glycine has been researched along with Chorea Disorders in 9 studies
| 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 Disorders
| Article | Year |
|---|---|
Neurotransmitter synthetic enzymes.
Topics: Acetylcholine; Acetyltransferases; Adenylyl Cyclases; Aging; Aminobutyrates; Animals; Brain; Brain C | 1973 |
1 trial available for glycine and Chorea Disorders
| 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 Disorders
| 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 |