threonine has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Floroskufi, P; Karadima, G; Panas, M; Vassilopoulos, D | 1 |
| Ekici, A; Leonardis, L; Peterlin, B; Rautenstrauss, B; Zidar, J | 1 |
2 other study(ies) available for threonine and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
| Article | Year |
|---|---|
New mutation of the MPZ gene in a family with the Dejerine-Sottas disease phenotype.
Topics: Adult; Amino Acid Substitution; DNA Mutational Analysis; Female; Hereditary Sensory and Motor Neuropathy; Humans; Isoleucine; Male; Middle Aged; Mutation, Missense; Myelin P0 Protein; Pedigree; Phenotype; Threonine | 2007 |
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 |