lactic acid has been researched along with Myotonic Dystrophy in 8 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
Myotonic Dystrophy: Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (12.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 5 (62.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baldanzi, S | 1 |
| Ricci, G | 1 |
| Bottari, M | 1 |
| Chico, L | 1 |
| Simoncini, C | 1 |
| Siciliano, G | 2 |
| Gao, Z | 1 |
| Cooper, TA | 1 |
| Lovadi, E | 1 |
| Csereklyei, M | 1 |
| Merkli, H | 1 |
| FüLöp, K | 1 |
| Sebők, Á | 1 |
| Karcagi, V | 1 |
| Komoly, S | 1 |
| Pál, E | 1 |
| Owen, PM | 1 |
| Chu, C | 1 |
| Jakkani, R | 1 |
| Jyoti, S | 1 |
| Ahmed, M | 1 |
| Thomas, MM | 1 |
| Jeppesen, TD | 1 |
| Olsen, D | 1 |
| Vissing, J | 1 |
| KUHN, E | 1 |
| WOERNER, W | 1 |
| Tedeschi, D | 1 |
| Lombardi, V | 1 |
| Mancuso, M | 1 |
| Martelli, F | 1 |
| Sighieri, C | 1 |
| Rocchi, A | 1 |
| Tovani, S | 1 |
| Murri, L | 1 |
8 other studies available for lactic acid and Myotonic Dystrophy
| Article | Year |
|---|---|
The proposal of a clinical protocol to assess central and peripheral fatigue in myotonic dystrophy type 1.
Topics: Adult; Advanced Oxidation Protein Products; Aged; Attention; Case-Control Studies; Clinical Protocol | 2017 |
Reexpression of pyruvate kinase M2 in type 1 myofibers correlates with altered glucose metabolism in myotonic dystrophy.
Topics: Alternative Splicing; Animals; Blotting, Western; Calorimetry, Indirect; Cell Line; Energy Metabolis | 2013 |
Elevated FGF 21 in myotonic dystrophy type 1 and mitochondrial diseases.
Topics: Adult; Aged; Creatine Kinase; Disease Progression; DNA, Mitochondrial; Enzyme-Linked Immunosorbent A | 2017 |
Emergency caesarean section in a patient with myotonic dystrophy: a case of failed postoperative extubation in a patient with mild disease.
Topics: Cardiotocography; Cesarean Section; Female; Humans; Intubation, Intratracheal; Lactic Acid; Myotonic | 2011 |
Magnetic resonance imaging findings in adult-form myotonic dystrophy type 1.
Topics: Adult; Atrophy; Brain; Cataract; Central Nervous System; Electromyography; Hearing Disorders; Humans | 2012 |
Cycle ergometry is not a sensitive diagnostic test for mitochondrial myopathy.
Topics: Adult; Exercise Test; Exercise Tolerance; Female; Humans; Lactic Acid; Male; Mitochondrial Myopathie | 2003 |
[Studies of intermediate metabolism in myotonic dystrophy (lactic acid, pyruvic acid, lactic dehydrogenase and malic acid dehydrogenase)].
Topics: Humans; Lactates; Lactic Acid; Malate Dehydrogenase; Malates; Myotonic Dystrophy; Oxidoreductases; P | 1961 |
Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeutics.
Topics: Coenzymes; Diagnosis, Differential; Energy Metabolism; Humans; Lactic Acid; Mitochondria, Muscle; Mu | 2000 |