Page last updated: 2024-08-25

triheptanoin and Carbohydrate Metabolism, Inborn Error

triheptanoin has been researched along with Carbohydrate Metabolism, Inborn Error in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	4 (66.67)	24.3611
2020's	2 (33.33)	2.80

Authors

Authors	Studies
Auvin, S; Blair, S; Brandabur, M; Collins, A; Davis, R; De Vivo, D; Garcia-Cazorla, A; Horvath, R; Kay Koenig, M; Koutsoukos, T; Lacy, A; Miller, I; Saneto, RP; Scheffer, IE; Striano, P; Tzadok, M	1
De Vivo, DC; Monani, UR; Park, SH; Tang, M	1
Atencio, M; Barbier, M; Billette de Villemeur, T; De Saint Martin, A; Gras, D; Hainque, E; Luton, MP; Meneret, A; Mochel, F; Ottolenghi, C; Roze, E	1
Atencio, M; Barbier, M; Doulazmi, M; Gras, D; Habarou, F; Hainque, E; Luton, MP; Meneret, A; Mochel, F; Ottolenghi, C; Roze, E	1
Billette de Villemeur, T; Caillet, S; Doummar, D; Gras, D; Méneret, A; Mochel, F; Roze, E; Vidailhet, M	1
Good, LB; Hernandez, A; Hynan, LS; Kelly, DI; Liu, P; Lu, H; Ma, Q; Mao, D; Marin-Valencia, I; Park, JY; Pascual, JM; Roe, CR; Sheng, M; Stavinoha, P; Zhang, X	1

Reviews

2 review(s) available for triheptanoin and Carbohydrate Metabolism, Inborn Error

Article	Year
Therapeutic strategies for glucose transporter 1 deficiency syndrome. Annals of clinical and translational neurology, 2019, Volume: 6, Issue:9 Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Diet, Ketogenic; Genetic Therapy; Glucose Transporter Type 1; Humans; Monosaccharide Transport Proteins; Mutation; Triglycerides	2019
GLUT1 deficiency syndrome: an update. Revue neurologique, 2014, Volume: 170, Issue:2 Topics: Carbohydrate Metabolism, Inborn Errors; Diet, Ketogenic; Glucose Transporter Type 1; Humans; Monosaccharide Transport Proteins; Phenotype; Thioctic Acid; Triglycerides	2014

Trials

2 trial(s) available for triheptanoin and Carbohydrate Metabolism, Inborn Error

Article	Year
A randomized, double-blind trial of triheptanoin for drug-resistant epilepsy in glucose transporter 1 deficiency syndrome. Epilepsia, 2022, Volume: 63, Issue:7 Topics: Adolescent; Adult; Anticonvulsants; Carbohydrate Metabolism, Inborn Errors; Child; Double-Blind Method; Drug Resistant Epilepsy; Drug Therapy, Combination; Epilepsy, Absence; Glucose Transporter Type 1; Humans; Monosaccharide Transport Proteins; Seizures; Treatment Outcome; Triglycerides	2022
Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect. Journal of neurology, neurosurgery, and psychiatry, 2019, Volume: 90, Issue:11 Topics: Carbohydrate Metabolism, Inborn Errors; Follow-Up Studies; Humans; Monosaccharide Transport Proteins; Triglycerides	2019

Article

Year

A randomized, double-blind trial of triheptanoin for drug-resistant epilepsy in glucose transporter 1 deficiency syndrome.

Epilepsia, 2022, Volume: 63, Issue:7

Topics: Adolescent; Adult; Anticonvulsants; Carbohydrate Metabolism, Inborn Errors; Child; Double-Blind Method; Drug Resistant Epilepsy; Drug Therapy, Combination; Epilepsy, Absence; Glucose Transporter Type 1; Humans; Monosaccharide Transport Proteins; Seizures; Treatment Outcome; Triglycerides

2022

Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect.

Journal of neurology, neurosurgery, and psychiatry, 2019, Volume: 90, Issue:11

Topics: Carbohydrate Metabolism, Inborn Errors; Follow-Up Studies; Humans; Monosaccharide Transport Proteins; Triglycerides

2019

Other Studies

2 other study(ies) available for triheptanoin and Carbohydrate Metabolism, Inborn Error

Article	Year
Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome. Journal of neurology, neurosurgery, and psychiatry, 2020, Volume: 91, Issue:4 Topics: Adolescent; Adult; Ataxia; Carbohydrate Metabolism, Inborn Errors; Confusion; Diet, Ketogenic; Dysarthria; Dystonia; Fatigue; Female; Humans; Male; Monosaccharide Transport Proteins; Triglycerides; Young Adult	2020
Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplement. JAMA neurology, 2014, Volume: 71, Issue:10 Topics: Adolescent; Adult; Blood Glucose; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Citric Acid Cycle; Cohort Studies; Dietary Supplements; Electroencephalography; Female; Glucose; Humans; Magnetic Resonance Imaging; Male; Monosaccharide Transport Proteins; Treatment Outcome; Triglycerides; Young Adult	2014

Article

Year

Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome.

Journal of neurology, neurosurgery, and psychiatry, 2020, Volume: 91, Issue:4

Topics: Adolescent; Adult; Ataxia; Carbohydrate Metabolism, Inborn Errors; Confusion; Diet, Ketogenic; Dysarthria; Dystonia; Fatigue; Female; Humans; Male; Monosaccharide Transport Proteins; Triglycerides; Young Adult

2020

Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplement.

JAMA neurology, 2014, Volume: 71, Issue:10

Topics: Adolescent; Adult; Blood Glucose; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Citric Acid Cycle; Cohort Studies; Dietary Supplements; Electroencephalography; Female; Glucose; Humans; Magnetic Resonance Imaging; Male; Monosaccharide Transport Proteins; Treatment Outcome; Triglycerides; Young Adult

2014