Page last updated: 2024-08-18

pyrroles and Purine Pyrimidine Metabolism, Inborn Errors

pyrroles has been researched along with Purine Pyrimidine Metabolism, Inborn Errors in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
García-Estévez, DA; Navarro, C; San Millán, B; Sogo, T	1

Other Studies

1 other study(ies) available for pyrroles and Purine Pyrimidine Metabolism, Inborn Errors

Article	Year
[Myopathy due to deficiency of desaminase myoadenilate induced by atorvastatine]. Medicina clinica, 2013, Jun-18, Volume: 140, Issue:12 Topics: Aged; Amino Acid Substitution; AMP Deaminase; Atorvastatin; Biopsy; Causality; Creatine Kinase, MM Form; Exercise Tolerance; Female; Heptanoic Acids; Homozygote; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypercholesterolemia; Liver-Specific Organic Anion Transporter 1; Mitochondria, Muscle; Models, Genetic; Muscle, Skeletal; Mutation, Missense; Myalgia; Organic Anion Transporters; Parkinsonian Disorders; Point Mutation; Polymorphism, Single Nucleotide; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrroles; Ubiquinone	2013

Article

Year

[Myopathy due to deficiency of desaminase myoadenilate induced by atorvastatine].

Medicina clinica, 2013, Jun-18, Volume: 140, Issue:12

Topics: Aged; Amino Acid Substitution; AMP Deaminase; Atorvastatin; Biopsy; Causality; Creatine Kinase, MM Form; Exercise Tolerance; Female; Heptanoic Acids; Homozygote; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypercholesterolemia; Liver-Specific Organic Anion Transporter 1; Mitochondria, Muscle; Models, Genetic; Muscle, Skeletal; Mutation, Missense; Myalgia; Organic Anion Transporters; Parkinsonian Disorders; Point Mutation; Polymorphism, Single Nucleotide; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrroles; Ubiquinone

2013