glutamic acid has been researched along with Amyloidosis, Hereditary 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 | 1 (25.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bollati, M; de Rosa, M; Drnovšek-Olup, B; Fakin, A; Gornik, A; Hawlina, M; Hočevar, A; Jaklič, H; Maver, A; Peterlin, B; Pfeifer, V; Pižem, J; Potrč, M; Teran, N; Vogelnik, K; Volk, M | 1 |
| Bizzi, A; Bugiani, O; Capobianco, R; Carella, F; Cupidi, C; Di Fede, G; Giaccone, G; Giovagnoli, A; Magoni, M; Mangieri, M; Marcon, G; Mazzoleni, G; Morbin, M; Padovani, A; Patruno, GM; Puoti, G; Romorini, A; Rossi, G; Salmaggi, A; Tagliavini, F | 1 |
| Benson, MD; Connors, LH; Skinner, M; Yamashita, T; Yazaki, M | 1 |
| Chan, SC; Chang, CM; Fan, ST; Kwong, YL; Lam, CW; Lau, YK; Lo, CM; Mak, CM; Tam, S; U, LS | 1 |
4 other study(ies) available for glutamic acid and Amyloidosis, Hereditary
| Article | Year |
|---|---|
Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel
Topics: Adult; Aged; Amyloid Neuropathies, Familial; Amyloidosis; Amyloidosis, Familial; Corneal Diseases; Corneal Dystrophies, Hereditary; Exome; Family Health; Female; Fundus Oculi; Gelsolin; Genetic Association Studies; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Mutation; Optic Nerve; Optic Nerve Diseases; Phenotype; Protein Folding; Tomography, Optical Coherence | 2021 |
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
Topics: Aged; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Amyloidosis, Familial; Apolipoprotein E4; Cerebral Hemorrhage; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Italy; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Peptide Fragments | 2010 |
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
Topics: Amino Acid Substitution; Amyloidosis, Familial; Aspartic Acid; Cardiomyopathies; Exons; Glutamic Acid; Humans; Male; Mass Spectrometry; Middle Aged; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Prealbumin | 2004 |
Identification of a novel TTR Gly67Glu mutant and the first case series of familial transthyretin amyloidosis in Hong Kong Chinese.
Topics: Adult; Aged; Amino Acid Substitution; Amyloidosis, Familial; Asian People; DNA Mutational Analysis; Female; Glutamic Acid; Glycine; Hong Kong; Humans; Male; Middle Aged; Mutation; Pedigree; Prealbumin | 2007 |