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Competing interests: FM holds a patent on the use of triheptanoin in GLUT1-DS (WO2014093901).
Figures
Figure 1
(A) Flow chart. (B) Normalised…
Figure 1
(A) Flow chart. (B) Normalised number of paroxysmal events in patients with glucose…
Figure 1
(A) Flow chart. (B) Normalised number of paroxysmal events in patients with glucose transporter type 1 deficiency syndrome (GLUT1-DS) during the different phases of the study. Total and motor numbers of paroxysmal events are expressed in mean per month. Error bars represent SEM. *P<0.05 (Dunn’s tests). m, number of months; n, number of patients.
De Vivo DC, Trifiletti RR, Jacobson RI, et al. . Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay. N Engl J Med 1991;325:703–9. 10.1056/NEJM199109053251006
-
DOI
-
PubMed
Leen WG, Klepper J, Verbeek MM, et al. . Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. Brain 2010;133:655–70. 10.1093/brain/awp336
-
DOI
-
PubMed
Alter AS, Engelstad K, Hinton VJ, et al. . Long-term clinical course of GLUT1 deficiency syndrome. J Child Neurol 2015;30:160–9. 10.1177/0883073814531822
-
DOI
-
PubMed
Pons R, Collins A, Rotstein M, et al. . The spectrum of movement disorders in GLUT-1 deficiency. Mov Disord 2010;25:275–81. 10.1002/mds.22808
-
DOI
-
PubMed
Klepper J, Leiendecker B. GLUT1 deficiency syndrome and novel ketogenic diets. J Child Neurol 2013;28:1045–8. 10.1177/0883073813487600
-
DOI
-
PubMed