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Page last updated: 2024-08-17

lysine and Movement Disorders

lysine has been researched along with Movement Disorders in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19903 (50.00)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hasegawa, Y; Kimura, M; Komai, K; Samuraki, M; Terada, N; Yamada, M; Yamaguchi, S1
Emons, D; Haverkamp, F; Kreft, B; Woelfle, J1
Prats Viñas, J1
Kyllerman, M; Steen, G1
Fluharty, AL; Kihara, H; Porter, MT; Valente, M1
Bicknell, J; Cavanagh, NP; Howard, F1

Other Studies

6 other study(ies) available for lysine and Movement Disorders

ArticleYear
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, Metabolic, Inborn; Carnitine; Chromosomes, Human, Pair 14; Female; Flavin-Adenine Dinucleotide; Genetic Markers; Genetic Predisposition to Disease; Homozygote; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Movement Disorders; Treatment Outcome

2008
Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall.
    Pediatric radiology, 1996, Volume: 26, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Cisterna Magna; Developmental Disabilities; Diagnosis, Differential; Female; Frontal Lobe; Glutarates; Glutaryl-CoA Dehydrogenase; Hematoma, Subdural; Humans; Infant; Lysine; Magnetic Resonance Imaging; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Psychomotor Performance; Temporal Lobe; Tomography, X-Ray Computed; Tryptophan

1996
[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; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Lysine; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Tryptophan

2001
Intermittently progressive dyskinetic syndrome in glutaric aciduria.
    Neuropadiatrie, 1977, Volume: 8, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Child; Child, Preschool; Female; Glutarates; Humans; Infant; Infant, Newborn; Language Disorders; Lysine; Movement Disorders; Rabbits; Tryptophan

1977
Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines.
    Pediatrics, 1973, Volume: 51, Issue:2

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Antipsychotic Agents; Arginine; Chlorpromazine; Cystinuria; Female; Fluphenazine; Humans; Intellectual Disability; Intestinal Absorption; Kidney Tubules; Lysine; Movement Disorders; Ornithine; Pedigree; Renal Aminoacidurias; Thioridazine; Trihexyphenidyl

1973
Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers.
    Archives of disease in childhood, 1974, Volume: 49, Issue:8

    Topics: Arginine; Child; Cystinuria; Humans; Intellectual Disability; Lysine; Male; Movement Disorders; Ornithine

1974