Isolated arteritis of the central nervous system (CNS) is a relatively rare condition. Of the patients treated at our department two presented with characteristic features and eventually the diagnosis of isolated arteritis of the CNS was established. Headaches and relapsing lesions of cerebral nerves were predominant in the clinical picture of the first patient.
View Article and Find Full Text PDFCesk Neurol Neurochir
November 1985
Cesk Neurol Neurochir
March 1983
Histopathological findings in three temporo-spatially linked cases of Creutzfeldt-Jakob disease (CJD) are reported. The patients were males, unrelated and without positive family history. Their mean age at the onset of the disease was 52.
View Article and Find Full Text PDFA peculiar grouping of Creutzfeldt-Jacob disease (CJD) and of other organic presenile dementia (OPD) cases in a small, prevalently rural area in Czechoslovakia to the east of 19 degrees 35' E and to the north of 48 degrees 15' N was studied. Between August, 1972 and November, 1976, three histologically proven CJD cases, bearing no sporadic of familial patterns, were observed. The distance between their dwellings was 13--17 km.
View Article and Find Full Text PDFGroups of volunteers given intramuscularly 5 or 6.5 dex or perorally 6.5 dex newborn mouse icLD50 of the plaquesegregated "14" clone of the Langat E5 virus strain (tick-borne encephalitis comples) were followed for periods of 12 and 24-27 months.
View Article and Find Full Text PDFA total of 22 persons, given a single intramuscular dose of 3.1 times 10(6) newborn mouse ic LD50/ml of the E5"14" virus (stored for 26 months at 4 degrees C in lyophilized state), were subjected to rigorous clinical, clinical-laboratory and virological investigations. Clinical observations and laboratory tests (blood and cerebrospinal fluid cytology and biochemistry) revealed no ill-effects or deviations attributable to the immunization procedure.
View Article and Find Full Text PDFPsychiatr Neurol Med Psychol (Leipz)
April 1968