Page last updated: 2024-08-17

lysine and Fabry Disease

lysine has been researched along with Fabry Disease in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kajita, M; Miyazaki, T; Mizutani, N; Murata, Y; Niwa, T; Ohmori, S; Seo, H1
Gardner, LI1

Reviews

1 review(s) available for lysine and Fabry Disease

ArticleYear
Genetically expressed abnormalities in the fetus.
    Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3

    Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12

1974

Other Studies

1 other study(ies) available for lysine and Fabry Disease

ArticleYear
A novel mutation (E358K) in the alpha-galactosidase A gene detected in a Japanese family with Fabry disease.
    Human mutation, 1998, Volume: Suppl 1

    Topics: Adolescent; Adult; alpha-Galactosidase; Amino Acid Substitution; Base Sequence; DNA; DNA Mutational Analysis; Fabry Disease; Family Health; Female; Glutamic Acid; Humans; Japan; Lysine; Male; Mutation; Pedigree; Point Mutation

1998