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Literature DB >> 6345459

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

A Lechi, F Tedeschi, D Mancia, V Pietrini, F Tagliavini, M G Terzano, G Trabattoni.

Abstract

10 of 11 Creutzfeld-Jakob disease patients were seen between February 1975 and November 1979. Whilst the clinical and EEG findings were uniform, the neuropathological changes were not: astrogliosis was always diffuse and widespread but the other typical changes (neuronal loss and spongiosis) varied greatly both in degree and location.

Entities: Disease Species

Mesh：

Year: 1983 PMID： 6345459 DOI： 10.1007/bf02043437

Source DB: PubMed Journal: Ital J Neurol Sci ISSN： 0392-0461

48 in total

1. Epidemiology of Creutzfeldt-Jakob disease in England and Wales.

Authors: W B Matthews
Journal: J Neurol Neurosurg Psychiatry Date: 1975-03 Impact factor: 10.154

2. [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

3. A form of subacute encephalopathy of uncertain aetiology.

Authors: S NEVIN; W H McMENEMEY
Journal: Proc R Soc Med Date: 1958-07

4. [Diffuse atrophic degenerative process, predominantly of the thalamus and corpus striatum; variable extrapyramidal and psychic semeiology; subacute evolution with terminal dementia].

Authors: Y POURSINES; J BOUDOURESQUES; J ROGER
Journal: Rev Neurol (Paris) Date: 1953 Impact factor: 2.607

5. 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

6. Creutzfeldt-Jakob disease treated with amantidine. A report of two cases.

Authors: W L Sanders; T L Dunn
Journal: J Neurol Neurosurg Psychiatry Date: 1973-08 Impact factor: 10.154

7. Creutzfeldt-Jakob disease: further similarities with kuru.

Authors: H Adams; E Beck; A M Shenkin
Journal: J Neurol Neurosurg Psychiatry Date: 1974-02 Impact factor: 10.154

8. Status spongiosus in Jakob-Creutzfeldt disease. Electron microscopic study of a cortical biopsy.

Authors: A Bignami; L S Forno
Journal: Brain Date: 1970 Impact factor: 13.501

9. Observations on oligodendrocyte degeneration, the resolution of status spongiosus and remyelination in cuprizone intoxication in mice.

Authors: W F Blakemore
Journal: J Neurocytol Date: 1972-12

10. Cellular sensitization in kuru, Jakob-Creutzfeldt disease and multiple sclerosis: with a note on the biohazards of slow infection work.

Authors: E J Field; B K Shenton
Journal: Acta Neurol Scand Date: 1975-04 Impact factor: 3.209

5 in total

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

1. Epidemiology of Creutzfeldt-Jakob disease in England and Wales.

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

3. A form of subacute encephalopathy of uncertain aetiology.

4. [Diffuse atrophic degenerative process, predominantly of the thalamus and corpus striatum; variable extrapyramidal and psychic semeiology; subacute evolution with terminal dementia].

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

6. Creutzfeldt-Jakob disease treated with amantidine. A report of two cases.

7. Creutzfeldt-Jakob disease: further similarities with kuru.

8. Status spongiosus in Jakob-Creutzfeldt disease. Electron microscopic study of a cortical biopsy.

9. Observations on oligodendrocyte degeneration, the resolution of status spongiosus and remyelination in cuprizone intoxication in mice.

10. Cellular sensitization in kuru, Jakob-Creutzfeldt disease and multiple sclerosis: with a note on the biohazards of slow infection work.

1. Considerations on a group of 13 patients with Creutzfeldt-Jakob disease in the region of Parma (Italy)

2. A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986).

3. Temporal evolution of electroencephalographic abnormalities in Creutzfeldt-Jakob disease.

4. Early MRI findings in Creutzfeldt-Jakob disease.

5. Epidemiologic implications of Creutzfeldt-Jakob disease in a 19 year-old girl.