A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. (Record no. 22228861)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01366 a2200421 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250516120441.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 201301s 0 0 eng d |
| 022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
| International Standard Serial Number | 1526-632X |
| 024 7# - OTHER STANDARD IDENTIFIER | |
| Standard number or code | 10.1212/WNL.0b013e3182749edc |
| Source of number or code | doi |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | NLM |
| Language of cataloging | eng |
| Transcribing agency | NLM |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Ghezzi, Laura |
| 264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | 20130116 |
| 245 00 - TITLE STATEMENT | |
| Title | A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. |
| Medium | [electronic resource] |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Name of publisher, distributor, etc. | Neurology |
| Date of publication, distribution, etc. | Nov 2012 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 2077-8 p. |
| Other physical details | digital |
| 500 ## - GENERAL NOTE | |
| General note | Publication Type: Case Reports; Journal Article |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Aged |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Alanine |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Eukaryotic Initiation Factor-2B |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Female |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Humans |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Leukoencephalopathies |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Mutation |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Valine |
| General subdivision | genetics |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Scarpini, Elio |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Rango, Mario |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Arighi, Andrea |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bassi, Maria Teresa |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Tenderini, Erika |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | De Riz, Milena |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Jacini, Francesca |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Fumagalli, Giorgio G |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Pietroboni, Anna M |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Galimberti, Daniela |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bresolin, Nereo |
| 773 0# - HOST ITEM ENTRY | |
| Title | Neurology |
| Related parts | vol. 79 |
| -- | no. 20 |
| -- | p. 2077-8 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://doi.org/10.1212/WNL.0b013e3182749edc">https://doi.org/10.1212/WNL.0b013e3182749edc</a> |
| Public note | Available from publisher's website |
No items available.