Literature DB >> 2693620

Temporal evolution of electroencephalographic abnormalities in Creutzfeldt-Jakob disease.

G K Schlenska1, G F Walter.   

Abstract

Frequent serial EEG investigations of three patients with neuropathologically confirmed Creutzfeldt-Jakob disease lasting 13, 24 and 68 weeks revealed typical periodic activity of short duration with stereotyped bilateral sharp waves at the 7th, 8th, and 12th week, respectively, after the onset of symptoms. During the later stages, there were several deviations from this typical pattern. However, periodic activity was preceded between the 3rd and 9th week by intermittent localized or lateralized delta rhythms, which gradually changed into periodic activity. This early temporal evolution of EEG abnormalities may be helpful in the early diagnosis of Creutzfeldt-Jakob disease when accompanied by other investigations to exclude other causes of intermittent delta rhythms.

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Year:  1989        PMID: 2693620     DOI: 10.1007/bf00328506

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  33 in total

1.  [Clinical aspects & neuropathology of subacute presenile spongiform atrophy with dyskinetic terminal stage].

Authors:  H JACOB; W EICKE; H ORTHNER
Journal:  Dtsch Z Nervenheilkd       Date:  1958

2.  Rapidly progressive cerebral degeneration (subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy.

Authors:  D P JONES; S NEVIN
Journal:  J Neurol Neurosurg Psychiatry       Date:  1954-05       Impact factor: 10.154

3.  Creutzfeldt-Jakob disease. An electroencephalographic study.

Authors:  L J Burger; A J Rowan; E S Goldensohn
Journal:  Arch Neurol       Date:  1972-05

4.  Creutzfeldt-Jakob disease. The neuropathology of a transmission experiment.

Authors:  E Beck; P M Daniel; W B Matthews; D L Stevens; M P Alpers; D M Asher; D C Gajdusek; C J Gibbs
Journal:  Brain       Date:  1969       Impact factor: 13.501

5.  The EEG and clinical evolution in Creutzfeldt-Jacob disease.

Authors:  S Erkulwater
Journal:  Clin Electroencephalogr       Date:  1987-10

6.  Subacute spongiform encephalopathy with periodic paroxysmal activities: clinical evolution and serial EEG findings in 20 cases.

Authors:  U Aguglia; G Farnarier; P Tinuper; M Rey; M Gomez; A Quattrone
Journal:  Clin Electroencephalogr       Date:  1987-07

7.  Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery.

Authors:  C Bernoulli; J Siegfried; G Baumgartner; F Regli; T Rabinowicz; D C Gajdusek; C J Gibbs
Journal:  Lancet       Date:  1977-02-26       Impact factor: 79.321

8.  Creutzfeld-Jakob disease: clinical, EEG and neuropathological findings in a cluster of eleven patients.

Authors:  A Lechi; F Tedeschi; D Mancia; V Pietrini; F Tagliavini; M G Terzano; G Trabattoni
Journal:  Ital J Neurol Sci       Date:  1983-04

9.  Electroencephalographic and clinicopathological studies on Creutzfeldt-Jakob syndrome.

Authors:  K Goto; H Umezaki; M Suetsugu
Journal:  J Neurol Neurosurg Psychiatry       Date:  1976-10       Impact factor: 10.154

10.  Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes.

Authors:  J M Bockman; S B Prusiner; J Tateishi; D T Kingsbury
Journal:  Ann Neurol       Date:  1987-06       Impact factor: 10.422

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