Page last updated: 2024-10-17

lactic acid and Adiadochokinesis

lactic acid has been researched along with Adiadochokinesis 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.

Research Excerpts

ExcerptRelevanceReference
"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)."3.75Brain 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."1.43Cerebellar 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."1.351H 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)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's3 (42.86)29.6817
2010's2 (28.57)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
Rumyantseva, A1
Motori, E1
Trifunovic, A1
Márquez, G1
Romero-Arenas, S1
Marín-Pagán, C1
Vera-Ibañez, A1
FernáNdez Del Olmo, M1
Taube, W1
Barca, E1
Musumeci, O1
Montagnese, F1
Marino, S1
Granata, F1
Nunnari, D1
Peverelli, L1
DiMauro, S1
Quinzii, CM1
Toscano, A1
Fromont, I1
Nicoli, F1
Valéro, R1
Felician, O1
Lebail, B1
Lefur, Y1
Mancini, J1
Paquis-Flucklinger, V1
Cozzone, PJ1
Vialettes, B1
Jurkiewicz, E1
Mierzewska, H1
Bekiesińska-Figatowska, M1
Pakua-Kościesza, I1
Kmieć, T1
Scheper, G1
van der Knaap, MS1
Pronicka, E1
Boddaert, N1
Romano, S1
Funalot, B1
Rio, M1
Sarzi, E1
Lebre, AS1
Bahi-Buisson, N1
Valayannopoulos, V1
Desguerre, I2
Seidenwurm, D1
Brunelle, F1
Brami-Zylberberg, F1
Rötig, A1
Munnich, A1
de Lonlay, P1
Boitier, E1
Degoul, F1
Charpentier, C1
François, D1
Ponsot, G1
Diry, M1
Rustin, P1
Marsac, C1

Other Studies

7 other studies available for lactic acid and Adiadochokinesis

ArticleYear
DARS2 is indispensable for Purkinje cell survival and protects against cerebellar ataxia.
    Human molecular genetics, 2020, 10-10, Volume: 29, Issue:17

    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.
    Muscle & nerve, 2017, Volume: 56, Issue:1

    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.
    Clinical genetics, 2016, Volume: 90, Issue:2

    Topics: Ataxia; Cerebellar Ataxia; Codon, Nonsense; Delayed Diagnosis; Electron Transport Chain Complex Prot

2016
Brain anomalies in maternally inherited diabetes and deafness syndrome.
    Journal of neurology, 2009, Volume: 256, Issue:10

    Topics: Adult; Aged; Brain; Cerebellar Ataxia; Cognition Disorders; Deafness; Diabetes Mellitus; Diabetes Me

2009
MRI of a family with leukoencephalypathy with vanishing white matter.
    Pediatric radiology, 2005, Volume: 35, Issue:10

    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.
    Molecular genetics and metabolism, 2008, Volume: 93, Issue:1

    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.
    Journal of the neurological sciences, 1998, Volume: 156, Issue:1

    Topics: Cerebellar Ataxia; Child, Preschool; Coenzymes; Electron Transport; Epilepsy; Humans; Kinetics; Lact

1998