Page last updated: 2024-08-17

coenzyme a and Movement Disorders

coenzyme a has been researched along with Movement Disorders in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Cances, C; Damaj, L; de Lonlay, P; Doummar, D; Espil, C; Fluss, J; François-Heude, MC; Kern, I; Lebigot, E; Leboucq, N; Lenaers, G; Meyer, P; Munnich, A; Roubertie, A; Roze, E; Spitz, MA; Torre, S; Touati, G; Warde, MTA	1
Cai, Y; Cronin, CN; Engel, AG; Hersh, LB; Ohno, K; Rodgers, DW	1
Marsac, C; Stansbie, D; Wallace, SJ	1

Reviews

1 review(s) available for coenzyme a and Movement Disorders

Article	Year
Disorders of the pyruvate dehydrogenase complex. Journal of inherited metabolic disease, 1986, Volume: 9, Issue:2 Topics: Acetyl Coenzyme A; Acetyltransferases; Acidosis; Brain; Carbon Dioxide; Child; Child, Preschool; Coenzyme A; Cranial Nerves; Dihydrolipoamide Dehydrogenase; Dihydrolipoyllysine-Residue Acetyltransferase; Facial Bones; Feedback; Humans; Lactates; Lactic Acid; Leigh Disease; Molecular Weight; Movement Disorders; NAD; Nervous System Diseases; Phosphoric Monoester Hydrolases; Pyruvate Decarboxylase; Pyruvate Dehydrogenase Complex; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Pyruvic Acid; Spectrophotometry	1986

Article

Year

Disorders of the pyruvate dehydrogenase complex.

Journal of inherited metabolic disease, 1986, Volume: 9, Issue:2

Topics: Acetyl Coenzyme A; Acetyltransferases; Acidosis; Brain; Carbon Dioxide; Child; Child, Preschool; Coenzyme A; Cranial Nerves; Dihydrolipoamide Dehydrogenase; Dihydrolipoyllysine-Residue Acetyltransferase; Facial Bones; Feedback; Humans; Lactates; Lactic Acid; Leigh Disease; Molecular Weight; Movement Disorders; NAD; Nervous System Diseases; Phosphoric Monoester Hydrolases; Pyruvate Decarboxylase; Pyruvate Dehydrogenase Complex; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Pyruvic Acid; Spectrophotometry

1986

Other Studies

2 other study(ies) available for coenzyme a and Movement Disorders

Article	Year
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies. European journal of neurology, 2022, Volume: 29, Issue:11 Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Chorea; Coenzyme A; Dystonia; Dystonic Disorders; Enoyl-CoA Hydratase; Humans; Leigh Disease; Movement Disorders; Thiolester Hydrolases; Valine	2022
Choline acetyltransferase structure reveals distribution of mutations that cause motor disorders. The EMBO journal, 2004, May-19, Volume: 23, Issue:10 Topics: Amino Acid Sequence; Animals; Binding Sites; Choline O-Acetyltransferase; Coenzyme A; Crystallography, X-Ray; Humans; Models, Molecular; Molecular Sequence Data; Molecular Structure; Movement Disorders; Mutation; Protein Conformation; Rats; Sequence Alignment	2004

Article

Year

Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies.

European journal of neurology, 2022, Volume: 29, Issue:11

Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Chorea; Coenzyme A; Dystonia; Dystonic Disorders; Enoyl-CoA Hydratase; Humans; Leigh Disease; Movement Disorders; Thiolester Hydrolases; Valine

2022

Choline acetyltransferase structure reveals distribution of mutations that cause motor disorders.

The EMBO journal, 2004, May-19, Volume: 23, Issue:10

Topics: Amino Acid Sequence; Animals; Binding Sites; Choline O-Acetyltransferase; Coenzyme A; Crystallography, X-Ray; Humans; Models, Molecular; Molecular Sequence Data; Molecular Structure; Movement Disorders; Mutation; Protein Conformation; Rats; Sequence Alignment

2004