arginine and Death, Sudden

arginine has been researched along with Death, Sudden in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boney, CM; Charest, NJ; Feuillan, PP; Merino, MJ; Moran, A; Pescovitz, OH; Shenker, A; Spiegel, AM; Van Wyk, JJ; Weinstein, LS	1
Chen, JJ; Cheng, JJ; Ko, YL; Kuan, P; Lien, WP; Liew, CC; Lin, SY; Liou, YC; Tang, TK; Wu, CW	1

Other Studies

2 other study(ies) available for arginine and Death, Sudden

Article	Year
Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS. The Journal of pediatrics, 1993, Volume: 123, Issue:4 Topics: Adolescent; Antisense Elements (Genetics); Arginine; Cyclic AMP; Death, Sudden; Endocrine System Diseases; Female; Fibrous Dysplasia, Polyostotic; GTP-Binding Proteins; Humans; Infant, Newborn; Male; Mosaicism; Mutation; Polymerase Chain Reaction; Risk Factors	1993
Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failure. Human genetics, 1996, Volume: 97, Issue:5 Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Base Sequence; Cardiomyopathy, Hypertrophic; China; Chromosome Mapping; Chromosomes, Human, Pair 14; Cysteine; Death, Sudden; DNA Primers; Family; Female; Genetic Linkage; Heart Failure; Humans; Male; Molecular Sequence Data; Myosin Heavy Chains; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Prognosis; Survival Analysis	1996

Article

Year

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

The Journal of pediatrics, 1993, Volume: 123, Issue:4

Topics: Adolescent; Antisense Elements (Genetics); Arginine; Cyclic AMP; Death, Sudden; Endocrine System Diseases; Female; Fibrous Dysplasia, Polyostotic; GTP-Binding Proteins; Humans; Infant, Newborn; Male; Mosaicism; Mutation; Polymerase Chain Reaction; Risk Factors

1993

Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failure.

Human genetics, 1996, Volume: 97, Issue:5

Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Base Sequence; Cardiomyopathy, Hypertrophic; China; Chromosome Mapping; Chromosomes, Human, Pair 14; Cysteine; Death, Sudden; DNA Primers; Family; Female; Genetic Linkage; Heart Failure; Humans; Male; Molecular Sequence Data; Myosin Heavy Chains; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Prognosis; Survival Analysis

1996