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Volumn 47, Issue 2, 2012, Pages 123-124

The Hitchhiker's guide to the role of (Transient) hypoglycemia in refractory seizures and epilepsy

Author keywords

[No Author keywords available]

Indexed keywords

ACICLOVIR; ANTIBIOTIC AGENT; GLUCOSE; GLUCOSE TRANSPORTER 1;

EID: 84863327492     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2012.04.020     Document Type: Article
Times cited : (4)

References (6)
  • 1
    • 84863320906 scopus 로고    scopus 로고
    • Intractable absence seizures in hyperinsulinsim-hyperammonaemia syndrome
    • this issue
    • K. Nakano, K. Kobayashi, Y. Okano, K. Aso, and Y. Ohtsuka Intractable absence seizures in hyperinsulinsim-hyperammonaemia syndrome Pediatr Neurol 2012 this issue
    • (2012) Pediatr Neurol
    • Nakano, K.1    Kobayashi, K.2    Okano, Y.3    Aso, K.4    Ohtsuka, Y.5
  • 2
    • 79952294449 scopus 로고    scopus 로고
    • Nesidioblastosis no longer! It's all about genetics
    • A.A. Palladino, and C.A. Stnaley Nesidioblastosis no longer! It's all about genetics J Clin Endocrinol Metab 96 2011 617 619
    • (2011) J Clin Endocrinol Metab , vol.96 , pp. 617-619
    • Palladino, A.A.1    Stnaley, C.A.2
  • 3
    • 84858120198 scopus 로고    scopus 로고
    • GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
    • P. Striano, Y.G. Weber, and M.R. Toliat GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy Neurology 78 2012 557 562
    • (2012) Neurology , vol.78 , pp. 557-562
    • Striano, P.1    Weber, Y.G.2    Toliat, M.R.3
  • 4
    • 84858143942 scopus 로고    scopus 로고
    • GLUT1 deficiency: A glut of epilepsy phenotypes
    • I.E. Scheffer GLUT1 deficiency: A glut of epilepsy phenotypes Neurology 78 2012 524 525
    • (2012) Neurology , vol.78 , pp. 524-525
    • Scheffer, I.E.1
  • 5
    • 65549145036 scopus 로고    scopus 로고
    • Eyelid myoclonia with absences (Jeavons syndrome): A well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?
    • S. Striano, G. Capovilla, and V. Sofia Eyelid myoclonia with absences (Jeavons syndrome): A well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions? Epilepsia 50 Suppl. 5 2009 15 19
    • (2009) Epilepsia , vol.50 , Issue.SUPPL. 5 , pp. 15-19
    • Striano, S.1    Capovilla, G.2    Sofia, V.3
  • 6
    • 84857297136 scopus 로고    scopus 로고
    • Eyelid myoclonia with absence seizures in a child with l-2 hydroxyglutaric aciduria: Findings of magnetic resonance imaging
    • A. Mete, S. Isikay, A. Sirikci, A. Ozkur, and M. Bayram Eyelid myoclonia with absence seizures in a child with l-2 hydroxyglutaric aciduria: Findings of magnetic resonance imaging Pediatr Neurol 46 2012 195 197
    • (2012) Pediatr Neurol , vol.46 , pp. 195-197
    • Mete, A.1    Isikay, S.2    Sirikci, A.3    Ozkur, A.4    Bayram, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.