uric acid has been researched along with Athetoid Movements in 67 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Certain gouty subjects with excessive de novo purine synthesis are deficient in hypoxanthineguanine phosphoribosyltransferase (HG-PRTase [EC 2." | 3.65 | Mechanism of excessive purine biosynthesis in hypoxanthine-guanine phosphoribosyltransferase deficiency. ( Sorensen, LB, 1970) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 67 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| LESCH, M | 2 |
| NYHAN, WL | 5 |
| HOEFNAGEL, D | 2 |
| ANDREW, ED | 1 |
| MIREAULT, NG | 1 |
| BERNDT, WO | 1 |
| Michener, WM | 1 |
| Laplane, R | 1 |
| Polonovski, C | 1 |
| Graveleau, D | 1 |
| Marie, J | 1 |
| Royer, P | 1 |
| Rappaport, R | 1 |
| Gottlieb, RP | 1 |
| Koppel, MM | 1 |
| Bakay, B | 2 |
| Nissinen, E | 1 |
| Borden, M | 1 |
| Page, T | 1 |
| Proctor, P | 1 |
| McGinness, JE | 1 |
| Beardmore, TD | 1 |
| Fox, IH | 2 |
| Kelley, WN | 6 |
| Reed, WB | 2 |
| Fish, CH | 1 |
| Rundle, AT | 1 |
| Fannin, CV | 1 |
| Lenoch, F | 1 |
| Kölle, G | 1 |
| Felix, JS | 1 |
| DeMars, R | 1 |
| Dawson, DM | 1 |
| Rautenstrauch, T | 1 |
| Wyngaarden, JB | 1 |
| McDonald, JA | 1 |
| Wood, MH | 1 |
| Fox, RM | 1 |
| Vincent, L | 1 |
| Reye, C | 1 |
| O'Sullivan, WJ | 1 |
| Emmerson, BT | 2 |
| Crawhall, JC | 1 |
| Henderson, JF | 1 |
| Meigel, W | 1 |
| Braun-Falco, O | 1 |
| Leiber, B | 1 |
| Olbrich, G | 1 |
| Müller, MM | 1 |
| Stemberger, H | 1 |
| Sweetman, L | 1 |
| Wada, Y | 2 |
| Seegmiller, JE | 4 |
| Wallace, DC | 1 |
| Thompson, CJ | 1 |
| Van Heeswijk, PJ | 1 |
| Blank, CH | 1 |
| Jacobson, CB | 1 |
| Greene, ML | 1 |
| Láhoda, F | 1 |
| Ross, A | 1 |
| Manzke, H | 2 |
| Harms, D | 1 |
| Dörner, K | 2 |
| Kastner, C | 1 |
| Berman, PH | 3 |
| Balis, ME | 3 |
| Dancis, J | 3 |
| Kaiser, W | 1 |
| Zöllner, N | 1 |
| Jones, CE | 1 |
| Smith, EE | 1 |
| Hicks, W | 1 |
| Crowell, JW | 1 |
| Sorensen, LB | 2 |
| van der Zee, SP | 2 |
| Lommen, EJ | 1 |
| Trijbels, JM | 1 |
| Schretlen, ED | 2 |
| Ghadimi, H | 1 |
| Bhalla, CK | 1 |
| Kirchenbaum, DM | 1 |
| Choi, KW | 1 |
| Bloom, AD | 1 |
| Boyle, JA | 1 |
| Raivio, KO | 1 |
| Astrin, KH | 1 |
| Schulman, JD | 1 |
| Graf, ML | 1 |
| Jacobsen, CB | 1 |
| Omura, GA | 1 |
| Jolley, RL | 1 |
| Scott, CD | 1 |
| Chow, DC | 1 |
| Kawahara, FS | 1 |
| Saunders, T | 1 |
| Sarto, GE | 1 |
| Dizmang, LH | 1 |
| Cheatham, CF | 1 |
| Newcombe, DS | 3 |
| Arima, M | 1 |
| Aoki, N | 1 |
| Ono, K | 1 |
| Vaisrub, S | 1 |
| Mizuno, T | 1 |
| Segawa, M | 1 |
| Kurumada, T | 1 |
| Maruyama, H | 1 |
| Onisawa, J | 1 |
| Benke, PJ | 1 |
| Krakoff, IH | 1 |
| Dreifuss, FE | 2 |
| Shapiro, SL | 2 |
| Sheppard, GL | 2 |
| Monnens, LA | 1 |
| Byrne, WL | 1 |
5 reviews available for uric acid and Athetoid Movements
| Article | Year |
|---|---|
[Lesh-Nyhan syndrome. Paralysis cerebralis hyperurinogenica].
