Le syndrome de déficit en transporteur du glucose de type 1 (GLUT-1)
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference37 articles.
1. Autosomal dominant glut-1 deficiency syndrome and familial epilepsy;Brockmann;Ann Neurol,2001
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 transporter protein deficiency: an emerging syndrome with therapeutic implications;De Vivo;Int Pediatr,1995
4. Glucose transporter 1 deficiency syndrome and other glycolytic defects;De Vivo;J Child Neurol,2002
5. Identification and characterization of the glucose transporter of the blood-brain barrier by cytochalasin B binding and immunological reactivity;Dick;Proc Natl Acad Sci U S A,1984
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1. GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review;Neurogenetics;2024-01-08
2. Variabilidad fenotípica del déficit de GLUT1: ¿cuándo es necesario sospechar?;Revista Chilena de Pediatría;2020-04-22
3. Aminoglucose-functionalized, redox-responsive polymer nanomicelles for overcoming chemoresistance in lung cancer cells;Journal of Nanobiotechnology;2017-11-28
4. Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome;Current Treatment Options in Neurology;2014-03-16
5. GLUT1 deficiency syndrome: An update;Revue Neurologique;2014-02
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