Compounds > arginine

arginine and Familial Dysalbuminemic Hyperthyroxinemia

arginine has been researched along with Familial Dysalbuminemic Hyperthyroxinemia in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Agostini, M; Bacon, O; Barrett, T; Beck-Peccoz, P; Bignell, M; Bradbury, S; Campi, I; Chatterjee, K; Clark, P; Druce, M; Geoghegan, F; Gurnell, M; Halsall, D; Lyons, G; Moran, C; O'Toole, A; Rajanayagam, O; Schoenmakers, N; Schwabe, J1

Other Studies

1 other study(ies) available for arginine and Familial Dysalbuminemic Hyperthyroxinemia

ArticleYear
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.
    The Journal of clinical endocrinology and metabolism, 2014, Volume: 99, Issue:7

    Topics: Adult; Amino Acid Substitution; Arginine; Child, Preschool; Female; Humans; Hyperthyroxinemia, Familial Dysalbuminemic; Isoleucine; Male; Models, Molecular; Mutation, Missense; Prealbumin; Thyroid Function Tests; Young Adult

2014