thiamine has been researched along with Decreased Muscle Tone in 4 studies
thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Treatment with thiamine while awaiting the outcome of diagnostic tests may be a good choice." | 1.72 | Case report of two affected siblings in a family with thiamine metabolism dysfunction syndrome 5: a rare, but treatable neurodegenerative disease. ( Chen, H; Chen, Y; Huang, Z; Li, X; Sun, X; Xie, J; Yi, Z; Yu, X; Zhong, J, 2022) |
| "Here, we describe an infant with severe Leigh syndrome, nephrotic syndrome, and CoQ(10) deficiency in muscle and fibroblasts and compound heterozygous mutations in the PDSS2 gene, which encodes a subunit of decaprenyl diphosphate synthase, the first enzyme of the CoQ(10) biosynthetic pathway." | 1.33 | Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations. ( Dimauro, S; Hirano, M; Kanki, T; López, LC; Naini, A; Quinzii, CM; Rodenburg, RJ; Schuelke, M, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Li, X | 1 |
| Huang, Z | 1 |
| Chen, Y | 1 |
| Sun, X | 1 |
| Yi, Z | 1 |
| Xie, J | 1 |
| Yu, X | 1 |
| Chen, H | 1 |
| Zhong, J | 1 |
| Saini, M | 1 |
| Lin, W | 1 |
| Kang, C | 1 |
| Umapathi, T | 1 |
| Netravathi, M | 1 |
| Sinha, S | 1 |
| Taly, AB | 1 |
| Bindu, PS | 1 |
| Bharath, RD | 1 |
| López, LC | 1 |
| Schuelke, M | 1 |
| Quinzii, CM | 1 |
| Kanki, T | 1 |
| Rodenburg, RJ | 1 |
| Naini, A | 1 |
| Dimauro, S | 1 |
| Hirano, M | 1 |
4 other studies available for thiamine and Decreased Muscle Tone
| Article | Year |
|---|---|
Case report of two affected siblings in a family with thiamine metabolism dysfunction syndrome 5: a rare, but treatable neurodegenerative disease.
Topics: Ataxia; Brain Diseases; Humans; Male; Muscle Hypotonia; Mutation; Neurodegenerative Diseases; Siblin | 2022 |
Acute flaccid paralysis: Do not forget beriberi neuropathy.
Topics: Acute Disease; Adult; Beriberi; Female; Guillain-Barre Syndrome; Humans; Male; Middle Aged; Muscle H | 2019 |
Hyperemesis-gravidarum-induced Wernicke's encephalopathy: serial clinical, electrophysiological and MR imaging observations.
Topics: Adult; Female; Humans; Hyperemesis Gravidarum; Medulla Oblongata; Muscle Hypotonia; Neural Conductio | 2009 |
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations.
Topics: Alkyl and Aryl Transferases; Biotin; Carnitine; Case-Control Studies; Cells, Cultured; Coenzymes; Fi | 2006 |