glycine has been researched along with Chorea in 9 studies
Chorea: Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES.
| 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) |
| "Because of clinical similarities, benign hereditary chorea and myoclonus-dystonia (DYT11) might be confused." | 1.34 | Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia. ( Asmus, F; Chinnery, PF; Devlin, A; Gasser, T; Munz, M; Zimprich, A, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (77.78) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Asmus, F | 1 |
| Devlin, A | 1 |
| Munz, M | 1 |
| Zimprich, A | 1 |
| Gasser, T | 1 |
| Chinnery, PF | 1 |
| Koh, YH | 1 |
| Lim, WS | 1 |
| Sitoh, YY | 1 |
| McKenzie, GM | 1 |
| Viik, K | 1 |
| McGeer, PL | 1 |
| McGeer, EG | 1 |
| Leiber, B | 1 |
| Olbrich, G | 1 |
| Nyhan, WL | 1 |
| Sweetman, L | 1 |
| Lesch, M | 1 |
| Sorensen, LB | 1 |
| van der Zee, SP | 1 |
| Lommen, EJ | 1 |
| Trijbels, JM | 1 |
| Schretlen, ED | 1 |
| Ghadimi, H | 1 |
| Bhalla, CK | 1 |
| Kirchenbaum, DM | 1 |
1 review available for glycine and Chorea
| Article | Year |
|---|---|
Neurotransmitter synthetic enzymes.
Topics: Acetylcholine; Acetyltransferases; Adenylyl Cyclases; Aging; Aminobutyrates; Animals; Brain; Brain C | 1973 |
1 trial available for glycine and Chorea
| 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 |
7 other studies available for glycine and Chorea
| Article | Year |
|---|---|
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
Topics: Adolescent; Arginine; Child; Chorea; DNA Mutational Analysis; Dystonic Disorders; Exons; Family Heal | 2007 |
An unusual case of nonketotic hyperglycemia presenting as hemichorea.
Topics: Aged; Amino Acid Metabolism, Inborn Errors; Caudate Nucleus; Chorea; Diagnosis, Differential; Glycin | 2007 |
Chemically induced chorieform activity: antagonism by GABA and EEG patterns.
Topics: Allyl Compounds; Aminobutyrates; Animals; Aspartic Acid; Brain Chemistry; Carbachol; Cats; Caudate N | 1975 |
[Lesch-Nyhan syndrome].
Topics: Aggression; Athetosis; Bites, Human; Chorea; Glycine; Humans; Hyperlipidemias; Intellectual Disabili | 1973 |
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 |