Diagnostic problems during late course in Creutzfeldt-Jakob disease [8]

Journal of Neurology

Volumn 250, Issue 5, 2003, Pages 629-630

  Mollenhauer, Brit ^a   Serafin, Siegfried ^b   Zerr, Inga ^a   Steinhoff, Bernhard J ^c   Otto, Markus ^a   Scherer, Michael ^d   Schulz Schaeffer, Walter J ^a   Poser, Sigrid ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b Fachklinik Neuropsychiatrie Klin P   (Germany)

^c Epilepsiezentrum Kork   (Germany)

^d Institut für Radiologie   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN 14 3 3;

AGED; AKINETIC MUTISM; BEHAVIORAL SCIENCE; CASE REPORT; CEREBROSPINAL FLUID ANALYSIS; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DEATH; DIAGNOSTIC ACCURACY; DISEASE COURSE; EARLY DIAGNOSIS; ELECTROENCEPHALOGRAM; FEMALE; HUMAN; LETTER; LUMBAR PUNCTURE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PNEUMONIA; PRIORITY JOURNAL; PSYCHOSOCIAL WITHDRAWAL;

AGED; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS;

EID: 0038578839     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-003-1059-3     Document Type: Letter

References (10)

1. Poser S, Zerr I, Schulz-Schaeffer WJ, Kretzschmar HA, Felgenhauer K. Die Creutzfeldt-Jakob-Krankheit (1997) Eine Sphinx der heutigen Neurobiologie. Dtsch Med Wochenschr 122:1099-1105
2. Steinhoff BJ, Räcker S, Herrendorf G, et al. (1996) Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol 53:162-166
3. Zerr I, Pocchiari M, Collins S, et al. (2000) Analysis of EEG and CSF 14-3-3 proteins as aid to the diagnosis of Creutzfeldt-Jakob disease. Neurology 55:811-815
4. Schröter A, Zerr I, Henkel K, Tschampa HJ, Finkensteadt M, Poser S (2000) Magnetic resonance imaging in the clinical diagnosis of Creutzfeldt-Jakob disease. Arch Neurol 57:1751-1757
5. Zerr I, Bodemer M, Gefeller O, et al. (1998) Detection of 14-3-3 protein in the cerebrospinal fluid support the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol 43:32-40
6. Zerr I, Schulz-Schaeffer WJ, Giese A, et al. (2000) Current clinical diagnosis of Creutzfeldt-Jakob disease: identification of uncommon variants. Ann Neurol 48:323-329
7. Jimi T, Wakayama Y, Shibuya S, et al. (1992) High levels of nervous system specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease. Clin Chim Acta 211:37-46
8. Schaffler L, Karbowski K, Meier C (1983) Langzeit EEG-Verlaufsuntersuchung bei einem Patienten mit Creutzfeldt-Jakobscher Erkrankung. Z EEG-EMG 14:6-11
9. Otto M, Wiltfang J, Cepek L, et al. (2002) Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology; 58:192-197
10. Otto M, Zerr I, Wilfang J, et al. (1999) Laborchemische Verfahren in der Differentialdiagnose der Creutzfeldt-Jakob-Krankheit. Dt Ärztebl 96:3097-3102