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Num Mark Subjects (1-10 of 10) Year Entries
18 Found
1   Creutzfeldt-Jakob disease -- 2 Related Subjects   2
2 Creutzfeldt-Jakob disease.   6
3 Creutzfeldt-Jakob disease -- Australia. : Report on the CJD settlement offer / Senate Community Affairs References Committee  1997 1
4  

Creutzfeldt-Jakob Disease, Familial -- See Creutzfeldt-Jakob Syndrome


A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
  1
5  

Creutzfeldt-Jakob Disease, New Variant -- See Creutzfeldt-Jakob Syndrome


A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
  1
6 Creutzfeldt-Jakob disease -- Political aspects.   2
7 Creutzfeldt-Jakob disease -- Social aspects.   2
8 Creutzfeldt-Jakob disease -- United States. : Mad cow U.S.A. : could the nightmare happen here? / Sheldon Rampton and John Stauber  1997 1
9  

Creutzfeldt-Jakob Disease, Variant -- See Creutzfeldt-Jakob Syndrome


A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
  1
10  

Creutzfeldt-Jakob Diseases, Familial -- See Creutzfeldt-Jakob Syndrome


A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
  1
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