histidine has been researched along with Demyelinating Diseases in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Bhattacharya, SK; Harvey, FC; Hayter, C; Valdivia, AO | 1 |
Ammar, N; Amouri, R; Barisić, N; Ceuterick, C; De Jonghe, P; Hentati, F; Martin, JJ; Merlini, L; Nelis, E; Timmerman, V | 1 |
Brenner, C; Di Rocco, M; Leegwater, PA; Pronk, JC; Salvi, F; Storey, E; van Berkel, CG; van der Knaap, MS | 1 |
3 other study(ies) available for histidine and Demyelinating Diseases
Article | Year |
---|---|
Isobaric Incorporation of C13-Histidine for the Assessment of Remyelination.
Topics: Animals; Axons; Demyelinating Diseases; Disease Models, Animal; Histidine; Humans; Myelin Proteins; Myelin Sheath; Oligodendroglia; Remyelination | 2023 |
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 |
Arg113His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults.
Topics: Adult; Arginine; Brain; Brain Diseases; Demyelinating Diseases; Disease Progression; DNA Mutational Analysis; Eukaryotic Initiation Factor-2B; Female; Follow-Up Studies; Histidine; Homozygote; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation | 2004 |