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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2008-10-9
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pubmed:abstractText |
The E200K mutation of the PRNP (prion protein) gene is the most common cause of familial Creutzfeldt-Jakob disease (fCJD), which has imaging and clinical features that are similar to the sporadic form. The purpose of this study was to conduct a controlled and blinded evaluation of the sensitivity and specificity of MR imaging in this unique population.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1936-959X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1638-43
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pubmed:meshHeading |
pubmed-meshheading:18635614-Aged,
pubmed-meshheading:18635614-Alleles,
pubmed-meshheading:18635614-Atrophy,
pubmed-meshheading:18635614-Brain,
pubmed-meshheading:18635614-Caudate Nucleus,
pubmed-meshheading:18635614-Cerebellum,
pubmed-meshheading:18635614-Cerebral Cortex,
pubmed-meshheading:18635614-Creutzfeldt-Jakob Syndrome,
pubmed-meshheading:18635614-Diffusion Magnetic Resonance Imaging,
pubmed-meshheading:18635614-Dominance, Cerebral,
pubmed-meshheading:18635614-Female,
pubmed-meshheading:18635614-Humans,
pubmed-meshheading:18635614-Image Processing, Computer-Assisted,
pubmed-meshheading:18635614-Magnetic Resonance Imaging,
pubmed-meshheading:18635614-Male,
pubmed-meshheading:18635614-Middle Aged,
pubmed-meshheading:18635614-Mutation,
pubmed-meshheading:18635614-Prions,
pubmed-meshheading:18635614-Putamen,
pubmed-meshheading:18635614-Sensitivity and Specificity,
pubmed-meshheading:18635614-Thalamus
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pubmed:year |
2008
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pubmed:articleTitle |
MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study.
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pubmed:affiliation |
Department of Radiology, Yale University School of Medicine, New Haven, CT 06520- 8043, USA. robert.fulbright@yale.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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