tyrosine and Amyloidosis, Hereditary

tyrosine has been researched along with Amyloidosis, Hereditary in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hattori, T; Ikeda, S; Kanai, S; Takei, Y; Tokuda, T; Urasawa, N; Yazaki, M	1
Baert-Desurmont, S; Cabot, A; Chastan, N; Dérumeaux, G; Frébourg, T; Hannequin, D; Saugier-Veber, P	1

Other Studies

2 other study(ies) available for tyrosine and Amyloidosis, Hereditary

Article	Year
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
Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene. Muscle & nerve, 2006, Volume: 33, Issue:1 Topics: Aged; Amyloidosis, Familial; Arrhythmias, Cardiac; Aspartic Acid; Facies; France; Gelsolin; Heart Conduction System; Humans; Male; Middle Aged; Pedigree; Point Mutation; Tongue; Tyrosine	2006

Article

Year

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

Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene.

Muscle & nerve, 2006, Volume: 33, Issue:1

Topics: Aged; Amyloidosis, Familial; Arrhythmias, Cardiac; Aspartic Acid; Facies; France; Gelsolin; Heart Conduction System; Humans; Male; Middle Aged; Pedigree; Point Mutation; Tongue; Tyrosine

2006