lactic acid has been researched along with Epilepsies, Myoclonic in 7 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.
Epilepsies, Myoclonic: A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A case of a unique combination of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like syndrome (MELAS) with acanthocytosis is reported." | 7.67 | Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case. ( Kazui, H; Mukoyama, M; Nonaka, I; Satoyoshi, E; Sunohara, N; Yoshida, M, 1986) |
| "A case of a unique combination of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like syndrome (MELAS) with acanthocytosis is reported." | 3.67 | Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case. ( Kazui, H; Mukoyama, M; Nonaka, I; Satoyoshi, E; Sunohara, N; Yoshida, M, 1986) |
| "The disorders causing myoclonus have been compared to those in which myoclonus has been reported." | 2.37 | Myoclonus and mitochondrial myopathy. ( Hopkins, LC; Rosing, HS, 1986) |
| "At 3 years old, astatic myoclonic epilepsy appeared, with no response to levetiracetam." | 1.43 | Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient. ( García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O, 2016) |
| "Characteristics of myoclonic epilepsy associated with ragged-red fibers include myoclonic epilepsy, generalized epilepsy, hearing loss, exercise intolerance, lactic acidosis, and ragged-red fibers." | 1.35 | Myoclonic epilepsy with ragged-red fibers without increased lactate levels. ( Kimura, S; Kosuge, H; Nakamura, K; Nomura, K; Ozasa, S, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tort, F | 1 |
| Ugarteburu, O | 1 |
| Torres, MA | 1 |
| García-Villoria, J | 1 |
| Girós, M | 1 |
| Ruiz, A | 1 |
| Ribes, A | 1 |
| Kimura, S | 1 |
| Ozasa, S | 1 |
| Nakamura, K | 1 |
| Nomura, K | 1 |
| Kosuge, H | 1 |
| Arpa, J | 1 |
| Cruz-Martínez, A | 1 |
| Campos, Y | 1 |
| Gutiérrez-Molina, M | 1 |
| García-Rio, F | 1 |
| Pérez-Conde, C | 1 |
| Martín, MA | 1 |
| Rubio, JC | 1 |
| Del Hoyo, P | 1 |
| Arpa-Fernández, A | 1 |
| Arenas, J | 1 |
| van Hellenberg Hubar, JL | 1 |
| Gabreëls, FJ | 1 |
| Ruitenbeek, W | 1 |
| Sengers, RC | 1 |
| Renier, WO | 1 |
| Thijssen, HO | 1 |
| ter Laak, HJ | 1 |
| Mukoyama, M | 1 |
| Kazui, H | 1 |
| Sunohara, N | 1 |
| Yoshida, M | 1 |
| Nonaka, I | 1 |
| Satoyoshi, E | 1 |
| Mizuno, Y | 1 |
| Ishiguro, K | 1 |
| Okamoto, K | 1 |
| Morimatsu, M | 1 |
| Hirai, S | 1 |
| Hopkins, LC | 1 |
| Rosing, HS | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Nutritional Assessment in Patients Affected by Mitochondrial Cytopathy[NCT02375438] | 26 participants (Actual) | Observational | 2014-12-31 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 reviews available for lactic acid and Epilepsies, Myoclonic
| Article | Year |
|---|---|
MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
Topics: Biopsy; Child; Child, Preschool; Electroencephalography; Electromyography; Energy Metabolism; Enzyme | 1991 |
Myoclonus and mitochondrial myopathy.
Topics: Adolescent; Brain Diseases, Metabolic; Central Nervous System Diseases; Electroencephalography; Epil | 1986 |
5 other studies available for lactic acid and Epilepsies, Myoclonic
| Article | Year |
|---|---|
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine | 2016 |
Myoclonic epilepsy with ragged-red fibers without increased lactate levels.
Topics: Adolescent; Anticonvulsants; Diagnosis, Differential; DNA Mutational Analysis; DNA, Mitochondrial; E | 2009 |
Prevalence and progression of mitochondrial diseases: a study of 50 patients.
Topics: Adolescent; Adult; Age of Onset; Aged; Disease Progression; DNA, Mitochondrial; Electromyography; Ep | 2003 |
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case.
Topics: Acanthocytes; Acidosis; Adult; Aphasia; Atrophy; Biopsy; Cerebellum; Cerebral Cortex; Cerebral Ventr | 1986 |
[A case of mitochondrial encephalomyopathy characterized by repeated stroke-like episodes].
Topics: Adult; Brain Diseases; Cerebrovascular Disorders; Electroencephalography; Epilepsies, Myoclonic; Hum | 1989 |