Page last updated: 2024-10-17

lactic acid and Fukuhara Disease

lactic acid has been researched along with Fukuhara Disease in 3 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.

Research Excerpts

ExcerptRelevanceReference
"To evaluate the role of chronic cerebral lactic acidosis in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)."9.11Cerebral lactic acidosis correlates with neurological impairment in MELAS. ( De Vivo, DC; DiMauro, S; Engelstad, K; Hirano, M; Jhung, S; Kaufmann, P; Mao, X; Mitsis, E; Sano, MC; Shanske, S; Shungu, DC, 2004)
"To evaluate the role of chronic cerebral lactic acidosis in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)."5.11Cerebral lactic acidosis correlates with neurological impairment in MELAS. ( De Vivo, DC; DiMauro, S; Engelstad, K; Hirano, M; Jhung, S; Kaufmann, P; Mao, X; Mitsis, E; Sano, MC; Shanske, S; Shungu, DC, 2004)
"Localized brain proton MR spectra were acquired from patients with different mitochondrial encephalomyopathies (myoclonus epilepsy with ragged-red fibers [MERRF], Kearns-Sayre syndrome [KSS], and mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes [MELAS])."3.68Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies. ( Andermann, F; Arnold, DL; Karpati, G; Mathews, PM; Silver, K, 1993)
"Although there seems to be a gene dosage effect in MERRF, we found no absolute relationship between the relative proportion of mutant genomes in blood and clinical severity."1.30Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF). ( Arenas, J; Arpa, J; Barreiro, P; Campos, Y; Cruz-Martínez, A; Gutiérrez-Molina, M; Lacasa, T; López-Pajares, R; Martin-Casanueva, MA; Morales, MC; Pérez-Conde, MC; Tatay, J, 1997)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kaufmann, P1
Shungu, DC1
Sano, MC1
Jhung, S1
Engelstad, K1
Mitsis, E1
Mao, X1
Shanske, S1
Hirano, M1
DiMauro, S1
De Vivo, DC1
Mathews, PM1
Andermann, F1
Silver, K1
Karpati, G1
Arnold, DL1
Arpa, J1
Campos, Y1
Gutiérrez-Molina, M1
Martin-Casanueva, MA1
Cruz-Martínez, A1
Pérez-Conde, MC1
López-Pajares, R1
Morales, MC1
Tatay, J1
Lacasa, T1
Barreiro, P1
Arenas, J1

Trials

1 trial available for lactic acid and Fukuhara Disease

ArticleYear
Cerebral lactic acidosis correlates with neurological impairment in MELAS.
    Neurology, 2004, Apr-27, Volume: 62, Issue:8

    Topics: Acidosis, Lactic; Adult; Blood Glucose; Cerebral Ventricles; Chronic Disease; DNA Mutational Analysi

2004

Other Studies

2 other studies available for lactic acid and Fukuhara Disease

ArticleYear
Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies.
    Neurology, 1993, Volume: 43, Issue:12

    Topics: Aspartic Acid; Brain; Choline; Creatine; Humans; Kearns-Sayre Syndrome; Lactates; Lactic Acid; Magne

1993
Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF).
    Acta neurologica Scandinavica, 1997, Volume: 96, Issue:2

    Topics: Adult; Age of Onset; Creatine Kinase; Disease Progression; DNA, Mitochondrial; Female; Gene Dosage;

1997