carnitine has been researched along with Dyskinesia Syndromes in 8 studies
Excerpt | Relevance | Reference |
---|---|---|
"A 9-month-old patient was admitted with encephalopathy and acute loss of acquired motor skills during the course of COVID-19 disease." | 1.62 | COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1. ( Ahmadzada, S; Aktuglu-Zeybek, C; Kiykim, E; Yalcinkaya, C; Zubarioglu, T, 2021) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (25.00) | 18.2507 |
2000's | 5 (62.50) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Zubarioglu, T | 1 |
Ahmadzada, S | 1 |
Yalcinkaya, C | 1 |
Kiykim, E | 1 |
Aktuglu-Zeybek, C | 1 |
Külkens, S | 1 |
Harting, I | 1 |
Sauer, S | 1 |
Zschocke, J | 1 |
Hoffmann, GF | 1 |
Gruber, S | 1 |
Bodamer, OA | 1 |
Kölker, S | 1 |
Silva-Adaya, D | 1 |
Pérez-De La Cruz, V | 1 |
Herrera-Mundo, MN | 1 |
Mendoza-Macedo, K | 1 |
Villeda-Hernández, J | 1 |
Binienda, Z | 1 |
Ali, SF | 1 |
Santamaría, A | 1 |
Samuraki, M | 1 |
Komai, K | 1 |
Hasegawa, Y | 1 |
Kimura, M | 1 |
Yamaguchi, S | 1 |
Terada, N | 1 |
Yamada, M | 1 |
Elpeleg, ON | 1 |
Ruitenbeek, W | 1 |
Jakobs, C | 1 |
Barash, V | 1 |
De Vivo, DC | 1 |
Amir, N | 1 |
Prats Viñas, J | 1 |
Corral, I | 1 |
Martínez Castrillo, JC | 1 |
Martínez-Pardo, M | 1 |
Gimeno, A | 1 |
Goety, CG | 1 |
Tanner, CM | 1 |
Cohen, JA | 1 |
Thelen, JA | 1 |
Carroll, VS | 1 |
Klawans, HL | 1 |
Fariello, RG | 1 |
1 trial available for carnitine and Dyskinesia Syndromes
Article | Year |
---|---|
L-acetyl-carnitine in Huntington's disease: double-blind placebo controlled crossover study of drug effects on movement disorder and dementia.
Topics: Acetylcarnitine; Adult; Aged; Carnitine; Dementia; Double-Blind Method; Female; Humans; Huntington D | 1990 |
7 other studies available for carnitine and Dyskinesia Syndromes
Article | Year |
---|---|
COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Brain Diseases, Metabolic; Carnitine; C | 2021 |
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency.
Topics: Age of Onset; Aged; Atrophy; Brain Diseases, Metabolic, Inborn; Carnitine; Cerebral Cortex; Cognitio | 2005 |
Excitotoxic damage, disrupted energy metabolism, and oxidative stress in the rat brain: antioxidant and neuroprotective effects of L-carnitine.
Topics: Animals; Antioxidants; Brain; Carnitine; Convulsants; Disease Models, Animal; Dose-Response Relation | 2008 |
A successfully treated adult patient with L-2-hydroxyglutaric aciduria.
Topics: Adult; Age Factors; Alcohol Oxidoreductases; Brain; Brain Diseases, Metabolic; Brain Diseases, Metab | 2008 |
Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome.
Topics: Acidosis, Lactic; Carnitine; Dichloroacetic Acid; Dihydrolipoamide Dehydrogenase; Fibroblasts; Human | 1995 |
[Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Child, Preschool; | 2001 |
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Carnitine | 2001 |