THE CLASSICAL PHENOTYPE OF GLUCOSE TRANSPORTER-1 DEFICIENCY SYNDROME (GLUT-1 DS): DIFFERENT CLINICAL EXPRESSION AND KETOGENIC DIET RESULTS OF PEDIATRIC PATIENTS

被引：0
|
作者：
Bayram, A. Kacar [1 ]
Per, H. [2 ]
Kardas, F. [3 ]
Canpolat, M. [2 ]
Caglayan, A. O. [4 ,5 ,6 ]
Kumandas, S. [2 ]
Kendirci, M. [3 ]
Gumus, H. [2 ]
机构：
[1] Erciyes Univ, Sch Med, Dept Pediat, Div Pediat Neurol, Kayseri, Turkey
[2] Erciyes Univ, Fac Med, Dept Pediat, Div Pediat Neurol, Kayseri, Turkey
[3] Erciyes Univ, Fac Med, Dept Pediat, Div Pediat Nutr & Metab, Kayseri, Turkey
[4] Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT USA
[5] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT USA
[6] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
来源：
EPILEPSIA | 2015年 / 56卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
p0329
引用
收藏
页码：87 / 87
页数：1
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