lactic acid has been researched along with Cerebellar Ataxia 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.
Cerebellar Ataxia: Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
Excerpt | Relevance | Reference |
---|---|---|
"Maternally inherited diabetes and deafness (MIDD) and myoencephalopathy, lactic acidosis, stroke-like episodes (MELAS) syndromes are characterized by the same A3243G mutation of mitochondrial DNA (mtDNA)." | 3.75 | Brain anomalies in maternally inherited diabetes and deafness syndrome. ( Cozzone, PJ; Felician, O; Fromont, I; Lebail, B; Lefur, Y; Mancini, J; Nicoli, F; Paquis-Flucklinger, V; Valéro, R; Vialettes, B, 2009) |
"Inherited ataxias are a group of heterogeneous disorders in children or adults but their genetic definition remains still undetermined in almost half of the patients." | 1.43 | Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3. ( Barca, E; DiMauro, S; Granata, F; Marino, S; Montagnese, F; Musumeci, O; Nunnari, D; Peverelli, L; Quinzii, CM; Toscano, A, 2016) |
"Cerebellar ataxia is known to occasionally occur in the course of mitochondrial disorders." | 1.35 | 1H MRS spectroscopy evidence of cerebellar high lactate in mitochondrial respiratory chain deficiency. ( Bahi-Buisson, N; Boddaert, N; Brami-Zylberberg, F; Brunelle, F; de Lonlay, P; Desguerre, I; Funalot, B; Lebre, AS; Munnich, A; Rio, M; Romano, S; Rötig, A; Sarzi, E; Seidenwurm, D; Valayannopoulos, V, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Rumyantseva, A | 1 |
Motori, E | 1 |
Trifunovic, A | 1 |
Márquez, G | 1 |
Romero-Arenas, S | 1 |
Marín-Pagán, C | 1 |
Vera-Ibañez, A | 1 |
FernáNdez Del Olmo, M | 1 |
Taube, W | 1 |
Barca, E | 1 |
Musumeci, O | 1 |
Montagnese, F | 1 |
Marino, S | 1 |
Granata, F | 1 |
Nunnari, D | 1 |
Peverelli, L | 1 |
DiMauro, S | 1 |
Quinzii, CM | 1 |
Toscano, A | 1 |
Fromont, I | 1 |
Nicoli, F | 1 |
Valéro, R | 1 |
Felician, O | 1 |
Lebail, B | 1 |
Lefur, Y | 1 |
Mancini, J | 1 |
Paquis-Flucklinger, V | 1 |
Cozzone, PJ | 1 |
Vialettes, B | 1 |
Jurkiewicz, E | 1 |
Mierzewska, H | 1 |
Bekiesińska-Figatowska, M | 1 |
Pakua-Kościesza, I | 1 |
Kmieć, T | 1 |
Scheper, G | 1 |
van der Knaap, MS | 1 |
Pronicka, E | 1 |
Boddaert, N | 1 |
Romano, S | 1 |
Funalot, B | 1 |
Rio, M | 1 |
Sarzi, E | 1 |
Lebre, AS | 1 |
Bahi-Buisson, N | 1 |
Valayannopoulos, V | 1 |
Desguerre, I | 2 |
Seidenwurm, D | 1 |
Brunelle, F | 1 |
Brami-Zylberberg, F | 1 |
Rötig, A | 1 |
Munnich, A | 1 |
de Lonlay, P | 1 |
Boitier, E | 1 |
Degoul, F | 1 |
Charpentier, C | 1 |
François, D | 1 |
Ponsot, G | 1 |
Diry, M | 1 |
Rustin, P | 1 |
Marsac, C | 1 |
7 other studies available for lactic acid and Cerebellar Ataxia
Article | Year |
---|---|
DARS2 is indispensable for Purkinje cell survival and protects against cerebellar ataxia.
Topics: Animals; Aspartate-tRNA Ligase; Brain Stem; Cell Survival; Cerebellar Ataxia; Cerebellum; Humans; La | 2020 |
Peripheral and central fatigue after high intensity resistance circuit training.
Topics: Case-Control Studies; Cerebellar Ataxia; Circuit-Based Exercise; Female; Humans; Lactic Acid; Male; | 2017 |
Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3.
Topics: Ataxia; Cerebellar Ataxia; Codon, Nonsense; Delayed Diagnosis; Electron Transport Chain Complex Prot | 2016 |
Brain anomalies in maternally inherited diabetes and deafness syndrome.
Topics: Adult; Aged; Brain; Cerebellar Ataxia; Cognition Disorders; Deafness; Diabetes Mellitus; Diabetes Me | 2009 |
MRI of a family with leukoencephalypathy with vanishing white matter.
Topics: Adolescent; Amino Acid Substitution; Aspartic Acid; Brain; Case-Control Studies; Cerebellar Ataxia; | 2005 |
1H MRS spectroscopy evidence of cerebellar high lactate in mitochondrial respiratory chain deficiency.
Topics: Adolescent; Cerebellar Ataxia; Cerebellum; Child; Child, Preschool; Humans; Infant; Infant, Newborn; | 2008 |
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency.
Topics: Cerebellar Ataxia; Child, Preschool; Coenzymes; Electron Transport; Epilepsy; Humans; Kinetics; Lact | 1998 |