aspartic acid has been researched along with Atrophy, Muscular, Peroneal in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Nave, KA; Werner, HB | 1 |
| Komaki, H; Saito, Y; Sasaki, M; Takashima, H; Yonekawa, T | 1 |
| Hayasaka, K; Kanai, M; Kijima, K; Matsuki, T; Numakura, C; Shirahata, E; Yamashita, S | 1 |
| Floroskufi, P; Kalfakis, N; Karadima, G; Panas, M; Vassilopoulos, D | 1 |
| Angiari, C; Cabrini, I; Cavallaro, T; Fabrizi, GM; Morini, A; Orrico, D; Pellegrini, M; Rizzuto, N; Taioli, F | 1 |
| Barberini, L; Cherchi, MV; Cocco, E; Corongiu, D; Mallarini, G; Marrosu, G; Marrosu, MG; Mura, M; Murru, MR; Tranquilli, S; Vannelli, A | 1 |
| Gal-On, NS; Navon, R; Sadeh, M; Seifried, B | 1 |
1 review(s) available for aspartic acid and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
Myelination of the nervous system: mechanisms and functions.
Topics: Adenosine Triphosphate; Animals; Aspartic Acid; Axons; Central Nervous System; Charcot-Marie-Tooth Disease; Cytoskeleton; Demyelinating Diseases; Glucose; Humans; Inflammation; Leukoencephalopathies; Mice; Microscopy, Electron; Myelin Proteins; Myelin Sheath; Neuronal Plasticity; Oligodendroglia; Peripheral Nervous System; Schwann Cells; Synaptic Transmission | 2014 |
6 other study(ies) available for aspartic acid and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
Congenital hypomyelinating neuropathy attributable to a de novo p.Asp61Asn mutation of the myelin protein zero gene.
Topics: Asparagine; Aspartic Acid; Charcot-Marie-Tooth Disease; Child, Preschool; Humans; Male; Myelin P0 Protein; Sural Nerve | 2013 |
Screening of the early growth response 2 gene in Japanese patients with Charcot-Marie-Tooth disease type 1.
Topics: Adult; Aspartic Acid; Charcot-Marie-Tooth Disease; Connexins; DNA Mutational Analysis; DNA-Binding Proteins; Female; Gap Junction beta-1 Protein; Genetic Carrier Screening; Genetic Testing; Humans; Japan; Male; Molecular Sequence Data; Mutation; Myelin P0 Protein; Myelin Proteins; Trans-Activators; Transcriptional Regulator ERG; Tyrosine | 2003 |
Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variability.
Topics: Adolescent; Adult; Aged; Aspartic Acid; Charcot-Marie-Tooth Disease; Chromosomes, Human, X; Codon, Terminator; Connexins; DNA Mutational Analysis; Family Health; Female; Gap Junction beta-1 Protein; Humans; Leucine; Male; Middle Aged; Mutation; Phenotype; Phenylalanine; Proline; Serine; Tyrosine; Valine | 2006 |
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B.
Topics: Adult; Aged; Aspartic Acid; Charcot-Marie-Tooth Disease; Chromatography, High Pressure Liquid; DNA Mutational Analysis; Exons; Family Health; Female; Gene Dosage; Humans; Male; Microscopy, Electron, Transmission; Molecular Sequence Data; Mutation; Myelin P0 Protein; Nerve Fibers, Myelinated; Pedigree; Protein Structure, Tertiary; Tyrosine | 2006 |
A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities.
Topics: Adolescent; Adult; Aspartic Acid; Brain Chemistry; Brain Stem; Charcot-Marie-Tooth Disease; Connexins; Creatinine; DNA Mutational Analysis; Evoked Potentials; Female; Gap Junction beta-1 Protein; Genetic Diseases, X-Linked; Genetic Predisposition to Disease; Genetic Testing; Humans; Lateral Ventricles; Linkage Disequilibrium; Magnetic Resonance Spectroscopy; Mutation, Missense; Nerve Fibers, Myelinated; Neural Conduction; Neural Pathways; Pedigree; Telencephalon | 2006 |
A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease.
Topics: Amino Acid Sequence; Arginine; Aspartic Acid; Base Sequence; Charcot-Marie-Tooth Disease; Child; Chromosome Mapping; Chromosomes, Human, Pair 17; DNA; Exons; Female; Genetic Carrier Screening; Genetic Markers; Glycine; Humans; Leucine; Male; Molecular Sequence Data; Multigene Family; Myelin Proteins; Pedigree; Point Mutation | 1996 |