Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
about
GLUT1 deficiency syndrome into adulthood: a follow-up study.Treatable causes of cerebellar ataxia.A novel diagnostic approach to patients with myoclonus.Glucose Transporters at the Blood-Brain Barrier: Function, Regulation and Gateways for Drug Delivery.Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and Epilepsy.Triheptanoin for the treatment of brain energy deficit: A 14-year experience.Gene therapy for a mouse model of glucose transporter-1 deficiency syndrome.Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet.Comparative study of expression and activity of glucose transporters between stem cell-derived brain microvascular endothelial cells and hCMEC/D3 cells.Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome.[Epilepsy-new diagnostic tools, old drugs? : Therapeutic consequences of epilepsy genetics].
P2860
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P2860
Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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name
Cerebrospinal fluid analysis i ...... syndrome: a systematic review.
@en
type
label
Cerebrospinal fluid analysis i ...... syndrome: a systematic review.
@en
prefLabel
Cerebrospinal fluid analysis i ...... syndrome: a systematic review.
@en
P2093
P1433
P1476
Cerebrospinal fluid analysis i ...... syndrome: a systematic review.
@en
P2093
Erik-Jan Kamsteeg
Michèl A Willemsen
Ron A Wevers
Wilhelmina G Leen
P304
P356
10.1001/JAMANEUROL.2013.3090
P407
P577
2013-11-01T00:00:00Z