leucine has been researched along with Cardiomyopathies in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (37.50) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 1 (12.50) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Allard, P; Furtos, A; Mitchell, GA; Nuyt, AM; Paradis, P; Ryan, RO; Schiffrin, EL; Tang, MC; Wang, S; Wang, Y; Waters, P; Yang, H | 1 |
| León-Ruiz, EN; Robbins, KA | 1 |
| Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E | 1 |
| Aime, B; Bouvagnet, P; Bozio, A; Bruyère, P; Chalabreysse, L; Ollagnier, C; Senni, F | 1 |
| el-Gewely, MR; Husby, G; Nordvåg, BY; Ranløv, I; Riise, HM | 1 |
| Barakat, HA; Brown, WE; Dohm, GL | 1 |
| Evans, C; Oratz, M; Reff, F; Rothschild, MA; Schreiber, SS | 1 |
| Brink, A; Brink, AJ; Lochner, A | 1 |
8 other study(ies) available for leucine and Cardiomyopathies
| Article | Year |
|---|---|
Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers.
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Biomarkers; Cardiomyopathies; Leucine; Mice | 2022 |
Anesthetic management of a patient with 3-methylcrotonyl-CoA carboxylase deficiency.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Anesthesia, General; Carbon-Carbon Ligases; Cardiomyopathies; Carnitine; Female; Humans; Leucine | 2008 |
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult | 2009 |
A new hypo/oligodontia syndrome: Carvajal/Naxos syndrome secondary to desmoplakin-dominant mutations.
Topics: Adolescent; Amino Acid Sequence; Anodontia; Arrhythmogenic Right Ventricular Dysplasia; Bicuspid; Cardiomyopathies; Cardiomyopathy, Dilated; Conserved Sequence; Cytosine; Desmoplakins; Follow-Up Studies; gamma Catenin; Genes, Dominant; Hair Diseases; Humans; Incisor; Keratoderma, Palmoplantar; Leucine; Male; Molar; Molar, Third; Mutation, Missense; Pedigree; Serine; Thymine | 2011 |
Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissues.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amyloidosis; Cardiomyopathies; Child, Preschool; Denmark; DNA-Cytosine Methylases; Female; Formaldehyde; Humans; Leucine; Male; Methionine; Middle Aged; Oligodeoxyribonucleotides; Paraffin Embedding; Point Mutation; Polymerase Chain Reaction; Prealbumin; Retrospective Studies; Tissue Fixation; Tissue Survival | 1993 |
Oxidation of leucine by heart and muscle homogenates of the cardiomyopathic hamster.
Topics: Age Factors; Animals; Cardiomyopathies; Cricetinae; Leucine; Muscles; Myocardium; Oxidation-Reduction; Transaminases | 1977 |
Alcoholic cardiomyopathy. II. The inhibition of cardiac microsomal protein synthesis by acetaldehyde.
Topics: Acetaldehyde; Animals; Carbon Radioisotopes; Cardiomyopathies; Cell-Free System; Depression, Chemical; Ethanol; Guinea Pigs; In Vitro Techniques; Leucine; Lysine; Microsomes; Muscle Proteins; Myocardium; Perfusion; RNA; Time Factors | 1974 |
Protein synthesis in the myocardiopathy and muscular dystrophy of the Syrian hamster.
Topics: Animals; Carbon Isotopes; Cardiomyopathies; Cricetinae; Diaphragm; Female; In Vitro Techniques; Leucine; Lysine; Male; Muscle Proteins; Muscles; Muscular Dystrophy, Animal; Myocardium; Tritium | 1971 |