| 000 | 01900 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250517044246.0 | ||
| 264 | 0 | _c20160523 | |
| 008 | 201605s 0 0 eng d | ||
| 022 | _a1532-2130 | ||
| 024 | 7 |
_a10.1016/j.ejpn.2015.07.003 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _avan Egmond, Martje E | |
| 245 | 0 | 0 |
_aMyoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment. _h[electronic resource] |
| 260 |
_bEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _cNov 2015 |
||
| 300 |
_a726-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAnticonvulsants _xtherapeutic use |
| 650 | 0 | 4 |
_aAtaxia Telangiectasia _xetiology |
| 650 | 0 | 4 |
_aBrain Diseases _xcomplications |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aCoffin-Lowry Syndrome _xetiology |
| 650 | 0 | 4 | _aEarly Diagnosis |
| 650 | 0 | 4 | _aElectromyography |
| 650 | 0 | 4 |
_aEpilepsies, Myoclonic _xgenetics |
| 650 | 0 | 4 |
_aEpilepsy _xetiology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMovement Disorders _xetiology |
| 650 | 0 | 4 |
_aMyoclonus _xdrug therapy |
| 650 | 0 | 4 |
_aNAV1.1 Voltage-Gated Sodium Channel _xgenetics |
| 650 | 0 | 4 |
_aNervous System Diseases _xcomplications |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aElting, Jan Willem J | |
| 700 | 1 | _aKuiper, Anouk | |
| 700 | 1 | _aZutt, Rodi | |
| 700 | 1 | _aHeineman, Kirsten R | |
| 700 | 1 | _aBrouwer, Oebele F | |
| 700 | 1 | _aSival, Deborah A | |
| 700 | 1 | _aWillemsen, Michel A | |
| 700 | 1 | _aTijssen, Marina A J | |
| 700 | 1 | _ade Koning, Tom J | |
| 773 | 0 |
_tEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _gvol. 19 _gno. 6 _gp. 726-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejpn.2015.07.003 _zAvailable from publisher's website |
| 999 |
_c25129321 _d25129321 |
||