Compounds > methionine
Page last updated: 2024-08-17

methionine and Congenital Hypothyroidism

methionine has been researched along with Congenital Hypothyroidism in 2 studies

Research

Studies (2)

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

Authors

AuthorsStudies
Liu, L; Liu, S; Lu, D; Niu, X; Xia, H; Yan, S1
Hirayama, M; Irie, M; Nakajima, H; Suwa, S; Wada, Y1

Other Studies

2 other study(ies) available for methionine and Congenital Hypothyroidism

ArticleYear
A novel missense mutation (I26M) in DUOXA2 causing congenital goiter hypothyroidism impairs NADPH oxidase activity but not protein expression.
    The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:4

    Topics: Amino Acid Substitution; Base Sequence; Child; Child, Preschool; Congenital Hypothyroidism; Enzyme Activation; Female; Goiter; Humans; Hydrogen Peroxide; Isoleucine; Male; Membrane Proteins; Methionine; Molecular Sequence Data; Mutation, Missense; NADPH Oxidases

2015
Newborn mass screening in Japan--1984.
    Jinrui idengaku zasshi. The Japanese journal of human genetics, 1984, Volume: 29, Issue:3

    Topics: Congenital Hypothyroidism; Genetic Diseases, Inborn; Genetic Testing; Humans; Hypothyroidism; Infant, Newborn; Japan; Mass Screening; Metabolism, Inborn Errors; Methionine

1984