Topics: Adolescent; Adult; Athetosis; Chemical Phenomena; Chemistry; Child; Compulsive Behavior; Female; Hum | 1970 |
Diagnosis and treatment of the Lesch-Nyhan syndrome.
Topics: Allopurinol; Amniocentesis; Athetosis; Brain; Erythrocytes; Fibroblasts; Humans; Intellectual Disabi | 1972 |
[Congenital disorder of purine metabolism].
Topics: Athetosis; Chorea; Compulsive Behavior; Humans; Intellectual Disability; Metabolism, Inborn Errors; | 1970 |
[Treatment of congenital purine-pyrimidine metabolism anomalies].
Topics: Athetosis; Chorea; Compulsive Behavior; Gout; Humans; Intellectual Disability; Orotic Acid; Purine-P | 1971 |
Biochemical and genetic studies of an X-linked neurological disease (The Lesch-Nyhan syndrome).
Topics: Animals; Athetosis; Cells, Cultured; Cerebral Palsy; Child; Disease Models, Animal; Feedback; Female | 1971 |
1 trial available for uric acid and Athetoid Movements
| Article | Year |
|---|---|
Effects of the uricogenic agent, 2-ethylamino-1,3,4-thiadiazole in hypoxanthine-guanine phosphoribosyl transferase deficiency.
Topics: Adolescent; Athetosis; Azoles; Carbon Isotopes; Cerebral Palsy; Child; Chorea; Clinical Trials as To | 1968 |
61 other studies available for uric acid and Athetoid Movements
| Article | Year |
|---|---|
A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.
Topics: Athetosis; Biomedical Research; Blood Chemical Analysis; Central Nervous System Diseases; Cerebral P | 1964 |
THE SYNDROME OF ATHETOID CEREBRAL PALSY, MENTAL DEFICIENCY, SELF-MUTILATION AND HYPERURICEMIA.
Topics: Athetosis; Blood Chemical Analysis; Blood Urea Nitrogen; Cerebral Palsy; Child; Genetics, Medical; H | 1965 |
HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES.
Topics: Athetosis; Blood; Child; Chorea; Colorimetry; Genetics, Medical; Humans; Hyperuricemia; Infant; Male | 1965 |
Hyperuricemia and mental retardation with athetosis and self-mutilation.
Topics: Allopurinol; Athetosis; Body Height; Body Weight; Child; Child, Preschool; Chorea; Humans; Infant; I | 1967 |
[Congenital hyperuricemia in a cerebro-renal form].
Topics: Athetosis; Child; Humans; Kidney Diseases; Male; Uric Acid | 1967 |
[Congenital hyperuricemia with neurologic, renal and blood disturbances].
Topics: Adolescent; Allopurinol; Anemia, Macrocytic; Athetosis; Chorea; Gout; Humans; Intellectual Disabilit | 1967 |
Hyperuricaemia and choreoathetosis in a child without mental retardation or self-mutilation - a new HPRT variant.
Topics: Adolescent; Athetosis; Chorea; Erythrocytes; Fibroblasts; Humans; Hypoxanthine Phosphoribosyltransfe | 1982 |
Levodopa side-effects and the Lesch-Nyhan syndrome.
