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lactic acid and Basal Ganglia Diseases

lactic acid has been researched along with Basal Ganglia Diseases in 6 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.

Basal Ganglia Diseases: Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.

Research Excerpts

ExcerptRelevanceReference
"Both patients had PDH deficiency caused by a new mutation (G585C) in the PDHA1 gene, which is predicted to replace a highly conserved glycine at codon 195 by alanine."1.35Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia. ( Debray, FG; Gagne, R; Laframboise, R; Lambert, M; MacKay, N; Maranda, B; Mitchell, GA; Robinson, BH, 2008)
"We report a new case of MERRF (myoclonus epilepsy with ragged red fibers) syndrome with basal nuclei calcification on the brain CT scan, without hormonal abnormalities, with high CSF protein and hyperlactacidemia, juvenile onset and death at 18 years."1.27Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia. ( Cornelio, F; Di Donato, S; Ederli, E; Fabrizi, GM; Federico, A; Guazzi, GC; Manneschi, L, 1988)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lagrue, E1
Abert, B1
Nadal, L1
Tabone, L1
Bodard, S1
Medja, F1
Lombes, A1
Chalon, S1
Castelnau, P1
Vokaer, M1
Bier, JC1
David, P1
Grand, S1
Supiot, F1
Ventura, M1
Bartholomé, EJ1
Morava, E1
Rodenburg, RJ1
Hol, F1
de Vries, M1
Janssen, A1
van den Heuvel, L1
Nijtmans, L1
Smeitink, J1
Debray, FG1
Lambert, M1
Gagne, R1
Maranda, B1
Laframboise, R1
MacKay, N1
Robinson, BH1
Mitchell, GA1
Federico, A1
Cornelio, F1
Di Donato, S1
Ederli, E1
Fabrizi, GM1
Manneschi, L1
Guazzi, GC1
Al-Mateen, M1
Philippart, M1
Shields, WD1

Other Studies

6 other studies available for lactic acid and Basal Ganglia Diseases

ArticleYear
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood.
    Metabolic brain disease, 2009, Volume: 24, Issue:2

    Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Basal Ganglia; Basal Ganglia Diseases; Diseas

2009
Striatal lesions: an underestimated complication of cerebral malaria?
    European journal of neurology, 2004, Volume: 11, Issue:10

    Topics: Adult; Animals; Basal Ganglia Diseases; Corpus Striatum; Humans; Lactic Acid; Magnetic Resonance Ima

2004
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations.
    American journal of medical genetics. Part A, 2006, Apr-15, Volume: 140, Issue:8

    Topics: Adenosine Triphosphate; Alanine; Basal Ganglia Diseases; Child; Child, Preschool; DNA, Mitochondrial

2006
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia.
    Neuropediatrics, 2008, Volume: 39, Issue:1

    Topics: Ataxia; Basal Ganglia Diseases; Binding Sites; Brain Diseases, Metabolic; Child; Child, Preschool; D

2008
Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia.
    Italian journal of neurological sciences, 1988, Volume: 9, Issue:1

    Topics: Adolescent; Basal Ganglia Diseases; Calcinosis; Epilepsy; Humans; Lactates; Lactic Acid; Male; Mitoc

1988
Rett syndrome. A commonly overlooked progressive encephalopathy in girls.
    American journal of diseases of children (1960), 1986, Volume: 140, Issue:8

    Topics: Adolescent; Adult; Ataxia; Basal Ganglia Diseases; Brain Diseases; Child; Child, Preschool; Dementia

1986