isobutyryl-coenzyme-a and Neurodegenerative-Diseases

isobutyryl-coenzyme-a has been researched along with Neurodegenerative-Diseases* in 1 studies

Other Studies

1 other study(ies) available for isobutyryl-coenzyme-a and Neurodegenerative-Diseases

Article	Year
Paroxysmal Dyskinesias Revealing 3-Hydroxy-Isobutyryl-CoA Hydrolase (HIBCH) Deficiency. Neuropediatrics, 2021, Volume: 52, Issue:5 Paroxysmal dyskinesias (PD) are rare movement disorders characterized by recurrent attacks of dystonia, chorea, athetosis, or their combination, with large phenotypic and genetic heterogeneity. 3-Hydroxy-isobutyryl-CoA hydrolase ( Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Chorea; Humans; Neurodegenerative Diseases; Thiolester Hydrolases	2021

Article

Year

Paroxysmal Dyskinesias Revealing 3-Hydroxy-Isobutyryl-CoA Hydrolase (HIBCH) Deficiency.

Neuropediatrics, 2021, Volume: 52, Issue:5

Paroxysmal dyskinesias (PD) are rare movement disorders characterized by recurrent attacks of dystonia, chorea, athetosis, or their combination, with large phenotypic and genetic heterogeneity. 3-Hydroxy-isobutyryl-CoA hydrolase (

Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Chorea; Humans; Neurodegenerative Diseases; Thiolester Hydrolases

2021