methionine has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 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 |
|---|---|
| Ekici, A; Leonardis, L; Peterlin, B; Rautenstrauss, B; Zidar, J | 1 |
| Haettner, E; Holmgren, G; Lundgren, E; Nordenson, I; Sandgren, O; Steen, L | 1 |
2 other study(ies) available for methionine and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
| Article | Year |
|---|---|
Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation.
Topics: Charcot-Marie-Tooth Disease; Female; Genes, Dominant; Genes, Recessive; Hereditary Sensory and Motor Neuropathy; Humans; Male; Methionine; Myelin Proteins; Pedigree; Point Mutation; Recombination, Genetic; Slovenia; Threonine | 1998 |
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 |