Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome-Reference-Cited by-同舟云学术

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Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome

Published:2021-02 Issue: Volume: Page:
ISSN:2173-5808
Container-title:Neurología (English Edition)
language:en
Short-container-title:Neurología (English Edition)

Author:

Jiménez Legido M.,Cortés Ledesma C.,Bernardino Cuesta B.,López Marín L.,Cantarín Extremera V.,Pérez-Cerdá C.,Pérez González B.,López Martín E.,González Gutiérrez-Solana L.

Publisher

Elsevier BV

Subject

General Materials Science

Reference20 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 I deficiency (G1D) at 25 (1990–2015): presumptions, facts, and the lives of persons with this rare disease;Pascual;Pediatr Neurol.,2015

3. GLUT1 deficiency syndrome in clinical practice;Klepper;Epilepsy Res.,2012

4. Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder;Leen;Brain.,2010

5. Clinical aspects of glucose transporter type 1 deficiency: information from a global registry;Hao;JAMA Neurol.,2017

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dietary management and access to treatment for patients with glucose deficiency syndrome type 1: an overview review with focus on the European regulatory framework;European Journal of Clinical Nutrition;2024-08-10

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