methionine has been researched along with Acroosteolysis, Giaccai Type in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adams, D; Delpech, M; Grateau, G; Malapert, D; Said, G; Viemont, M | 1 |
| Haettner, E; Holmgren, G; Lundgren, E; Nordenson, I; Sandgren, O; Steen, L | 1 |
2 other study(ies) available for methionine and Acroosteolysis, Giaccai Type
| Article | Year |
|---|---|
Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France.
Topics: Aged; Aged, 80 and over; Amyloidosis; Base Sequence; Electrophoresis, Agar Gel; France; Hereditary Sensory and Autonomic Neuropathies; Humans; Methionine; Middle Aged; Molecular Sequence Data; Oligonucleotides; Point Mutation; Polymerase Chain Reaction; Prealbumin | 1993 |
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Topics: Adult; Amyloidosis; Female; Hereditary Sensory and Autonomic Neuropathies; Hereditary Sensory and Motor Neuropathy; Homozygote; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Prealbumin; Sweden | 1988 |