leucine has been researched along with Amyloid Neuropathies, Familial in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (44.44) | 29.6817 |
| 2010's | 4 (44.44) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Björkenheim, A; Szabó, B; Sztaniszláv, ÁJ | 1 |
| Alcazar, A; Corral, I; García-Barragán, N; Jiménez-Escrig, A; Martínez-Alonso, E; Martínez-Poles, J; Martínez-Ulloa, PL; Pian, H; Vallejo, 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 |
| Bull, K; Fontana, M; Gandhi, S; Gilbertson, JA; Gillmore, JD; Hawkins, PN; Holton, JL; Jaunmuktane, Z; McColgan, P; Pinney, J; Reilly, MM; Rowczenio, D; Schott, JM; Shah, S; Sheikh, F; Tudor, R; Viegas, S; Werring, DJ; Whelan, CJ | 1 |
| Meredith, SC; Orgel, JP; Sciarretta, KL; Tycko, R | 1 |
| Baldari, S; Di Bella, G; Di Leo, R; Gentile, L; Mazzeo, A; Minutoli, F; Russo, M; Stancanelli, C; Vita, G | 1 |
| Fernandes, R; Palha, JA; Saraiva, MJ; Sousa, MM; Taboada, A; Vieira, P | 1 |
| Hellman, U; Holmgren, G; Jonasson, J; Lundgren, HE; Suhr, OB; Westermark, P | 1 |
| Aebi, U; Cardoso, I; Damas, AM; Goldsbury, CS; Müller, SA; Olivieri, V; Saraiva, MJ; Wirtz, S | 1 |
9 other study(ies) available for leucine and Amyloid Neuropathies, Familial
| Article | Year |
|---|---|
Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation.
Topics: Amyloid Neuropathies, Familial; Benzoxazoles; Combined Modality Therapy; Diagnosis, Differential; Heart Transplantation; Humans; Leucine; Male; Middle Aged; Mutation; Phenylalanine; Prealbumin | 2020 |
A novel ATTR L32V mutation causes familial amyloid polyneuropathy in a Bolivian family.
Topics: Amyloid Neuropathies, Familial; Bolivia; DNA Mutational Analysis; Family Health; Female; Humans; Leucine; Middle Aged; Mutation; Neural Conduction; Prealbumin; Valine | 2017 |
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 |
Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient.
Topics: Adult; Amyloid Neuropathies, Familial; Humans; Leucine; Male; Meninges; Mutation; Nigeria; Proline | 2015 |
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 |
Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset.
Topics: Age of Onset; Aged; Aged, 80 and over; Amyloid Neuropathies, Familial; Autonomic Nervous System Diseases; Biopsy; Cohort Studies; Diphosphonates; Disease Progression; Electromyography; Female; Follow-Up Studies; Hereditary Sensory and Motor Neuropathy; Humans; Leucine; Male; Middle Aged; Muscle Weakness; Mutation; Neurologic Examination; Organotechnetium Compounds; Phenotype; Prealbumin; Radionuclide Imaging; Radiopharmaceuticals | 2012 |
Evidence for early cytotoxic aggregates in transgenic mice for human transthyretin Leu55Pro.
Topics: Amyloid; Amyloid Neuropathies, Familial; Amyloidosis; Animals; Coloring Agents; Congo Red; Genetic Vectors; Humans; Immunohistochemistry; Intestine, Small; Leucine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Microscopy, Immunoelectron; Mutation; Oxidative Stress; Prealbumin; Proline; RNA, Messenger; Skin | 2002 |
A Swedish family with the rare Phe33Leu transthyretin mutation.
Topics: Amyloid Neuropathies, Familial; Carpal Tunnel Syndrome; Female; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Phenotype; Phenylalanine; Prealbumin; Sweden | 2005 |
Transthyretin fibrillogenesis entails the assembly of monomers: a molecular model for in vitro assembled transthyretin amyloid-like fibrils.
Topics: Amyloid Neuropathies, Familial; Humans; Leucine; Microscopy, Atomic Force; Microscopy, Electron; Microscopy, Electron, Scanning; Models, Molecular; Molecular Weight; Plaque, Amyloid; Prealbumin; Proline; Protein Binding; Protein Precursors; Protein Structure, Quaternary; Time Factors | 2002 |