000			01936 a2200589 4500
005			20250517221706.0
264		0	_c20181030
008			201810s 0 0 eng d
022			_a1872-7131
024	7		_a10.1016/j.braindev.2018.05.008 _2doi
040			_aNLM _beng _cNLM
100	1		_aMarzin, Pauline
245	0	0	_aEarly-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations. _h[electronic resource]
260			_bBrain & development _cOct 2018
300			_a768-774 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Video-Audio Media
650	0	4	_aAdolescent
650	0	4	_aBrain _xphysiopathology
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aEpilepsy _xdiagnosis
650	0	4	_aFemale
650	0	4	_aHemiplegia _xgenetics
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMovement Disorders _xdiagnosis
650	0	4	_aMutation
650	0	4	_aSeizures _xdiagnosis
650	0	4	_aSodium-Potassium-Exchanging ATPase _xgenetics
700	1		_aMignot, Cyril
700	1		_aDorison, Nathalie
700	1		_aDufour, Louis
700	1		_aVille, Dorothée
700	1		_aKaminska, Anna
700	1		_aPanagiotakaki, Eleni
700	1		_aDienpendaele, Anne-Sophie
700	1		_aPenniello, Marie-José
700	1		_aNougues, Marie-Christine
700	1		_aKeren, Boris
700	1		_aDepienne, Christel
700	1		_aNava, Caroline
700	1		_aMilh, Mathieu
700	1		_aVillard, Laurent
700	1		_aRichelme, Christian
700	1		_aRivier, Clotilde
700	1		_aWhalen, Sandra
700	1		_aHeron, Delphine
700	1		_aLesca, Gaëtan
700	1		_aDoummar, Diane
773	0		_tBrain & development _gvol. 40 _gno. 9 _gp. 768-774
856	4	0	_uhttps://doi.org/10.1016/j.braindev.2018.05.008 _zAvailable from publisher's website
999			_c28489747 _d28489747