glycine has been researched along with Adult-Onset Dystonias in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kutschenko, A | 1 |
| Staege, S | 1 |
| Grütz, K | 1 |
| Glaß, H | 1 |
| Kalmbach, N | 1 |
| Gschwendtberger, T | 1 |
| Henkel, LM | 1 |
| Heine, J | 1 |
| Grünewald, A | 1 |
| Hermann, A | 1 |
| Seibler, P | 1 |
| Wegner, F | 1 |
| Hirzel, K | 1 |
| Müller, U | 1 |
| Latal, AT | 1 |
| Hülsmann, S | 1 |
| Grudzinska, J | 1 |
| Seeliger, MW | 1 |
| Betz, H | 1 |
| Laube, B | 1 |
| Asmus, F | 1 |
| Devlin, A | 1 |
| Munz, M | 1 |
| Zimprich, A | 1 |
| Gasser, T | 1 |
| Chinnery, PF | 1 |
| Lu, CS | 1 |
| Chang, HC | 1 |
| Weng, YH | 1 |
| Chen, RS | 1 |
| Bonifati, V | 1 |
| Wu-Chou, YH | 1 |
4 other studies available for glycine and Adult-Onset Dystonias
| Article | Year |
|---|---|
Functional and Molecular Properties of DYT-SGCE Myoclonus-Dystonia Patient-Derived Striatal Medium Spiny Neurons.
Topics: Acetylcholine; Action Potentials; Adult; Calcium Channel Blockers; Calcium Channels, L-Type; Calcium | 2021 |
Hyperekplexia phenotype of glycine receptor alpha1 subunit mutant mice identifies Zn(2+) as an essential endogenous modulator of glycinergic neurotransmission.
Topics: Animals; Brain Stem; Cell Line; Chimera; Disease Models, Animal; Dystonic Disorders; Efferent Pathwa | 2006 |
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 |
Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Child; DNA Mutational Analysis; Dystonic Disor | 2008 |