift

Volumn 122, Issue 37, 1997, Pages 1099-1105

  Poser, S ^a   Zerr, I ^a   Schulz Schaeffer, W J ^a   Kretzschmar, H A ^a   Felgenhauer, K ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ENOLASE;

ARTICLE; BRAIN SPONGIOSIS; CEREBROSPINAL FLUID; CREUTZFELDT JAKOB DISEASE; DEMENTIA; EUROPE; GERMANY; HISTOLOGY; HUMAN; MAJOR CLINICAL STUDY; NEUROBIOLOGY; PATIENT MONITORING; RISK FACTOR; UNITED KINGDOM;

EID: 0030870357     PISSN: 00120472     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1047733     Document Type: Article

References (23)

1. Aguzzi, A., S. Brandner, M. Klein, T. Blättler: Molekulare Pathogenese der spongiformen Enzephalopathien. Schweiz. Arch. Neurol. Psychiat. 147 (1996), 133-140.
2. Brown, P.: Environmental causes of human spongiform encephalopathy. In Baker, H. F., R. M. Ridley (Ed.): Prion Diseases (Humana Press: Totowa 1996), 139-154.
3. Brown, P., C. J. J. Gibbs, P. Rodgers-Johnson, D. M. Asher, M. P. Sulima, A. Bacote, L. G. Goldfarb, D. C. Gajdusek: Human spongiform encephalopathy. The National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann. Neurol. 35 (1994), 513-529.
4. Budka, H., A. Aguzzi, P. Brown, J. M. Brucher, O. Bugiani, J. Collinge, H. Diringer, F. Gulotta, M. Haltia, J. J. Hauw, J. W. Ironside, H. A. Kretschmar, P. L. Lautos, C. Masullo, M. Pocchiori, W. Schlote, J. Tateishi, R. G. Will: Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol. 5 (1995), 319-322.
5. Finkenstaedt, M., A. Szudra, I. Zerr, S. Poser, J. H. Hise, J. M. Stoebner, T. Weber: MR imaging of Creutzfeldt-Jakob disease. Radiology 199 (1996), 793-798.
6. Hainfellner, J. A., K. Jellinger, H. Diringer, M. Guentchev, R. Kleinert, P. Pilz, H. Maier, H. Budka: Creutzfeldt-Jakob disease in Austria. J. Neurol. Neurosurg. Psychiat. 61 (1996), 139-142.
7. Harrington, M. G., C. R. Merril, D. M. Asher, D. C. Gajdusek: Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. New Engl. J. Med. 315 (1986), 279-283.
8. Hill, A., M. Zeidler, J. Ironside, J. Collinge: Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. Lancet 349 (1997), 99-100.
9. Hsich, G., K. Kenney, C. J. Gibbs, K. H. Lee, M. G. Harrington: The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. New Engl. J. Med. 335 (1996), 924-930.
10. Kretzschmar, H. A., J. W. Ironside, S. J. DeArmond, J. Tateishi: Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch. Neurol. 53 (1996), 913-920.
11. Laporte, R. E.: Assessing the human condition. Capture-recapture techniques. Brit. Med. J. 308 (1994), 5-6.
12. Otto, M., H. Stein, A. Szudra, T. Zerr, M. Bodemer, H. A. Kretzschmar, W. Mäder, S. Poser, T. Weber: Elevated level of S100 protein concentration in CSF of patients with Creutzfeldt-Jakob disease. Akt. Neurol. 23 (1996), 71.
13. Prusiner, S. B.: Prionen-Erkrankungen. Spektr. d. Wiss. (1995), 44-52.
14. Steinhoff, B. J., S. Räcker, G. Herrendorf, S. Poser, S. Grosche, I. Zerr, H. Kretzschmar, T. Weber: Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch. Neurol. 53 (1996), 162-166.
15. van Domburg, P. H., H. J. ten Donkelaar, S. L. Notermanns: Akinetic mutism with bithalamic infarction. Neurophysiological correlates. J. Neurol. Sci. 139 (1996), 58-65.
16. Wakayama, Y., S. Shibuya, J. Kawase, F. Sagawa, Y. Hashizume: High neuron-specific enolase level of cerebrospinal fluid in the early stage of Creutzfeldt-Jakob disease. Klin. Wschr. 65 (1987), 798-801.
17. Wieland, S., F. von Weizäcker, H. E. Blum: Prionen. Dtsch. Med. Wschr. 121 (1996), 949-952.
18. Will, R. G., R. S. G. Knight, M. Zeidler, S., G. Stewart, J. W. Ironside, S. N. Cousens, P. G. Smith: Reporting of suspect new variant Creutzfeldt-Jakob disease. Lancet 349 (1997), 847.
19. Will, R. G., W. B. Matthews: A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I. Clinical features. J. Neurol. Neurosurg. Psychiat. 47 (1984), 134-140.
20. Windl, O., M. Dempster, J. P. Estibeiro, R. Lathe, R. de Silva, T. Esmonde, R. Will, A. Springbett, T. A. Campbell, K. C. Sidle, M. S. Palmer, J. Collinge: Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom. A systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Hum. Genet. 98 (1996), 259-264.
21. Zerr, I., M. Bodemer, M. Otto, S. Poser, O. Windl, H. A. Kretzschmar, O. Gefeller, T. Weber: Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid. Lancet 348 (1996), 846-849.
22. Zerr, I., M. Bodemer, S. Räcker, S. Grosche, S. Poser, H. A. Kretzschmar, T. Weber: Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease. Lancet 345 (1995), 1609-1610.
23. Zerr, I., M. Bodemer, T. Weber: The 14-3-3 brain protein and transmissible spongiform encephalopathy. New Engl. J. Med. 336 (1997), 874.