threonine has been researched along with Amyloid Neuropathies, Familial in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Akagami, T; Ando, T; Ando, Y; Hirotani, S; Misumi, Y; Obayashi, K; Shinriki, S; Tasaki, M; Ueda, M; Watanabe, T; Yamashita, T | 1 |
Berk, JL; Brannagan, TH; Maurer, MS; Ruzhansky, K; Scoon, J; Weimer, LH | 1 |
Modrego, P; Moreira, P; Munar-Qués, M; Saraiva, MJ; Viader-Farré, C | 1 |
Hattori, T; Ikeda, S; Kobayashi, S; Kotani, N; Shirasawa, A; Tokuda, T; Yamagata, S; Yamaguchi, S | 1 |
4 other study(ies) available for threonine and Amyloid Neuropathies, Familial
Article | Year |
---|---|
Dominant cardiac type of familial amyloidotic polyneuropathy associated with a novel transthyretin variant Thr59Arg.
Topics: Amyloid Neuropathies, Familial; Arginine; Humans; Male; Middle Aged; Mutation; Prealbumin; Threonine | 2013 |
Discordant phenotype in monozygotic female twins with Lys35Thr TTR familial amyloidotic polyneuropathy.
Topics: Amyloid Neuropathies, Familial; Female; Humans; Lysine; Middle Aged; Phenotype; Prealbumin; Threonine; Twins, Monozygotic | 2014 |
First Spanish family with familial amyloidotic polyneuropathy associated to TTR Thr49Ile mutation.
Topics: Aged; Amyloid Neuropathies, Familial; Autonomic Nervous System; Digestive System; Female; Humans; Isoleucine; Male; Polymorphism, Single-Stranded Conformational; Prealbumin; Spain; Threonine; White People | 2003 |
Transthyretin Thr60Ala Appalachian-type mutation in a Japanese family with familial amyloidotic polyneuropathy.
Topics: Aged; Alanine; Amino Acid Sequence; Amyloid Neuropathies, Familial; Base Sequence; DNA; Female; Humans; Japan; Male; Point Mutation; Prealbumin; Threonine | 2002 |