| 000 | 01469 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250517082648.0 | ||
| 264 | 0 | _c20170117 | |
| 008 | 201701s 0 0 eng d | ||
| 022 | _a1872-7131 | ||
| 024 | 7 |
_a10.1016/j.braindev.2016.02.007 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSell, Katharina | |
| 245 | 0 | 0 |
_aVariable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation. _h[electronic resource] |
| 260 |
_bBrain & development _cSep 2016 |
||
| 300 |
_a777-80 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aBrain _xdiagnostic imaging |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aLeukoencephalitis, Acute Hemorrhagic _xdiagnosis |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMolecular Chaperones _xgenetics |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aNuclear Pore Complex Proteins _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 700 | 1 | _aStorch, Katja | |
| 700 | 1 | _aHahn, Gabriele | |
| 700 | 1 | _aLee-Kirsch, Min Ae | |
| 700 | 1 | _aRamantani, Georgia | |
| 700 | 1 | _aJackson, Sandra | |
| 700 | 1 | _aNeilson, Derek | |
| 700 | 1 | _avon der Hagen, Maja | |
| 700 | 1 | _aHehr, Ute | |
| 700 | 1 | _aSmitka, Martin | |
| 773 | 0 |
_tBrain & development _gvol. 38 _gno. 8 _gp. 777-80 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.braindev.2016.02.007 _zAvailable from publisher's website |
| 999 |
_c25777649 _d25777649 |
||