coenzyme a has been researched along with Iron Metabolism Disorders in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hayflick, SJ; Kurian, MA; Meyer, E | 1 |
Bertini, E; Caccia, C; Ciusani, E; Clish, CB; Deik, A; Dusi, S; Garavaglia, B; Leoni, V; Mootha, VK; Nardocci, N; Rimoldi, M; Souza, AL; Strittmatter, L; Tiranti, V; Venco, P; Zibordi, F; Zorzi, G | 1 |
Albanese, A; Barone, P; Bentivoglio, AR; Bonuccelli, U; Cif, L; Coubes, P; D'Amico, A; Dallapiccola, B; Di Giorgio, A; Marelli, C; Pellecchia, MT; Salvi, S; Scarano, V; Valente, EM | 1 |
1 review(s) available for coenzyme a and Iron Metabolism Disorders
Article | Year |
---|---|
Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms.
Topics: Animals; Autophagy; Brain; Ceruloplasmin; Coenzyme A; Genetic Variation; Group VI Phospholipases A2; Humans; Iron; Iron Metabolism Disorders; Lipid Metabolism; Mice; Mitochondrial Proteins; Neuroaxonal Dystrophies; Neurodegenerative Diseases; Parkinsonian Disorders | 2015 |
2 other study(ies) available for coenzyme a and Iron Metabolism Disorders
Article | Year |
---|---|
Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations.
Topics: Adolescent; Adult; Bile Acids and Salts; Child; Child, Preschool; Codon, Nonsense; Coenzyme A; Cohort Studies; Female; Humans; Iron Metabolism Disorders; Lactic Acid; Lipid Metabolism; Lipid Metabolism Disorders; Male; Metabolome; Mitochondria; Neuroaxonal Dystrophies; Pantothenate Kinase-Associated Neurodegeneration; Pantothenic Acid; Phosphotransferases (Alcohol Group Acceptor); Sphingomyelins; Young Adult | 2012 |
The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration.
Topics: Adolescent; Adult; Brain Diseases, Metabolic, Inborn; Child; Coenzyme A; DNA Mutational Analysis; Female; Genetic Testing; Globus Pallidus; Heredodegenerative Disorders, Nervous System; Humans; Iron; Iron Metabolism Disorders; Male; Mental Disorders; Middle Aged; Mutation; Obsessive-Compulsive Disorder; Pantothenate Kinase-Associated Neurodegeneration; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Pyramidal Tracts; Tics | 2005 |