Topics: Athetosis; Chorea; Compulsive Behavior; Diagnosis, Differential; Dihydroxyphenylalanine; Humans; Int | 1970 |
Effect of allopurinol on pyrimidine metabolism in the Lesch-Nyhan syndrome.
Topics: Allopurinol; Athetosis; Child; Chorea; Compulsive Behavior; Humans; Intellectual Disability; Orotic | 1970 |
Hyperuricemia with self-mutilation and choreo-athetosis. Lesch-Nyhan syndrome.
Topics: Athetosis; Child; Humans; Huntington Disease; Intellectual Disability; Male; Self Mutilation; Uremia | 1966 |
A survey of serum uric acid levels in mentally retarded patients.
Topics: Adolescent; Adult; Aged; Athetosis; Central Nervous System Diseases; Down Syndrome; Female; Humans; | 1966 |
Studies on the adenine phosphoribosyltransferase enzyme in human fibroblasts lacking hypoxanthine-guanine phosphoribosyltransferase.
Topics: Athetosis; Compulsive Behavior; Culture Techniques; Fibroblasts; Humans; Huntington Disease; Intelle | 1971 |
[Hyperuricemia and gout in childhood (Lesch-Nyhan syndrome)].
Topics: Adolescent; Athetosis; Brain; Child; Child, Preschool; Compulsive Behavior; Gout; Humans; Huntington | 1971 |
Detection of females heterozygous for the Lesch-Nyhan mutation by 8-azaguanine-resistant growth of cultured fibroblasts.
Topics: Athetosis; Autoradiography; Azaguanine; Biopsy; Compulsive Behavior; Culture Techniques; Female; Fib | 1971 |
Absence of guanine deaminase from cerebellum.
Topics: Aminohydrolases; Animals; Athetosis; Brain; Brain Chemistry; Cats; Caudate Nucleus; Cerebellum; Cere | 1971 |
Hyperuricemia. Case presentation.
Topics: Adolescent; Adult; Athetosis; Child; Child, Preschool; Diagnosis, Differential; Fibroblasts; Humans; | 1971 |
[Lesch-Nyhan syndrome].
Topics: Allopurinol; Athetosis; Child; Compulsive Behavior; Diet Therapy; Humans; Huntington Disease; Intell | 1974 |
Regulation of purine biosynthesis in cultured human cells. I. Effects of orotic acid.
Topics: Adolescent; Adult; Athetosis; Cell Line; Chorea; Compulsive Behavior; Culture Techniques; Fibroblast | 1970 |
Lesch-Nyhan syndrome: altered kinetic properties of mutant enzyme.
Topics: Athetosis; Child; Chorea; Compulsive Behavior; Diphosphates; Erythrocytes; Guanine; Humans; Hypoxant | 1971 |
[Genetic aspects in dermatology].
Topics: Adult; Alopecia; Amino Acid Metabolism, Inborn Errors; Athetosis; Carotid Body Tumor; Chorea; Chromo | 1970 |
Activation of variants of hypoxanthine-guanine phosphoribosyl transferase by the normal enzyme.
Topics: Athetosis; Carbon Isotopes; Chromatography, Gel; Diphosphates; Electrophoresis, Disc; Enzyme Activat | 1972 |
The Lesch-Nyhan syndrome: report of three cases.
Topics: Adenine; Adolescent; Adult; Allopurinol; Athetosis; Australia; Child; Humans; Hypoxanthines; Intelle | 1972 |
Metabolic implications of the Lesch-Nyhan syndrome.
Topics: Athetosis; Gout; Humans; Intellectual Disability; Lesch-Nyhan Syndrome; Mass Screening; Purine-Pyrim | 1972 |
[Self mutilation of the lower lip, associated with athetosis and oligophrenia without purine metabolism disorder ("pseudo Lesch-Nyhan syndrome")].
Topics: Athetosis; Clinical Enzyme Tests; Diagnosis, Differential; Guanine; Humans; Hypoxanthines; Infant; I | 1973 |
[Lesch-Nyhan syndrome].
