tyrosine and Carpal Tunnel Syndrome

tyrosine has been researched along with Carpal Tunnel Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hattori, T; Ikeda, S; Kanai, S; Takei, Y; Tokuda, T; Urasawa, N; Yazaki, M1
Benson, MD; Dupond, JL; Gil, H; Kantelip, B; Kluve-Beckerman, B; Liepnieks, JJ; Magy, N1
Ando, M; Endo, Y; Hara, M; Kawai, R; Murakami, T; Tachibana, S; Tanase, S1

Other Studies

3 other study(ies) available for tyrosine and Carpal Tunnel Syndrome

ArticleYear
Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:1

    Topics: Amyloidosis, Familial; Cardiomyopathies; Carpal Tunnel Syndrome; Female; Humans; Isoleucine; Japan; Middle Aged; Mutation; Phenotype; Prealbumin; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Tyrosine

2003
A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:1

    Topics: Aged; Amyloidosis; Base Sequence; Carpal Tunnel Syndrome; Humans; Male; Pedigree; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Polymorphism, Single-Stranded Conformational; Prealbumin; Skin; Tyrosine

2003
Familial carpal tunnel syndrome due to amyloidogenic transthyretin His 114 variant.
    Neurology, 1994, Volume: 44, Issue:2

    Topics: Aged; Amino Acid Sequence; Amyloid; Base Sequence; Carpal Tunnel Syndrome; DNA; DNA Primers; Exons; Female; Genetic Variation; Histidine; Humans; Japan; Male; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Prealbumin; Restriction Mapping; Tyrosine

1994