methionine has been researched along with Cardiomyopathies, Primary in 20 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (25.00) | 18.7374 |
| 1990's | 9 (45.00) | 18.2507 |
| 2000's | 4 (20.00) | 29.6817 |
| 2010's | 1 (5.00) | 24.3611 |
| 2020's | 1 (5.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bucciantini, M; Caselli, A; Garagna, S; Giorgetti, S; Leri, M; Luti, S; Marchese, L; Natalello, A; Paoli, P; Rebuzzini, P; Stefani, M | 1 |
| Benazzoug, Y; Chaouad, B; Cherifi, MEH; Exbrayat, JM; Ghoul, A; Moudilou, EN; Moulahoum, A; Othmani-Mecif, K; Zerrouk, F | 1 |
| Backman, C; Ihse, E; Lindqvist, P; Suhr, O; Westermark, P; Ybo, A | 1 |
| Baba, HA; Boese, D; Christoph, DC; Erbel, R; Hunold, P; Johnson, KT; Philipp, S; Schlosser, TW | 1 |
| MEERSON, FZ | 1 |
| Kaminari, A; Leze, H; Mamuris, Z; Maridaki, H; Petsiava, E; Stathopoulos, C; Theotokis, P; Zifa, E | 1 |
| Corner, AH; Farnworth, ER; Kramer, JK; Thompson, BK | 1 |
| Clandinin, MT; Yamashiro, S | 1 |
| Husby, G; Nordvåg, BY; Riise, HM | 1 |
| el-Gewely, MR; Husby, G; Nordvåg, BY; Ranløv, I; Riise, HM | 1 |
| Nordvåg, BY; Steensgaard-Hansen, F; Svendsen, IH | 2 |
| Baba, T; Date, Y; Goto, Y; Nakamura, Y; Nakazato, M; Yutani, C | 1 |
| Qu, N; Tian, Y; Xu, J; Zhou, Y | 1 |
| el-Gewely, MR; Husby, G; Nordvåg, BY; Ranløv, I | 1 |
| Benson, MD | 1 |
| Alves, IL; Costa, PP; Husby, G; Ranløv, I; Ranløv, PJ; Saraiva, MJ | 1 |
| Husby, G; Kolset, SO; Magnus, JH; Stenstad, T | 1 |
| Dhalla, NS; Jasmin, G; Okumura, K; Panagia, V | 1 |
| Anan'eva, KA; Golber, LM; Kandror, VI; Kriukova, IV; Negovskaia, AV | 1 |
1 review(s) available for methionine and Cardiomyopathies, Primary
| Article | Year |
|---|---|
[Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. A clinical, genetic and echocardiographic study of an affected Danish family].
Topics: Adolescent; Amyloidosis; Cardiomyopathies; Child; Denmark; Echocardiography, Doppler; Female; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Prealbumin | 1999 |
19 other study(ies) available for methionine and Cardiomyopathies, Primary
| Article | Year |
|---|---|
S-Homocysteinylation effects on transthyretin: worsening of cardiomyopathy onset.
Topics: Amyloid Neuropathies, Familial; Cardiomyopathies; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Homocysteine; Humans; Methionine; Mutation; Myocytes, Cardiac; Prealbumin; Protein Conformation; Protein Stability; Stroke; Structure-Activity Relationship | 2020 |
Hyperhomocysteinemia and myocardial remodeling in the sand rat, Psammomys obesus.
Topics: Animals; Apoptosis; Cardiomyopathies; Gerbillinae; Hyperhomocysteinemia; Methionine; Muscle Proteins; Myocardium; Myocytes, Cardiac | 2019 |
Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis.
Topics: Abdominal Fat; Adult; Age of Onset; Amino Acid Substitution; Amyloid; Amyloidosis, Familial; Blotting, Western; Cardiomyopathies; Echocardiography; Electrophoresis, Polyacrylamide Gel; Female; Heart Septal Defects, Ventricular; Humans; Male; Methionine; Middle Aged; Prealbumin; Sweden; Valine | 2008 |
Heart failure and cardiac involvement as isolated manifestation of familial form of transthyretin amyloidosis resulting from Val30Met mutation with no clinical signs of polyneuropathy.
Topics: Amyloidosis, Familial; Cardiomyopathies; Echocardiography; Heart Failure; Humans; Immunohistochemistry; Magnetic Resonance Imaging; Male; Methionine; Microscopy, Electron; Middle Aged; Mutation; Prealbumin; Valine | 2009 |
A MECHANISM OF HYPERTROPHY AND WEAR OF THE MYOCARDIUM.
Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Aortic Valve Stenosis; Cardiomegaly; Cardiomyopathies; DNA; Dogs; Folic Acid; Humans; Hypertrophy; Methionine; Muscle Proteins; Myocardium; Nucleic Acids; Nucleosides; Orotic Acid; Pharmacology; Rabbits; Rats; Research; Strophanthins; Vitamin B 12 | 1965 |
A novel G3337A mitochondrial ND1 mutation related to cardiomyopathy co-segregates with tRNALeu(CUN) A12308G and tRNAThr C15946T mutations.
Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Cardiomyopathies; Case-Control Studies; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Family; Female; Genetic Predisposition to Disease; Humans; Infant, Newborn; Methionine; Mitochondria; Molecular Sequence Data; Molecular Structure; Mutation; NADH Dehydrogenase; Pedigree; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary; RNA, Transfer, Leu; RNA, Transfer, Thr | 2008 |
The methionine and choline status of rat diets and their effects on nutrition and myocardial lesions.
Topics: Animal Nutritional Physiological Phenomena; Animals; Cardiomyopathies; Caseins; Choline; Dietary Proteins; Glycine max; Lipid Metabolism; Liver; Male; Methionine; Myocardium; Organ Size; Rats; Rats, Inbred Strains; Weaning | 1983 |
Effects of methionine supplementation on the incidence of dietary fat induced myocardial lesions in the rat.
Topics: Amino Acids, Sulfur; Animals; Brassica; Cardiomyopathies; Cystine; Diet; Dietary Fats; Energy Intake; Erucic Acids; Glycine max; Methionine; Nutritional Requirements; Rats | 1980 |
Verification of the transthyretin Met 111 mutation in familial amyloid cardiomyopathy of Danish origin by DNA sequencing.
Topics: Amyloid; Base Sequence; Cardiomyopathies; DNA Primers; Humans; Methionine; Molecular Sequence Data; Mutation; Prealbumin; Sequence Analysis, DNA | 1994 |
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 |
A clinical, echocardiographic and genetic characterization of a Danish kindred with familial amyloid transthyretin methionine 111 linked cardiomyopathy.
Topics: Adolescent; Adult; Aged; Amyloidosis; Cardiomyopathies; Cardiomyopathy, Restrictive; Carpal Tunnel Syndrome; Child; DNA Mutational Analysis; Female; Genetic Carrier Screening; Genetic Linkage; Genotype; Humans; Male; Methionine; Middle Aged; Pedigree; Prealbumin; Ultrasonography; Ventricular Function, Left | 1998 |
A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
Topics: Aged; Amyloid Neuropathies; Amyloidosis; Base Sequence; Cardiomyopathies; Female; Giant Cells; Heart Ventricles; Humans; Methionine; Point Mutation; Prealbumin; Rectum | 1999 |
[Effect of methionine supplementation on the selenium bioavailability in rats fed on grains from Keshan disease endemic area].
Topics: Animals; Biological Availability; Cardiomyopathies; Edible Grain; Glutathione Peroxidase; Male; Methionine; Random Allocation; Rats; Rats, Wistar; Selenium | 2001 |
Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.
Topics: Amyloidosis; Base Sequence; Cardiomyopathies; Denmark; DNA-Cytosine Methylases; Heterozygote; Humans; Methionine; Molecular Sequence Data; Mutation; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Prealbumin | 1992 |
Hereditary amyloidosis and cardiomyopathy.
Topics: Amyloidosis; Cardiomyopathies; Genes, Dominant; Humans; Methionine; Mutation; Prealbumin | 1992 |
A Danish kindred with familial amyloid cardiomyopathy revisited: identification of a mutant transthyretin-methionine111 variant in serum from patients and carriers.
Topics: Adult; Aged; Aged, 80 and over; Amyloidosis; Cardiomyopathies; Denmark; Electrophoresis, Polyacrylamide Gel; Female; Heterozygote; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Peptide Fragments; Prealbumin; Sodium Dodecyl Sulfate | 1992 |
Glycosaminoglycans in extracts of cardiac amyloid fibrils from familial amyloid cardiomyopathy of Danish origin related to variant transthyretin Met 111.
Topics: Adult; Amyloidosis; Cardiomyopathies; Chromatography, Gel; Chromatography, Ion Exchange; Denmark; Glycosaminoglycans; Humans; Methionine; Polysaccharides; Prealbumin; Serum Amyloid A Protein | 1991 |
Sarcolemmal phospholipid N-methylation in genetically determined hamster cardiomyopathy.
Topics: Aging; Animals; Cardiomyopathies; Cricetinae; Heart; Kinetics; Mesocricetus; Methionine; Methylation; Myocardium; Phosphatidylethanolamines; Sarcolemma; Species Specificity; Tritium | 1987 |
[The importance of magnesium in preventing myocardial metabolic disorders in thyrotoxicosis].
Topics: Animals; Cardiomyopathies; Glycogen; Hyperthyroidism; Magnesium; Methionine; Myocardium; Phosphocreatine; Rabbits | 1969 |