Transient hypoglycorrhachia with paroxysmal abnormal eye movement in early infancy-Reference-Cited by-同舟云学术

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Transient hypoglycorrhachia with paroxysmal abnormal eye movement in early infancy

Published:2021-03 Issue:3 Volume:43 Page:482-485
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Tajima Daisuke,Nakamura Takuji,Ichinose Fumio,Okamoto Nobuhiko,Tomonoh Yuko,Uda Keiko,Furukawa Rie,Tashiro Katsuya,Matsuo Muneaki

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,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. Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan;Ito;Brain Dev,2015

3. Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: a nationwide survey;Fujii;Brain Dev,2016

4. Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?;Klepper;Pediatr Neurol,2003

5. Glut1 deficiency: when to suspect and how to diagnosis;Veroatti;Eur J Pediatr Neurol,2012

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