Creutzfeldt-Jakob disease after liver transplantation
✍ Scribed by Dr Alain Créange; Françoise Gray; Pierre Cesaro; Homa Adle-Biassette; Christophe Duvoux; Daniel Cherqui; Jeanne Bell; Piero Parchi; Pierluigi Gambetti; Jean-Denis Degos
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 403 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
✦ Synopsis
modes of inheritance, age at onset, and ethnic origin, the clinical heterogeneity of the disease and its clinicopathological overlap with other hereditary distal myopathies or oculopharyngeal dystrophy with rimmed vacuoles and amyloid deposits (31 suggests that mutations in exons 16 and 17 of this gene should be also searched in families with these disorders.
📜 SIMILAR VOLUMES
I read with interest the report of the American Neurological Association Committee on Health Care Issues in the January 1986 issue of the Annals, which outlines a uniform system of precautions in the handling of contaminated materials from patients with Creutzfeldt-Jakob disease (CJD) 113. However,