Page last updated: 2024-08-17

coenzyme a and Iron Metabolism Disorders

coenzyme a has been researched along with Iron Metabolism Disorders in 3 studies

Research

Studies (3)

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

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

Reviews

1 review(s) available for coenzyme a and Iron Metabolism Disorders

Article	Year
Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms. Annual review of genomics and human genetics, 2015, Volume: 16 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

Article

Year

Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms.

Annual review of genomics and human genetics, 2015, Volume: 16

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

Other Studies

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. Molecular genetics and metabolism, 2012, Volume: 105, Issue:3 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. Neurology, 2005, May-24, Volume: 64, Issue:10 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

Article

Year

Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations.

Molecular genetics and metabolism, 2012, Volume: 105, Issue:3

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.

Neurology, 2005, May-24, Volume: 64, Issue:10

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