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New Paradigm for the Treatment of Glucose Transporter 1 Deficiency Syndrome: Low Glycemic Index Diet and Modified High Amylopectin Cornstarch

  • Published:2015-09 Issue:3 Volume:53 Page:243-246
  • ISSN:0887-8994
  • Container-title:Pediatric Neurology
  • language:en
  • Short-container-title:Pediatric Neurology

Author:

Almuqbil Mohammed,Go Cristina,Nagy Laura L.,Pai Nisha,Mamak Eva,Mercimek-Mahmutoglu Saadet

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay;De Vivo;N Engl J Med,1991

2. Glucose Transporter Type 1 Deficiency Syndrome;Wang,2002

3. Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome;Klepper;J Clin Lab Anal,1999

4. Glucose transporter 1 deficiency syndrome and other glycolytic defects;De Vivo;J Child Neurol,2002

5. The spectrum of movement disorders in Glut-1 deficiency;Pons;Mov Disord,2010

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