Topics: Aggression; Athetosis; Bites, Human; Chorea; Glycine; Humans; Hyperlipidemias; Intellectual Disabili | 1973 |
[Biochemical and immunological studies of hypoxanthine-guanine phosphoribosyltransferase in erythrocytes of Lesch-Nyhan patients (author's transl)].
Topics: Athetosis; Child; Clinical Enzyme Tests; Compulsive Behavior; Coombs Test; Erythrocytes; Guanine; Hu | 1974 |
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells.
Topics: Adolescent; Adult; Aged; Athetosis; Child; Child, Preschool; Chorea; Compulsive Behavior; Erythrocyt | 1972 |
Preventive control of the Lesch-Nyhan syndrome.
Topics: Abortion, Therapeutic; Amniocentesis; Amniotic Fluid; Athetosis; Chromatography, Thin Layer; Creatin | 1972 |
Clinical features of the Lesch-Nyhan syndrome.
Topics: Adolescent; Allopurinol; Athetosis; Child, Preschool; Humans; Intellectual Disability; Lesch-Nyhan S | 1972 |
Biochemistry of the X-linked uric aciduria--enzyme defect and its genetic variants.
Topics: Athetosis; Gout; Guanine; Humans; Hypoxanthines; Intellectual Disability; Lesch-Nyhan Syndrome; Phos | 1972 |
Clinical features of patients with the "partial" deficiency of the X-linked uricaciduria enzyme.
Topics: Adult; Athetosis; Female; Gout; Humans; Hypoxanthines; Intellectual Disability; Lesch-Nyhan Syndrome | 1972 |
[Neurological complications in uricopathy].
Topics: Adult; Athetosis; Cardiovascular Diseases; Chorea; Compulsive Behavior; Female; Humans; Intellectual | 1972 |
[Treatment of congenital hyperuricemia].
Topics: Adolescent; Allopurinol; Athetosis; Child; Humans; Hypoxanthines; Intellectual Disability; Lesch-Nyh | 1971 |
[Juvenile hyperuricemia, gout and cerebral palsy (Lesch-Nyhan syndrome)].
Topics: Adolescent; Allopurinol; Athetosis; Cerebral Palsy; Chorea; Gout; Humans; Male; Uric Acid | 1969 |
A method for the prenatal diagnosis of the Lesch-Nyhan syndrome using fresh amniotic cells.
Topics: Amniotic Fluid; Athetosis; Chorea; Female; Fetal Diseases; Fetus; Gestational Age; Humans; Intellect | 1969 |
[Lesh-Nyhan syndrome. A congenital defect of purine metabolism with the clinical symptoms of gout and central nervous disorders].
Topics: Athetosis; Child, Preschool; Chorea; Compulsive Behavior; Erythrocytes; Female; Humans; Infant; Inte | 1970 |
Determination of urinary purines in hyperuricosuric children by thin-layer chromatography.
Topics: Allopurinol; Athetosis; Child; Child, Preschool; Chorea; Chromatography, Thin Layer; Densitometry; H | 1970 |
Mechanism of excessive purine biosynthesis in hypoxanthine-guanine phosphoribosyltransferase deficiency.
Topics: Adult; Allopurinol; Athetosis; Carbon Isotopes; Child; Chorea; Compulsive Behavior; Deficiency Disea | 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 |
Biochemically marked lymphocytoid lines: establishment of Lesch-Nyhan cells.
Topics: Athetosis; Cell Line; Chorea; Compulsive Behavior; Culture Techniques; Humans; Hypoxanthines; Immuno | 1970 |
Lesch-Nyhan syndrome: preventive control by prenatal diagnosis.
Topics: Adenine; Amniotic Fluid; Athetosis; Autoradiography; Basal Ganglia; Carbon Isotopes; Cerebellum; Cer | 1970 |
Diagnosis of the Lesch-Nyhan syndrome.
Topics: Athetosis; Chorea; Compulsive Behavior; Humans; Intellectual Disability; Purines; Self Mutilation; T | 1970 |
Preliminary results from high-resolution analyses of ultraviolet-absorbing and carbohydrate constituents in several pathologic body fluids.
