Compounds > arginine

arginine and Amyloidosis, Hereditary

arginine has been researched along with Amyloidosis, Hereditary in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (75.00)	29.6817
2010's	1 (25.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cortés-González, V; Kheir, V; Schorderet, DF; Zenteno, JC	1
Barats, MS; Benson, MD; Cohen, AH; Liepnieks, JJ; Yazaki, M	1
Ferlini, A; Grazi, GL; Jovine, E; Mascalchi, M; Pastorelli, F; Plasmati, R; Salvi, F; Tassinari, CA	1
Angus, PW; Brennan, SO; Hawkins, PN; Macdonell, RA; Testro, AG	1

Other Studies

4 other study(ies) available for arginine and Amyloidosis, Hereditary

Article	Year
Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies. Human mutation, 2019, Volume: 40, Issue:6 Topics: Amyloidosis, Familial; Arginine; Corneal Dystrophies, Hereditary; Databases, Genetic; Extracellular Matrix Proteins; Female; Genetic Predisposition to Disease; Humans; Male; Mutation; Pedigree; Phenotype; Transforming Growth Factor beta; Web Browser	2019
Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg. Kidney international, 2003, Volume: 64, Issue:1 Topics: Amino Acid Sequence; Amyloidosis, Familial; Apolipoprotein A-II; Arginine; Base Sequence; Blotting, Western; Codon, Terminator; Cytosine; DNA; Echocardiography; Genetic Variation; Humans; Kidney Diseases; Male; Middle Aged; Molecular Sequence Data; Mutation; Radionuclide Imaging; Rectum; Thymine	2003
Early onset aggressive hereditary amyloidosis: report of an Italian family with TTR Arg47 mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2005, Volume: 26, Issue:2 Topics: Adolescent; Adult; Age of Onset; Amyloidosis, Familial; Arginine; DNA Mutational Analysis; Family Health; Female; Humans; Italy; Male; Mutation; Prealbumin	2005
Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: outcome of hepatorenal transplantation. Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2007, Volume: 13, Issue:7 Topics: Adult; Amino Acid Substitution; Amyloidosis, Familial; Apolipoprotein A-I; Arginine; Genetic Variation; Glycine; Humans; Kidney Transplantation; Liver Transplantation; Male; Mutation; Neural Conduction; Pedigree; Peripheral Nervous System Diseases; Sural Nerve; Tibial Nerve; Treatment Outcome	2007