tryptophan and Cardiomyopathy, Hypertrophic

tryptophan has been researched along with Cardiomyopathy, Hypertrophic in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arai, S; Furutani, Y; Hirayama, K; Imamura, S; Joh-o, K; Kimura, M; Matsuoka, R; Ozawa, T; Sakurai, H; Tamura, M	1
Döhlemann, C; Hebe, J; Meitinger, T; Vosberg, HP	1

Other Studies

2 other study(ies) available for tryptophan and Cardiomyopathy, Hypertrophic

Article	Year
Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy. American journal of medical genetics, 1995, Sep-11, Volume: 58, Issue:3 Topics: Adolescent; Adult; Aged; Base Sequence; Cardiomyopathy, Hypertrophic; Child, Preschool; DNA Primers; Female; Genes, Dominant; Glycine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Myocardium; Myosin Heavy Chains; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Tryptophan	1995
Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the beta-myosin heavy chain gene and cardiac arrest in childhood. A case report and family study. Zeitschrift fur Kardiologie, 2000, Volume: 89, Issue:7 Topics: Arginine; Cardiomyopathy, Hypertrophic; Child; Codon; Death, Sudden, Cardiac; Echocardiography; Electrocardiography; Electrophysiology; Humans; Male; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Tryptophan	2000

Article

Year

Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy.

American journal of medical genetics, 1995, Sep-11, Volume: 58, Issue:3

Topics: Adolescent; Adult; Aged; Base Sequence; Cardiomyopathy, Hypertrophic; Child, Preschool; DNA Primers; Female; Genes, Dominant; Glycine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Myocardium; Myosin Heavy Chains; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Tryptophan

1995

Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the beta-myosin heavy chain gene and cardiac arrest in childhood. A case report and family study.

Zeitschrift fur Kardiologie, 2000, Volume: 89, Issue:7

Topics: Arginine; Cardiomyopathy, Hypertrophic; Child; Codon; Death, Sudden, Cardiac; Echocardiography; Electrocardiography; Electrophysiology; Humans; Male; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Tryptophan

2000