Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?-Reference-Cited by-同舟云学术

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Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?

Published:2003-10 Issue:4 Volume:29 Page:321-325
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Klepper Jörg,De Vivo Darryl C,Webb David W,Klinge Lars,Voit Thomas

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. Glucose transporter proteins in brain;Vannucci;Glia,1997

2. 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

3. Glucose transport protein deficiency;De Vivo;International Pediatrics,1995

4. Autosomal dominant glut-1 deficiency syndrome and familial epilepsy;Brockmann;Ann Neurol,2001

5. Autosomal dominant transmission of GLUT1 deficiency;Klepper;Hum Mol Genet,2001

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1. Transient hypoglycorrhachia with paroxysmal abnormal eye movement in early infancy;Brain and Development;2021-03

2. SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCİATED WITH GLUT-1 DEFICIENCY SYNDROME;İstanbul Tıp Fakültesi Dergisi;2020-06-30

3. Disorders of Glucose Transport;Inborn Metabolic Diseases;2016

4. No Mutation in the SLC2A3 Gene in Cohorts of GLUT1 Deficiency Syndrome–Like Patients Negative for SLC2A1 and in Patients with AHC Negative for ATP1A3;JIMD Reports;2013

5. Glucide metabolism disorders (excluding glycogen myopathies);Handbook of Clinical Neurology;2013

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