tryptophan has been researched along with Paraplegia in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 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 |
---|---|
Criscuolo, C; De Michele, G; Filla, A; Mancini, P; Perretti, A; Rinaldi, C; Santorelli, FM; Santoro, L; Scarano, V; Tessa, A; Tucci, T | 1 |
Bhargava, KP; Misra, SS; Singh, KS | 1 |
2 other study(ies) available for tryptophan and Paraplegia
Article | Year |
---|---|
The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy.
Topics: Adolescent; Arginine; Child; DNA Mutational Analysis; Family Health; Female; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Male; Membrane Proteins; Mutation; Paraplegia; Peripheral Nervous System Diseases; Tryptophan | 2005 |
Estimation of 5-hydroxytryptamine (5-HT) level in cerebrospinal fluid of patients with intracranial or spinal lesions.
Topics: Cerebrovascular Disorders; Chromatography, Paper; Humans; Hydroxyindoleacetic Acid; Paraplegia; Quadriplegia; Serotonin; Tryptamines; Tryptophan | 1967 |