Topics: Adolescent; Adult; Alkaptonuria; Allopurinol; Amniotic Fluid; Athetosis; Carbohydrates; Chorea; Chro | 1970 |
A new assay method for hypoxanthine-guanine phosphoribosyltransferase.
Topics: Adenine; Adenine Nucleotides; Athetosis; Carbon Isotopes; Chorea; Chromatography; Compulsive Behavio | 1970 |
Prenatal diagnosis of genetic disorders by amniocentesis.
Topics: Adult; Amniotic Fluid; Athetosis; Chorea; Chromosome Aberrations; Chromosome Disorders; Compulsive B | 1970 |
The Lesch-Nyhan syndrome.
Topics: Adolescent; Aggression; Athetosis; Blood Specimen Collection; Child; Child Development; Chorea; Comp | 1970 |
The urinary excretion of aminoimidazolecarboxamide in the Lesch-Nyhan syndrome.
Topics: Adolescent; Athetosis; Child; Child, Preschool; Chorea; Compulsive Behavior; Female; Folic Acid; Hum | 1970 |
Lesch-Nyhan syndrome.
Topics: Allopurinol; Athetosis; Benzofurans; Brain; Child; Child, Preschool; Chorea; Compulsive Behavior; Er | 1970 |
Lesch-Nyhan syndrome: preventive control.
Topics: Athetosis; Chorea; Compulsive Behavior; Humans; Intellectual Disability; Purine-Pyrimidine Metabolis | 1970 |
Inborn terror of metabolism.
Topics: Athetosis; Chorea; Compulsive Behavior; Female; Humans; Intellectual Disability; Male; Pregnancy; Pu | 1970 |
Clinical and therapeutic aspects of the Lesch-Nyhan syndrome in Japanese children.
Topics: Allopurinol; Athetosis; Azathioprine; Benzofurans; Child; Child, Preschool; Guanine; Humans; Hypoxan | 1970 |
Alteration of purine control mechanisms in patients with the Lesch-Nyhan mutation.
Topics: Athetosis; Chorea; Compulsive Behavior; Diseases in Twins; Female; Humans; Infant, Newborn; Intellec | 1971 |
[Simple determination of purines by preparative thin-layer chromatography].
Topics: Athetosis; Chorea; Chromatography, Thin Layer; Compulsive Behavior; Diagnosis, Differential; Gout; H | 1971 |
Hyperuricosuria and central nervous system dysfunction.
Topics: Athetosis; Child; Child, Preschool; Female; Humans; Hypoxanthines; Lesch-Nyhan Syndrome; Male; Psych | 1967 |
X-linked primary hyperuricaemia (hypoxanthine-guanine phosphoribosyltransferase deficiency encephalopathy.
Topics: Allopurinol; Athetosis; Child; Genes, Recessive; Guanine Nucleotides; Humans; Hypoxanthines; Intelle | 1968 |
[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 |
Molecular approaches to the central nervous system: AAAS Symposium 29-31 December 1968. Dallas, Texas.
Topics: Athetosis; Cerebral Palsy; Chorea; Glucosyltransferases; Humans; Intellectual Disability; Molecular | 1968 |
Congenital hyperuricemia. An inborn error of purine metabolism associated with psychomotor retardation, athetosis, and self-mutilation.
Topics: Adenine; Allopurinol; Athetosis; Child, Preschool; Diet Therapy; Genes, Recessive; Humans; Male; Met | 1969 |
Childhood hyperuricemia with brain disorder.
Topics: Athetosis; Brain Damage, Chronic; Child; Child, Preschool; Humans; Infant; Intellectual Disability; | 1965 |
X-linked recessive inheritance of a syndrome of mental retardation with hyperuricemia.
Topics: Athetosis; Humans; Intellectual Disability; Male; Molecular Biology; Muscle Spasticity; Purine-Pyrim | 1966 |