000 01320 a2200373 4500
005 20250516214924.0
264 0 _c20150526
008 201505s 0 0 eng d
022 _a1439-1899
024 7 _a10.1055/s-0034-1378130
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRagona, Francesca
245 0 0 _aRefractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review.
_h[electronic resource]
260 _bNeuropediatrics
_cOct 2014
300 _a328-32 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aCarbohydrate Metabolism, Inborn Errors
_xcomplications
650 0 4 _aChild
650 0 4 _aElectroencephalography
650 0 4 _aEpilepsy, Absence
_xcomplications
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMonosaccharide Transport Proteins
_xdeficiency
650 0 4 _aMutation
_xgenetics
650 0 4 _aSodium-Potassium-Chloride Symporters
_xgenetics
700 1 _aMatricardi, Sara
700 1 _aCastellotti, Barbara
700 1 _aPatrini, Mara
700 1 _aFreri, Elena
700 1 _aBinelli, Simona
700 1 _aGranata, Tiziana
773 0 _tNeuropediatrics
_gvol. 45
_gno. 5
_gp. 328-32
856 4 0 _uhttps://doi.org/10.1055/s-0034-1378130
_zAvailable from publisher's website
999 _c23883965
_d23883965