Familial Creutzfeldt-Jakob disease with extensive degeneration of white matter
- 1 October 1983
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 61 (2), 261-275
- https://doi.org/10.1016/0022-510x(83)90010-2
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Transmissible Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)Archives of Neurology, 1981
- AMYOTROPHIC LATERAL SCLEROSIS AND ITS ASSOCIATION WITH DEMENTIA, PARKINSONISM AND OTHER NEUROLOGICAL DISORDERS: A REVIEWBrain, 1981
- Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matterJournal of Neurology, Neurosurgery & Psychiatry, 1981
- Familial Creutzfeldt-Jakob diseaseJournal of the Neurological Sciences, 1980
- Experimental transmission of human subacute spongiform encephalopathy to small rodentsActa Neuropathologica, 1980
- Guillain—Barré syndrome and Hodgkin's diseaseJournal of the Neurological Sciences, 1980
- Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977Annals of Neurology, 1979
- Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodentsAnnals of Neurology, 1979
- SUBACUTE SPONGIFORM ENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE)Brain, 1978
- Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease.Journal of Neurology, Neurosurgery & Psychiatry, 1977