Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease With Valine Homozygosity at Codon 129 of the Prion Protein Gene
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| Veröffentlicht in: | JAMA neurology 2014-09, Vol.71 (9), p.1186-1187 |
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| container_end_page | 1187 |
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| container_issue | 9 |
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| container_title | JAMA neurology |
| container_volume | 71 |
| creator | Furukawa, Fumiko Ishibashi, Satoru Sanjo, Nobuo Yamashita, Hiroshi Mizusawa, Hidehiro |
| description | |
| doi_str_mv | 10.1001/jamaneurol.2014.548 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 2168-6149 |
| ispartof | JAMA neurology, 2014-09, Vol.71 (9), p.1186-1187 |
| issn | 2168-6149 2168-6157 |
| language | eng |
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| source | MEDLINE; American Medical Association Journals |
| subjects | Cerebellar Cortex - metabolism Codon - genetics Creutzfeldt-Jakob Syndrome - genetics Creutzfeldt-Jakob Syndrome - metabolism Creutzfeldt-Jakob Syndrome - pathology Creutzfeldt-Jakob Syndrome - physiopathology Diffusion Magnetic Resonance Imaging Electroencephalography Homozygote Humans Male Middle Aged Positron-Emission Tomography Prions - genetics Thalamus - metabolism Thalamus - pathology Valine - genetics |
| title | Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease With Valine Homozygosity at Codon 129 of the Prion Protein Gene |
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