aspartic acid has been researched along with Alexander Disease in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Namekawa, M; Nishimura, Y; Wada, Y; Yanagihara, C | 1 |
| Brockmann, K; Dechent, P; Frahm, J; Hanefeld, F; Haupt, M; Meins, M; Sperner, J; Stephani, U | 1 |
| Funatsuka, M; Hattori, N; Ishigaki, K; Ito, Y; Kodaira, K; Nakano, K; Osawa, M; Saito, K; Sawaishi, Y | 1 |
| Barker, PB; Bizzi, A; Bugiani, M; Castelli, G; Danesi, U; Erbetta, A; Farina, L; Herskovits, EH; Moroni, I; Uziel, G | 1 |
4 other study(ies) available for aspartic acid and Alexander Disease
| Article | Year |
|---|---|
Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement.
Topics: Adult; Alexander Disease; Asparagine; Aspartic Acid; Basal Ganglia; DNA Mutational Analysis; Family Health; Female; Glial Fibrillary Acidic Protein; Humans; Japan; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Tomography, X-Ray Computed | 2013 |
Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease.
Topics: Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Demyelinating Diseases; Disease Progression; Female; Gliosis; Humans; Infant; Inositol; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Nerve Degeneration; Radiography | 2003 |
TRH therapy in a patient with juvenile Alexander disease.
Topics: Alexander Disease; Aspartic Acid; Child; DNA Mutational Analysis; Female; Glial Fibrillary Acidic Protein; Humans; Magnetic Resonance Imaging; Mutation; Thyrotropin-Releasing Hormone; Valine | 2006 |
Classification of childhood white matter disorders using proton MR spectroscopic imaging.
Topics: Adrenoleukodystrophy; Adult; Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatine; Diagnosis, Differential; DNA Mutational Analysis; Dominance, Cerebral; Female; Hereditary Central Nervous System Demyelinating Diseases; Humans; Image Processing, Computer-Assisted; Infant; Intracellular Signaling Peptides and Proteins; Lactic Acid; Linear Models; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Membrane Proteins; Mitochondrial Diseases; Muscular Dystrophies; Pelizaeus-Merzbacher Disease; Prospective Studies | 2008 |