glycine 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 | 4 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auw-Haedrich, C | 1 |
| Agostini, H | 1 |
| Clausen, I | 1 |
| Reinhard, T | 1 |
| Eberwein, P | 1 |
| Schorderet, DF | 1 |
| Gruenauer-Kloevekorn, C | 1 |
| Magy, N | 1 |
| Valleix, S | 1 |
| Grateau, G | 1 |
| Algros, MP | 1 |
| Guillemain, R | 1 |
| Kantelip, B | 1 |
| Delpech, M | 1 |
| Dupond, JL | 1 |
| Testro, AG | 1 |
| Brennan, SO | 1 |
| Macdonell, RA | 1 |
| Hawkins, PN | 1 |
| Angus, PW | 1 |
| Mak, CM | 1 |
| Kwong, YL | 1 |
| Lam, CW | 1 |
| Chan, SC | 1 |
| Lo, CM | 1 |
| Fan, ST | 1 |
| Chang, CM | 1 |
| Lau, YK | 1 |
| U, LS | 1 |
| Tam, S | 1 |
4 other studies available for glycine and Amyloidosis, Hereditary
| Article | Year |
|---|---|
A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
Topics: Adult; Aged; Amyloid; Amyloidosis, Familial; Asparagine; Corneal Dystrophies, Hereditary; DNA Mutati | 2009 |
Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.
Topics: Adult; Alanine; Amyloid Neuropathies; Amyloidosis, Familial; Female; France; Glycine; Humans; Male; | 2002 |
Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: outcome of hepatorenal transplantation.
Topics: Adult; Amino Acid Substitution; Amyloidosis, Familial; Apolipoprotein A-I; Arginine; Genetic Variati | 2007 |
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; | 2007 |