tryptophan has been researched along with Atrophy, Muscular, Peroneal in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 4 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bolon, B; Price, J; Rebelo, AP; Silva, JP; Strickland, AV; Wen, R; Zhang, F; Züchner, S | 1 |
| Beręsewicz, M; Boratyńska-Jasińska, A; Charzewski, Ł; Kabzińska, D; Kawalec, M; Kochański, A; Krzyśko, KA; Zabłocka, B | 1 |
| Bataller, L; Chumillas, MJ; Espinós, C; Martínez-Rubio, D; Mas, F; Mayordomo, F; Muelas, N; Palau, F; Sevilla, T; Sivera, R; Vílchez, JJ | 1 |
| Choi, BO; Choi, KG; Chung, HK; Chung, KW; Hyun, YS; Koo, H; Koo, SK; Lee, HJ; Park, KD; Park, MH; Woo, HM | 1 |
| Ammar, N; Amouri, R; Barisić, N; Ceuterick, C; De Jonghe, P; Hentati, F; Martin, JJ; Merlini, L; Nelis, E; Timmerman, V | 1 |
| Cabrera, VM; Gonzalez, A; Lavilla, NR; Montón, FI; Oterino, A; Pinto, F | 1 |
6 other study(ies) available for tryptophan and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
Characterization of the mitofusin 2 R94W mutation in a knock-in mouse model.
Topics: Animals; Animals, Newborn; Arginine; Cells, Cultured; Charcot-Marie-Tooth Disease; Disease Models, Animal; Escape Reaction; Exploratory Behavior; Fibroblasts; GTP Phosphohydrolases; Humans; In Vitro Techniques; Mice; Mice, Transgenic; Mitochondria; Mitochondrial Proteins; Motor Activity; Muscle Strength; Oxygen Consumption; Point Mutation; Psychomotor Performance; Tryptophan | 2014 |
The Effect of a Novel c.820C>T (Arg274Trp) Mutation in the Mitofusin 2 Gene on Fibroblast Metabolism and Clinical Manifestation in a Patient.
Topics: Amino Acid Substitution; Arginine; Case-Control Studies; Cells, Cultured; Charcot-Marie-Tooth Disease; Fibroblasts; GTP Phosphohydrolases; Humans; Male; Mitochondrial Proteins; Mutation, Missense; Polymorphism, Single Nucleotide; Tryptophan; Young Adult | 2017 |
Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Axons; Charcot-Marie-Tooth Disease; Female; Genes, Dominant; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Nerve Tissue Proteins; Pedigree; Phenotype; Tryptophan; Young Adult | 2010 |
Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2.
Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; Charcot-Marie-Tooth Disease; Child; Child, Preschool; DNA Mutational Analysis; Female; Genetic Linkage; GTP-Binding Protein gamma Subunits; Humans; Male; Mutation, Missense; Pedigree; Phenotype; Republic of Korea; Serine; Tryptophan; Young Adult | 2013 |
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Analysis; Electrophysiology; Family Health; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Male; Microscopy, Electron; Mutation; Nerve Tissue Proteins; Neural Conduction; Pedigree; Peripheral Nerves; Sequence Analysis, DNA; Tryptophan | 2003 |
Arginine-164-tryptophan substitution in connexin32 associated with X linked dominant Charcot-Marie-Tooth disease.
Topics: Arginine; Base Sequence; Charcot-Marie-Tooth Disease; Connexins; DNA Primers; Female; Gap Junction beta-1 Protein; Genes, Dominant; Humans; Male; Molecular Sequence Data; Pedigree; Phenotype; Tryptophan; X Chromosome | 1996 |