The spectrum of movement disorders in Glut-1 deficiency.
about
Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.Paroxysmal eye-head movements in Glut1 deficiency syndromeTreatment of paroxysmal dyskinesias.Glut1 deficiency: inheritance pattern determined by haploinsufficiency.Association between coenzyme Q10 and glucose transporter (GLUT1) deficiency.The use of ketogenic diet in special situations: expanding use in intractable epilepsy and other neurologic disordersParoxysmal Exercise-induced Dyskinesias Caused by GLUT1 Deficiency SyndromeTriheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiencyParoxysmal Nonepileptic Events in Glut1 Deficiency.Dystonic tremor caused by mutation of the glucose transporter gene GLUT1.The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus.Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).Pediatric movement disorders: Five new thingsEpisodic movement disorders: from phenotype to genotype and back.Treatable causes of cerebellar ataxia.Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.Atypical Manifestations in Glut1 Deficiency Syndrome.Triheptanoin for the treatment of brain energy deficit: A 14-year experience.A Cause of Permanent Ketosis: GLUT-1 Deficiency.Glut1 deficiency syndrome and erythrocyte glucose uptake assay.Excellent response to a ketogenic diet in a patient with alternating hemiplegia of childhood.Good outcome in patients with early dietary treatment of GLUT-1 deficiency syndrome: results from a retrospective Norwegian study.Somatic mosaicism for a SLC2A1 mutation: implications for genetic counseling for GLUT1 deficiency syndrome.Analysis of Gait Disturbance in Glut 1 Deficiency Syndrome.Long-Term Effect of GPi-DBS in a Patient With Generalized Dystonia Due to GLUT1 Deficiency Syndrome.Paroxysmal exercise-induced dystonia due to GLUT1 mutation can be responsive to levodopa: a case reportRare and Treatable Cause of Early-Onset Refractory Absence Seizures
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P2860
The spectrum of movement disorders in Glut-1 deficiency.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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name
The spectrum of movement disorders in Glut-1 deficiency.
@en
The spectrum of movement disorders in Glut-1 deficiency.
@nl
type
label
The spectrum of movement disorders in Glut-1 deficiency.
@en
The spectrum of movement disorders in Glut-1 deficiency.
@nl
prefLabel
The spectrum of movement disorders in Glut-1 deficiency.
@en
The spectrum of movement disorders in Glut-1 deficiency.
@nl
P2093
P2860
P356
P1433
P1476
The spectrum of movement disorders in Glut-1 deficiency.
@en
P2093
Abbie Collins
Darryl C De Vivo
Kristin Engelstad
Michael Rotstein
Roser Pons
P2860
P304
P356
10.1002/MDS.22808
P407
P577
2010-02-01T00:00:00Z