arginine has been researched along with Adult Pelizaeus-Merzbacher Disease in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abrams, CK; Farina, L; Flores-Obando, R; Freidin, MM; Lamantea, E; Pareyson, D; Salsano, E; Scaioli, V; Scherer, SS; Wong, S | 1 |
Natowicz, MR; Rudick, RA; Staugaitis, SM; Warshawsky, I | 1 |
2 other study(ies) available for arginine and Adult Pelizaeus-Merzbacher Disease
Article | Year |
---|---|
A new mutation in GJC2 associated with subclinical leukodystrophy.
Topics: Adult; Arginine; Brain; Cell Line, Transformed; Connexins; DNA Mutational Analysis; Electroencephalography; Evoked Potentials, Visual; Female; Green Fluorescent Proteins; Humans; Leucine; Magnetic Resonance Imaging; Membrane Potentials; Mutation; Patch-Clamp Techniques; Pelizaeus-Merzbacher Disease; Transfection | 2014 |
Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutation.
Topics: Arginine; Brain; Child; DNA Mutational Analysis; Female; Humans; Leucine; Magnetic Resonance Imaging; Male; Membrane Proteins; Middle Aged; Multiple Sclerosis, Chronic Progressive; Mutation; Myelin Proteolipid Protein; Pelizaeus-Merzbacher Disease; Phenotype | 2005 |