lysine has been researched along with Amyloid Neuropathy Type 1 in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 1 (14.29) | 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 |
| Alves, A; Braga, C; Cordeiro, Y; Cortines, J; Foguel, D; Graña-Montes, R; Pimenta, KM; Sant'Anna, R; Varejão, N; Ventura, S | 1 |
| Berk, JL; Brannagan, TH; Maurer, MS; Ruzhansky, K; Scoon, J; Weimer, LH | 1 |
| Iida, H; Kobayashi, F; Miwa, M; Nagasaka, K; Nagasaka, T; Nakamura, Y; Shindo, K; Shiozawa, Z; Togashi, S; Watanabe, H | 1 |
| Meredith, SC; Orgel, JP; Sciarretta, KL; Tycko, R | 1 |
| Balan, V; Brandhagen, DJ; Douglas, DD; Mulligan, DC; Perri, RE; Rakela, J; Rosen, CB; Sharma, P; Sirven, JE; Wiesner, RH; Zeldenrust, SR | 1 |
| Iijima, H; Imai, M; Imasawa, M; Sakurada, Y; Toda, Y | 1 |
7 other study(ies) available for lysine and Amyloid Neuropathy Type 1
| 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 |
The importance of a gatekeeper residue on the aggregation of transthyretin: implications for transthyretin-related amyloidoses.
Topics: Amyloid; Amyloid Neuropathies, Familial; Gene Expression; Heparin; Humans; Leucine; Lysine; Mutation; Prealbumin; Protein Aggregation, Pathological; Protein Multimerization; Protein Stability; Protein Structure, Secondary; Protein Structure, Tertiary; Recombinant Proteins; Static Electricity | 2014 |
Discordant phenotype in monozygotic female twins with Lys35Thr TTR familial amyloidotic polyneuropathy.
Topics: Amyloid Neuropathies, Familial; Female; Humans; Lysine; Middle Aged; Phenotype; Prealbumin; Threonine; Twins, Monozygotic | 2014 |
Clinical and histopathological features of progressive-type familial amyloidotic polyneuropathy with TTR Lys54.
Topics: 3-Iodobenzylguanidine; Adult; Amyloid Neuropathies, Familial; Autopsy; Disease Progression; Female; Glucose Tolerance Test; Humans; Lysine; Male; Mutation; Myocardial Perfusion Imaging; Peripheral Nerves; Prealbumin; Sural Nerve | 2009 |
Evidence for novel beta-sheet structures in Iowa mutant beta-amyloid fibrils.
Topics: Amyloid; Amyloid beta-Peptides; Amyloid Neuropathies, Familial; Aspartic Acid; Benzothiazoles; Glutamic Acid; Humans; Kinetics; Leucine; Lysine; Microscopy, Electron, Transmission; Models, Molecular; Mutation, Missense; Nuclear Magnetic Resonance, Biomolecular; Peptide Fragments; Phenylalanine; Protein Structure, Secondary; Spectrometry, Fluorescence; Thiazoles; X-Ray Diffraction | 2009 |
Outcome of liver transplantation for familial amyloidotic polyneuropathy.
Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Diarrhea; Female; Glycine; Humans; Liver Transplantation; Lysine; Male; Methionine; Middle Aged; Mutation; Prealbumin; Treatment Outcome; Tyrosine; Valine | 2003 |
Vitreous opacities in a case of familial amyloidotic polyneuropathy associated with a transthyretin Lys 54.
Topics: Adult; Amyloid Neuropathies, Familial; Eye Diseases; Female; Humans; Lysine; Prealbumin; Vitreous Body | 2004 |