histidine has been researched along with Peripheral Nerve Diseases in 5 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 | 2 (40.00) | 24.3611 |
| 2020's | 3 (60.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdul-Rahman, OA; Almpani, K; Antony, JH; Barry, BJ; Brewer, C; Chan, WM; Collins, FS; Delaney, A; Engle, EC; Facio, FM; FitzGibbon, EJ; Hunter, DG; Jabs, EW; King, KA; Kvarnung, M; Larsen, DA; Lee, JS; Lee, PR; Lehky, TJ; Ma, A; Maarup, TJ; MacKinnon, S; Manoli, I; Moller, HU; Paul, SM; Ragnhild, G; Robson, CD; Tham, E; Thurm, A; Toro, C; Troedson, C; Van Ryzin, C; Webb, BD; Whitman, MC; Wirgenes, KV; Zalewski, C | 1 |
| 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 |
| Hayes, DF; Henry, NL; Hertz, DL; Kim, JH; Smith, EML; Stringer, KA; Sun, Y; Vangipuram, K; Yeomans, L | 1 |
2 review(s) available for histidine and Peripheral Nerve Diseases
| 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 |
3 other study(ies) available for histidine and Peripheral Nerve Diseases
| Article | Year |
|---|---|
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.
Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Facial Paralysis; Female; Fibrosis; Histidine; Humans; Infant; Male; Mutation; Ophthalmoplegia; Peripheral Nervous System Diseases; Syndrome; Tubulin; Young Adult | 2021 |
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 |
Pharmacometabolomics reveals a role for histidine, phenylalanine, and threonine in the development of paclitaxel-induced peripheral neuropathy.
Topics: Adult; Aged; Biomarkers; Breast Neoplasms; Female; Histidine; Humans; Magnetic Resonance Spectroscopy; Metabolomics; Middle Aged; Paclitaxel; Peripheral Nervous System Diseases; Phenylalanine; Threonine | 2018 |