相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Triheptanoin improves brain energy metabolism in patients with Huntington disease
Isaac Mawusi Adanyeguh et al.
NEUROLOGY (2015)
Dietary triheptanoin rescues oligodendrocyte loss, dysmyelination and motor function in the nur7 mouse model of Canavan disease
Jeremy S. Francis et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2014)
Triheptanoin partially restores level of tricarboxylic acid cycle intermediates in the mouse pilocarpine model of epilepsy
Mussie G. Hadera et al.
JOURNAL OF NEUROCHEMISTRY (2014)
GLUT1 deficiency syndrome: An update
D. Gras et al.
REVUE NEUROLOGIQUE (2014)
Triheptanoin for Glucose Transporter Type I Deficiency (G1D) Modulation of Human Ictogenesis, Cerebral Metabolic Rate, and Cognitive Indices by a Food Supplement
Juan M. Pascual et al.
JAMA NEUROLOGY (2014)
Triheptanoin reduces seizure susceptibility in a syndrome-specific mouse model of generalized epilepsy
Tae Hwan Kim et al.
EPILEPSY RESEARCH (2013)
Heptanoate as a neural fuel: energetic and neurotransmitter precursors in normal and glucose transporter I-deficient (G1D) brain
Isaac Marin-Valencia et al.
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM (2013)
Glut1 Deficiency Syndrome and Novel Ketogenic Diets
Joerg Klepper et al.
JOURNAL OF CHILD NEUROLOGY (2013)
Abnormal response to cortical activation in early stages of Huntington disease
Fanny Mochel et al.
MOVEMENT DISORDERS (2012)
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder
Wilhelmina G. Leen et al.
BRAIN (2010)
The Spectrum of Movement Disorders in Glut-1 Deficiency
Roser Pons et al.
MOVEMENT DISORDERS (2010)
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy
F Mochel et al.
MOLECULAR GENETICS AND METABOLISM (2005)