uric acid has been researched along with Movement Disorders in 18 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
Movement Disorders: Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In contrast, at complete HPRT deficiency, besides overproduction of uric acid neurological problems appear including spasticity, choreoathetosis, mental retardation, and compulsive self-mutilation." | 1.32 | The biochemical basis of the neurobehavioral abnormalities in the Lesch-Nyhan syndrome: a hypothesis. ( Mitev, VI; Neychev, VK, 2004) |
| "Caffeine alone did not produce any significant modification in functional impairment but the co-administration significantly increased the effect of naproxen." | 1.29 | Usefulness of the pain-induced functional impairment model to relate plasma levels of analgesics to their efficacy in rats. ( Hoyo-Vadillo, C; López-Munoz, FJ; Pérez-Urizar, J, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (77.78) | 18.7374 |
| 1990's | 1 (5.56) | 18.2507 |
| 2000's | 1 (5.56) | 29.6817 |
| 2010's | 1 (5.56) | 24.3611 |
| 2020's | 1 (5.56) | 2.80 |
| Authors | Studies |
|---|---|
| Lee, HF | 1 |
| Hsu, CC | 1 |
| Chi, CS | 1 |
| Tsai, CR | 1 |
| Yu, Z | 1 |
| Zhang, S | 1 |
| Wang, D | 1 |
| Fan, M | 1 |
| Gao, F | 1 |
| Sun, W | 1 |
| Li, Z | 1 |
| Li, S | 1 |
| Neychev, VK | 1 |
| Mitev, VI | 1 |
| Howard, RS | 1 |
| Walzak, MP | 1 |
| Hoyo-Vadillo, C | 1 |
| Pérez-Urizar, J | 1 |
| López-Munoz, FJ | 1 |
| van der Zee, SP | 3 |
| Schretlen, ED | 3 |
| Monnens, LA | 2 |
| Watts, RW | 1 |
| McKeran, RO | 1 |
| Brown, E | 1 |
| Andrews, TM | 1 |
| Griffiths, MI | 1 |
| Proctor, P | 1 |
| Barbeau, A | 1 |
| Mars, H | 1 |
| Gillo-Joffroy, L | 1 |
| Storey, B | 1 |
| Refsum, S | 1 |
| Lommen, EJ | 1 |
| Trijbels, JM | 1 |
| Ghadimi, H | 1 |
| Bhalla, CK | 1 |
| Kirchenbaum, DM | 1 |
| Frost, P | 1 |
| Weinstein, GD | 1 |
| Nyhan, WL | 2 |
| Dodge, PR | 1 |
1 review available for uric acid and Movement Disorders
| Article | Year |
|---|---|
The significance of uric acid in the diagnosis and treatment of Parkinson disease: An updated systemic review.
Topics: Age Factors; Biomarkers; Disease Progression; Humans; Hyperuricemia; Movement Disorders; Oxidative S | 2017 |
17 other studies available for uric acid and Movement Disorders
| Article | Year |
|---|---|
Genotype-Phenotype Dissociation in Two Taiwanese Children with Molybdenum Cofactor Deficiency Caused by MOCS2 Mutation.
Topics: Child; Homozygote; Humans; Magnetic Resonance Imaging; Metal Metabolism, Inborn Errors; Movement Dis | 2022 |
The biochemical basis of the neurobehavioral abnormalities in the Lesch-Nyhan syndrome: a hypothesis.
Topics: Animals; Biochemistry; Brain; Humans; Hypoxanthine Phosphoribosyltransferase; Intellectual Disabilit | 2004 |
A new cause for uric acid stones in childhood.
Topics: Child, Preschool; Humans; Intellectual Disability; Kidney Calculi; Male; Movement Disorders; Self Mu | 1967 |
Usefulness of the pain-induced functional impairment model to relate plasma levels of analgesics to their efficacy in rats.
Topics: Analgesics; Animals; Caffeine; Drug Interactions; Female; Movement Disorders; Naproxen; Pain Measure | 1995 |
Megaloblastic anaemia in the Lesch-Nyhan syndrome.
Topics: Adenine; Anemia, Macrocytic; Cerebral Palsy; Child; Humans; Intellectual Disability; Male; Movement | 1968 |
Hyperuricemia. Case presentation.
Topics: Adolescent; Adult; Athetosis; Child; Child, Preschool; Diagnosis, Differential; Fibroblasts; Humans; | 1971 |
Clinical and biochemical studies on treatment of Lesch-Nyhan syndrome.
Topics: Adenine; Allopurinol; Body Weight; Child, Preschool; Chlorpromazine; Creatinine; Exchange Transfusio | 1974 |
Electron-transfer factors in psychosis and dyskinesia.
Topics: Blood Proteins; Bromides; Dihydroxyphenylalanine; Electron Transport; Epinephrine; Humans; Iron; Lip | 1972 |
Adverse clinical side effects of levodopa therapy.
Topics: Antiparkinson Agents; Arrhythmias, Cardiac; Benserazide; Carboxy-Lyases; Dihydroxyphenylalanine; Ede | 1971 |
The Lesch-Nyhan syndrome.
Topics: Child, Preschool; Humans; Infant Nutrition Disorders; Intellectual Disability; Male; Movement Disord | 1969 |
[Inborn hyperuricemia--an anomaly of uric acid metabolism in connection with psychomotor retardation, involuntary movements and self mutilation, Lesch-Nyhan syndrome].
Topics: Adolescent; Adult; Age Factors; Allopurinol; Child; Child, Preschool; Humans; Infant; Infant, Newbor | 1970 |
The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndrome.
Topics: Adenine; Allopurinol; Athetosis; Bone Marrow; Carbon Isotopes; Child; Child, Preschool; Chorea; Comp | 1970 |
The significance of the deficiency state in Lesch-Nyhan disease.
Topics: Allopurinol; Amino Acids; Athetosis; Carbon Isotopes; Child, Preschool; Chorea; Compulsive Behavior; | 1970 |
Diagnosis of Lesch-Nyhan syndrome by direct study of skin specimens.
Topics: Adenine; Adolescent; Adult; Aged; Child; Clinical Enzyme Tests; Erythrocytes; Female; Fibroblasts; G | 1970 |
[A hereditary disorder of purine metabolism with a cerebral affection and megaloblastic anemia (Lesch-Nyhan syndrome)].
Topics: Anemia, Macrocytic; Athetosis; Bone Marrow Examination; Child, Preschool; Humans; Infant; Male; Meta | 1968 |
A disorder of uric acid metabolism and cerebral function in childhood.
Topics: Central Nervous System Diseases; Child; Child, Preschool; Fingers; Humans; Infant; Intellectual Disa | 1965 |
Disordered uric acid metabolism and neurologic abnormalities.
Topics: Blood-Brain Barrier; Cerebral Palsy; Humans; Infant; Intellectual Disability; Male; Movement Disorde | 1966 |