beta-alanine has been researched along with Movement Disorders in 3 studies
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 addition, genetic analysis for Dravet syndrome showed the presence of heterozygous disease-causing mutation SCN1A NM_001165963." | 1.42 | NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome. ( Chan, B; Chan, KY; Lai, CK; Lam, CW; Law, CY; Leung, KF; Mak, CM; Pak-lam Chen, S; Yan-wo Chan, A; Yuen, YP, 2015) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Dobritzsch, D | 1 |
| Meijer, J | 1 |
| Meinsma, R | 1 |
| Maurer, D | 1 |
| Monavari, AA | 1 |
| Gummesson, A | 1 |
| Reims, A | 1 |
| Cayuela, JA | 1 |
| Kuklina, N | 1 |
| Benoist, JF | 1 |
| Perrin, L | 1 |
| Assmann, B | 1 |
| Hoffmann, GF | 1 |
| Bierau, J | 1 |
| Kaindl, AM | 1 |
| van Kuilenburg, ABP | 1 |
| Fang, Y | 1 |
| Cai, C | 1 |
| Wang, C | 1 |
| Sun, B | 1 |
| Zhang, X | 1 |
| Fan, W | 1 |
| Hu, W | 1 |
| Meng, Y | 1 |
| Lin, S | 1 |
| Zhang, C | 1 |
| Zhang, Y | 1 |
| Shu, J | 1 |
| Lam, CW | 1 |
| Law, CY | 1 |
| Leung, KF | 1 |
| Lai, CK | 1 |
| Pak-lam Chen, S | 1 |
| Chan, B | 1 |
| Chan, KY | 1 |
| Yuen, YP | 1 |
| Mak, CM | 1 |
| Yan-wo Chan, A | 1 |
3 other studies available for beta-alanine and Movement Disorders
| Article | Year |
|---|---|
β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity.
Topics: Abnormalities, Multiple; Amidohydrolases; Animals; beta-Alanine; Brain Diseases; Humans; Mammals; Mo | 2022 |
Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.
Topics: Abnormalities, Multiple; Amidohydrolases; Aminoisobutyric Acids; Asian People; beta-Alanine; Brain D | 2019 |
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome.
Topics: Abnormalities, Multiple; Amidohydrolases; beta-Alanine; Brain Diseases; Epilepsies, Myoclonic; Gas C | 2015 |