| 000 | 01502 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250517165028.0 | ||
| 264 | 0 | _c20180509 | |
| 008 | 201805s 0 0 eng d | ||
| 022 | _a1532-2130 | ||
| 024 | 7 |
_a10.1016/j.ejpn.2017.07.003 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSinnige, P F | |
| 245 | 0 | 0 |
_aImaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. _h[electronic resource] |
| 260 |
_bEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _cNov 2017 |
||
| 300 |
_a912-920 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAldehyde Dehydrogenase _xgenetics |
| 650 | 0 | 4 |
_aBrain _xdiagnostic imaging |
| 650 | 0 | 4 |
_aCutis Laxa _xdiagnostic imaging |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNeuroimaging _xmethods |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _avan Ravenswaaij-Arts, C M A | |
| 700 | 1 | _aCaruso, P | |
| 700 | 1 | _aLin, A E | |
| 700 | 1 | _aBoon, M | |
| 700 | 1 | _aRahikkala, E | |
| 700 | 1 | _aCallewaert, B | |
| 700 | 1 | _aMeiners, L C | |
| 773 | 0 |
_tEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _gvol. 21 _gno. 6 _gp. 912-920 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejpn.2017.07.003 _zAvailable from publisher's website |
| 999 |
_c27415814 _d27415814 |
||