Page last updated: 2024-10-16

carnitine and Dyskinesia Syndromes

carnitine has been researched along with Dyskinesia Syndromes in 8 studies

Research Excerpts

ExcerptRelevanceReference
"A 9-month-old patient was admitted with encephalopathy and acute loss of acquired motor skills during the course of COVID-19 disease."1.62COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1. ( Ahmadzada, S; Aktuglu-Zeybek, C; Kiykim, E; Yalcinkaya, C; Zubarioglu, T, 2021)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (25.00)18.2507
2000's5 (62.50)29.6817
2010's0 (0.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Zubarioglu, T1
Ahmadzada, S1
Yalcinkaya, C1
Kiykim, E1
Aktuglu-Zeybek, C1
Külkens, S1
Harting, I1
Sauer, S1
Zschocke, J1
Hoffmann, GF1
Gruber, S1
Bodamer, OA1
Kölker, S1
Silva-Adaya, D1
Pérez-De La Cruz, V1
Herrera-Mundo, MN1
Mendoza-Macedo, K1
Villeda-Hernández, J1
Binienda, Z1
Ali, SF1
Santamaría, A1
Samuraki, M1
Komai, K1
Hasegawa, Y1
Kimura, M1
Yamaguchi, S1
Terada, N1
Yamada, M1
Elpeleg, ON1
Ruitenbeek, W1
Jakobs, C1
Barash, V1
De Vivo, DC1
Amir, N1
Prats Viñas, J1
Corral, I1
Martínez Castrillo, JC1
Martínez-Pardo, M1
Gimeno, A1
Goety, CG1
Tanner, CM1
Cohen, JA1
Thelen, JA1
Carroll, VS1
Klawans, HL1
Fariello, RG1

Trials

1 trial available for carnitine and Dyskinesia Syndromes

ArticleYear
L-acetyl-carnitine in Huntington's disease: double-blind placebo controlled crossover study of drug effects on movement disorder and dementia.
    Movement disorders : official journal of the Movement Disorder Society, 1990, Volume: 5, Issue:3

    Topics: Acetylcarnitine; Adult; Aged; Carnitine; Dementia; Double-Blind Method; Female; Humans; Huntington D

1990

Other Studies

7 other studies available for carnitine and Dyskinesia Syndromes

ArticleYear
COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1.
    Journal of pediatric endocrinology & metabolism : JPEM, 2021, Dec-20, Volume: 34, Issue:12

    Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Brain Diseases, Metabolic; Carnitine; C

2021
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency.
    Neurology, 2005, Jun-28, Volume: 64, Issue:12

    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.
    Journal of neurochemistry, 2008, Volume: 105, Issue:3

    Topics: Animals; Antioxidants; Brain; Carnitine; Convulsants; Disease Models, Animal; Dose-Response Relation

2008
A successfully treated adult patient with L-2-hydroxyglutaric aciduria.
    Neurology, 2008, Mar-25, Volume: 70, Issue:13

    Topics: Adult; Age Factors; Alcohol Oxidoreductases; Brain; Brain Diseases, Metabolic; Brain Diseases, Metab

2008
Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome.
    The Journal of pediatrics, 1995, Volume: 126, Issue:1

    Topics: Acidosis, Lactic; Carnitine; Dichloroacetic Acid; Dihydrolipoamide Dehydrogenase; Fibroblasts; Human

1995
[Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
    Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Child, Preschool;

2001
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
    Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Carnitine

2001