histidine has been researched along with Acquired Neuromyotonia 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Lin, P; Lv, X; Wang, G; Xu, L; Yan, C; Zhang, D | 1 |
| Attarian, S; Behin, A; Beze-Beyrie, P; Bonello-Palot, N; Boyer, A; Campana-Salort, E; Delague, V; Esselin, F; Latour, P; Levy, N; Lia, AS; Magdelaine, C; Morel, V; Querin, G; Stojkovic, T; Walther-Louvier, U | 1 |
| Finzel, BC; Maize, KM; Shah, RM; Strom, AM; Wagner, CR; West, HT | 1 |
2 review(s) available for histidine and Acquired Neuromyotonia
| Article | Year |
|---|---|
A novel mutation in HINT1 gene causes autosomal recessive axonal neuropathy with neuromyotonia, effective treatment with carbamazepine and review of the literature.
Topics: Adolescent; Carbamazepine; Charcot-Marie-Tooth Disease; Histidine; Humans; Isaacs Syndrome; Muscle Cramp; Mutation; Nerve Tissue Proteins; Nucleotides; Peripheral Nervous System Diseases | 2022 |
HINT1 neuropathy: Expanding the genotype and phenotype spectrum.
Topics: Charcot-Marie-Tooth Disease; Genotype; Histidine; Humans; Isaacs Syndrome; Mutation; Nerve Tissue Proteins; Nucleotides; Peripheral Nervous System Diseases; Phenotype | 2022 |
1 other study(ies) available for histidine and Acquired Neuromyotonia
| Article | Year |
|---|---|
Structure and Functional Characterization of Human Histidine Triad Nucleotide-Binding Protein 1 Mutations Associated with Inherited Axonal Neuropathy with Neuromyotonia.
Topics: Amino Acid Sequence; Crystallography, X-Ray; Histidine; Humans; Isaacs Syndrome; Mutant Proteins; Mutation; Nerve Tissue Proteins; Peripheral Nervous System Diseases; Protein Conformation; Sequence Homology | 2018 |